Name: rs570514618
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs570514618

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:78881190-78881208 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₀ / del(T)₇ / del(T)₆ / del…
del(T)₁₀ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / dup(T)₁₉ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂ / ins(T)₂₃ / ins(T)₂₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₀=0.00 (0/96, ALFA)
del(T)₇=0.00 (0/96, ALFA)
del(T)₆=0.00 (0/96, ALFA) (+ 21 more)
del(T)₅=0.00 (0/96, ALFA)
del(T)₄=0.00 (0/96, ALFA)
delTTT=0.00 (0/96, ALFA)
delTT=0.00 (0/96, ALFA)
delT=0.00 (0/96, ALFA)
dupT=0.00 (0/96, ALFA)
dupTT=0.00 (0/96, ALFA)
dupTTT=0.00 (0/96, ALFA)
dup(T)₄=0.00 (0/96, ALFA)
dup(T)₅=0.00 (0/96, ALFA)
dup(T)₆=0.00 (0/96, ALFA)
dup(T)₇=0.00 (0/96, ALFA)
dup(T)₈=0.00 (0/96, ALFA)
dup(T)₉=0.00 (0/96, ALFA)
dup(T)₁₀=0.00 (0/96, ALFA)
dup(T)₁₁=0.00 (0/96, ALFA)
dup(T)₁₂=0.00 (0/96, ALFA)
dup(T)₁₃=0.00 (0/96, ALFA)
dup(T)₁₄=0.00 (0/96, ALFA)
dup(T)₁₅=0.00 (0/96, ALFA)
dup(T)₁₆=0.00 (0/96, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MORF4L1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	96	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
European	Sub	28	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African	Sub	62	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	54	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	2	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	2	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	96	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, dup(T)₁₅=0.00, dup(T)₁₆=0.00
Allele Frequency Aggregator	African	Sub	62	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, dup(T)₁₅=0.00, dup(T)₁₆=0.00
Allele Frequency Aggregator	European	Sub	28	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, dup(T)₁₅=0.00, dup(T)₁₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	2	(T)₁₉=1.0	del(T)₁₀=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0, dup(T)₉=0.0, dup(T)₁₀=0.0, dup(T)₁₁=0.0, dup(T)₁₂=0.0, dup(T)₁₃=0.0, dup(T)₁₄=0.0, dup(T)₁₅=0.0, dup(T)₁₆=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₁₉=1.0	del(T)₁₀=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0, dup(T)₉=0.0, dup(T)₁₀=0.0, dup(T)₁₁=0.0, dup(T)₁₂=0.0, dup(T)₁₃=0.0, dup(T)₁₄=0.0, dup(T)₁₅=0.0, dup(T)₁₆=0.0
Allele Frequency Aggregator	Other	Sub	2	(T)₁₉=1.0	del(T)₁₀=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0, dup(T)₉=0.0, dup(T)₁₀=0.0, dup(T)₁₁=0.0, dup(T)₁₂=0.0, dup(T)₁₃=0.0, dup(T)₁₄=0.0, dup(T)₁₅=0.0, dup(T)₁₆=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₁₉=0	del(T)₁₀=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0, dup(T)₉=0, dup(T)₁₀=0, dup(T)₁₁=0, dup(T)₁₂=0, dup(T)₁₃=0, dup(T)₁₄=0, dup(T)₁₅=0, dup(T)₁₆=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₉=0	del(T)₁₀=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0, dup(T)₉=0, dup(T)₁₀=0, dup(T)₁₁=0, dup(T)₁₂=0, dup(T)₁₃=0, dup(T)₁₄=0, dup(T)₁₅=0, dup(T)₁₆=0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 15	NC_000015.10:g.78881199_78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881202_78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881203_78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881204_78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881205_78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881206_78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881207_78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881208del
GRCh38.p14 chr 15	NC_000015.10:g.78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881207_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881206_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881205_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881204_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881203_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881202_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881201_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881200_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881199_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881198_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881197_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881196_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881195_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881194_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881193_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881192_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881191_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881190_78881208dup
GRCh38.p14 chr 15	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.79173541_79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173544_79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173545_79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173546_79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173547_79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173548_79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173549_79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173550del
GRCh37.p13 chr 15	NC_000015.9:g.79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173549_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173548_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173547_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173546_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173545_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173544_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173543_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173542_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173541_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173540_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173539_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173538_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173537_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173536_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173535_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173534_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173533_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173532_79173550dup
GRCh37.p13 chr 15	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: MORF4L1, mortality factor 4 like 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MORF4L1 transcript variant 3	NM_001265603.2:c.-109-494… NM_001265603.2:c.-109-4942_-109-4933del	N/A	Intron Variant
MORF4L1 transcript variant 4	NM_001265604.2:c.-110+620… NM_001265604.2:c.-110+620_-110+629del	N/A	Intron Variant
MORF4L1 transcript variant 5	NM_001265605.2:c.-110+620… NM_001265605.2:c.-110+620_-110+629del	N/A	Intron Variant
MORF4L1 transcript variant 1	NM_006791.4:c.155+620_155… NM_006791.4:c.155+620_155+629del	N/A	Intron Variant
MORF4L1 transcript variant 2	NM_206839.3:c.155+620_155… NM_206839.3:c.155+620_155+629del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₉=	del(T)₁₀	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	dup(T)₁₉	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂	ins(T)₂₃	ins(T)₂₈
GRCh38.p14 chr 15	NC_000015.10:g.78881190_78881208=	NC_000015.10:g.78881199_78881208del	NC_000015.10:g.78881202_78881208del	NC_000015.10:g.78881203_78881208del	NC_000015.10:g.78881204_78881208del	NC_000015.10:g.78881205_78881208del	NC_000015.10:g.78881206_78881208del	NC_000015.10:g.78881207_78881208del	NC_000015.10:g.78881208del	NC_000015.10:g.78881208dup	NC_000015.10:g.78881207_78881208dup	NC_000015.10:g.78881206_78881208dup	NC_000015.10:g.78881205_78881208dup	NC_000015.10:g.78881204_78881208dup	NC_000015.10:g.78881203_78881208dup	NC_000015.10:g.78881202_78881208dup	NC_000015.10:g.78881201_78881208dup	NC_000015.10:g.78881200_78881208dup	NC_000015.10:g.78881199_78881208dup	NC_000015.10:g.78881198_78881208dup	NC_000015.10:g.78881197_78881208dup	NC_000015.10:g.78881196_78881208dup	NC_000015.10:g.78881195_78881208dup	NC_000015.10:g.78881194_78881208dup	NC_000015.10:g.78881193_78881208dup	NC_000015.10:g.78881192_78881208dup	NC_000015.10:g.78881191_78881208dup	NC_000015.10:g.78881190_78881208dup	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.78881208_78881209insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.79173532_79173550=	NC_000015.9:g.79173541_79173550del	NC_000015.9:g.79173544_79173550del	NC_000015.9:g.79173545_79173550del	NC_000015.9:g.79173546_79173550del	NC_000015.9:g.79173547_79173550del	NC_000015.9:g.79173548_79173550del	NC_000015.9:g.79173549_79173550del	NC_000015.9:g.79173550del	NC_000015.9:g.79173550dup	NC_000015.9:g.79173549_79173550dup	NC_000015.9:g.79173548_79173550dup	NC_000015.9:g.79173547_79173550dup	NC_000015.9:g.79173546_79173550dup	NC_000015.9:g.79173545_79173550dup	NC_000015.9:g.79173544_79173550dup	NC_000015.9:g.79173543_79173550dup	NC_000015.9:g.79173542_79173550dup	NC_000015.9:g.79173541_79173550dup	NC_000015.9:g.79173540_79173550dup	NC_000015.9:g.79173539_79173550dup	NC_000015.9:g.79173538_79173550dup	NC_000015.9:g.79173537_79173550dup	NC_000015.9:g.79173536_79173550dup	NC_000015.9:g.79173535_79173550dup	NC_000015.9:g.79173534_79173550dup	NC_000015.9:g.79173533_79173550dup	NC_000015.9:g.79173532_79173550dup	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.79173550_79173551insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 3	NM_001265603.1:c.-109-4951=	NM_001265603.1:c.-109-4942_-109-4933del	NM_001265603.1:c.-109-4939_-109-4933del	NM_001265603.1:c.-109-4938_-109-4933del	NM_001265603.1:c.-109-4937_-109-4933del	NM_001265603.1:c.-109-4936_-109-4933del	NM_001265603.1:c.-109-4935_-109-4933del	NM_001265603.1:c.-109-4934_-109-4933del	NM_001265603.1:c.-109-4933del	NM_001265603.1:c.-109-4933dup	NM_001265603.1:c.-109-4934_-109-4933dup	NM_001265603.1:c.-109-4935_-109-4933dup	NM_001265603.1:c.-109-4936_-109-4933dup	NM_001265603.1:c.-109-4937_-109-4933dup	NM_001265603.1:c.-109-4938_-109-4933dup	NM_001265603.1:c.-109-4939_-109-4933dup	NM_001265603.1:c.-109-4940_-109-4933dup	NM_001265603.1:c.-109-4941_-109-4933dup	NM_001265603.1:c.-109-4942_-109-4933dup	NM_001265603.1:c.-109-4943_-109-4933dup	NM_001265603.1:c.-109-4944_-109-4933dup	NM_001265603.1:c.-109-4945_-109-4933dup	NM_001265603.1:c.-109-4946_-109-4933dup	NM_001265603.1:c.-109-4947_-109-4933dup	NM_001265603.1:c.-109-4948_-109-4933dup	NM_001265603.1:c.-109-4949_-109-4933dup	NM_001265603.1:c.-109-4950_-109-4933dup	NM_001265603.1:c.-109-4951_-109-4933dup	NM_001265603.1:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTT	NM_001265603.1:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTT	NM_001265603.1:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTTT	NM_001265603.1:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTTTT	NM_001265603.1:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 3	NM_001265603.2:c.-109-4951=	NM_001265603.2:c.-109-4942_-109-4933del	NM_001265603.2:c.-109-4939_-109-4933del	NM_001265603.2:c.-109-4938_-109-4933del	NM_001265603.2:c.-109-4937_-109-4933del	NM_001265603.2:c.-109-4936_-109-4933del	NM_001265603.2:c.-109-4935_-109-4933del	NM_001265603.2:c.-109-4934_-109-4933del	NM_001265603.2:c.-109-4933del	NM_001265603.2:c.-109-4933dup	NM_001265603.2:c.-109-4934_-109-4933dup	NM_001265603.2:c.-109-4935_-109-4933dup	NM_001265603.2:c.-109-4936_-109-4933dup	NM_001265603.2:c.-109-4937_-109-4933dup	NM_001265603.2:c.-109-4938_-109-4933dup	NM_001265603.2:c.-109-4939_-109-4933dup	NM_001265603.2:c.-109-4940_-109-4933dup	NM_001265603.2:c.-109-4941_-109-4933dup	NM_001265603.2:c.-109-4942_-109-4933dup	NM_001265603.2:c.-109-4943_-109-4933dup	NM_001265603.2:c.-109-4944_-109-4933dup	NM_001265603.2:c.-109-4945_-109-4933dup	NM_001265603.2:c.-109-4946_-109-4933dup	NM_001265603.2:c.-109-4947_-109-4933dup	NM_001265603.2:c.-109-4948_-109-4933dup	NM_001265603.2:c.-109-4949_-109-4933dup	NM_001265603.2:c.-109-4950_-109-4933dup	NM_001265603.2:c.-109-4951_-109-4933dup	NM_001265603.2:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTT	NM_001265603.2:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTT	NM_001265603.2:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTTT	NM_001265603.2:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTTTT	NM_001265603.2:c.-109-4933_-109-4932insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 4	NM_001265604.1:c.-110+611=	NM_001265604.1:c.-110+620_-110+629del	NM_001265604.1:c.-110+623_-110+629del	NM_001265604.1:c.-110+624_-110+629del	NM_001265604.1:c.-110+625_-110+629del	NM_001265604.1:c.-110+626_-110+629del	NM_001265604.1:c.-110+627_-110+629del	NM_001265604.1:c.-110+628_-110+629del	NM_001265604.1:c.-110+629del	NM_001265604.1:c.-110+629dup	NM_001265604.1:c.-110+628_-110+629dup	NM_001265604.1:c.-110+627_-110+629dup	NM_001265604.1:c.-110+626_-110+629dup	NM_001265604.1:c.-110+625_-110+629dup	NM_001265604.1:c.-110+624_-110+629dup	NM_001265604.1:c.-110+623_-110+629dup	NM_001265604.1:c.-110+622_-110+629dup	NM_001265604.1:c.-110+621_-110+629dup	NM_001265604.1:c.-110+620_-110+629dup	NM_001265604.1:c.-110+619_-110+629dup	NM_001265604.1:c.-110+618_-110+629dup	NM_001265604.1:c.-110+617_-110+629dup	NM_001265604.1:c.-110+616_-110+629dup	NM_001265604.1:c.-110+615_-110+629dup	NM_001265604.1:c.-110+614_-110+629dup	NM_001265604.1:c.-110+613_-110+629dup	NM_001265604.1:c.-110+612_-110+629dup	NM_001265604.1:c.-110+611_-110+629dup	NM_001265604.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTT	NM_001265604.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTT	NM_001265604.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTT	NM_001265604.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_001265604.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 4	NM_001265604.2:c.-110+611=	NM_001265604.2:c.-110+620_-110+629del	NM_001265604.2:c.-110+623_-110+629del	NM_001265604.2:c.-110+624_-110+629del	NM_001265604.2:c.-110+625_-110+629del	NM_001265604.2:c.-110+626_-110+629del	NM_001265604.2:c.-110+627_-110+629del	NM_001265604.2:c.-110+628_-110+629del	NM_001265604.2:c.-110+629del	NM_001265604.2:c.-110+629dup	NM_001265604.2:c.-110+628_-110+629dup	NM_001265604.2:c.-110+627_-110+629dup	NM_001265604.2:c.-110+626_-110+629dup	NM_001265604.2:c.-110+625_-110+629dup	NM_001265604.2:c.-110+624_-110+629dup	NM_001265604.2:c.-110+623_-110+629dup	NM_001265604.2:c.-110+622_-110+629dup	NM_001265604.2:c.-110+621_-110+629dup	NM_001265604.2:c.-110+620_-110+629dup	NM_001265604.2:c.-110+619_-110+629dup	NM_001265604.2:c.-110+618_-110+629dup	NM_001265604.2:c.-110+617_-110+629dup	NM_001265604.2:c.-110+616_-110+629dup	NM_001265604.2:c.-110+615_-110+629dup	NM_001265604.2:c.-110+614_-110+629dup	NM_001265604.2:c.-110+613_-110+629dup	NM_001265604.2:c.-110+612_-110+629dup	NM_001265604.2:c.-110+611_-110+629dup	NM_001265604.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTT	NM_001265604.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTT	NM_001265604.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTT	NM_001265604.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_001265604.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 5	NM_001265605.1:c.-110+611=	NM_001265605.1:c.-110+620_-110+629del	NM_001265605.1:c.-110+623_-110+629del	NM_001265605.1:c.-110+624_-110+629del	NM_001265605.1:c.-110+625_-110+629del	NM_001265605.1:c.-110+626_-110+629del	NM_001265605.1:c.-110+627_-110+629del	NM_001265605.1:c.-110+628_-110+629del	NM_001265605.1:c.-110+629del	NM_001265605.1:c.-110+629dup	NM_001265605.1:c.-110+628_-110+629dup	NM_001265605.1:c.-110+627_-110+629dup	NM_001265605.1:c.-110+626_-110+629dup	NM_001265605.1:c.-110+625_-110+629dup	NM_001265605.1:c.-110+624_-110+629dup	NM_001265605.1:c.-110+623_-110+629dup	NM_001265605.1:c.-110+622_-110+629dup	NM_001265605.1:c.-110+621_-110+629dup	NM_001265605.1:c.-110+620_-110+629dup	NM_001265605.1:c.-110+619_-110+629dup	NM_001265605.1:c.-110+618_-110+629dup	NM_001265605.1:c.-110+617_-110+629dup	NM_001265605.1:c.-110+616_-110+629dup	NM_001265605.1:c.-110+615_-110+629dup	NM_001265605.1:c.-110+614_-110+629dup	NM_001265605.1:c.-110+613_-110+629dup	NM_001265605.1:c.-110+612_-110+629dup	NM_001265605.1:c.-110+611_-110+629dup	NM_001265605.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTT	NM_001265605.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTT	NM_001265605.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTT	NM_001265605.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_001265605.1:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 5	NM_001265605.2:c.-110+611=	NM_001265605.2:c.-110+620_-110+629del	NM_001265605.2:c.-110+623_-110+629del	NM_001265605.2:c.-110+624_-110+629del	NM_001265605.2:c.-110+625_-110+629del	NM_001265605.2:c.-110+626_-110+629del	NM_001265605.2:c.-110+627_-110+629del	NM_001265605.2:c.-110+628_-110+629del	NM_001265605.2:c.-110+629del	NM_001265605.2:c.-110+629dup	NM_001265605.2:c.-110+628_-110+629dup	NM_001265605.2:c.-110+627_-110+629dup	NM_001265605.2:c.-110+626_-110+629dup	NM_001265605.2:c.-110+625_-110+629dup	NM_001265605.2:c.-110+624_-110+629dup	NM_001265605.2:c.-110+623_-110+629dup	NM_001265605.2:c.-110+622_-110+629dup	NM_001265605.2:c.-110+621_-110+629dup	NM_001265605.2:c.-110+620_-110+629dup	NM_001265605.2:c.-110+619_-110+629dup	NM_001265605.2:c.-110+618_-110+629dup	NM_001265605.2:c.-110+617_-110+629dup	NM_001265605.2:c.-110+616_-110+629dup	NM_001265605.2:c.-110+615_-110+629dup	NM_001265605.2:c.-110+614_-110+629dup	NM_001265605.2:c.-110+613_-110+629dup	NM_001265605.2:c.-110+612_-110+629dup	NM_001265605.2:c.-110+611_-110+629dup	NM_001265605.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTT	NM_001265605.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTT	NM_001265605.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTT	NM_001265605.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_001265605.2:c.-110+629_-110+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 1	NM_006791.3:c.155+611=	NM_006791.3:c.155+620_155+629del	NM_006791.3:c.155+623_155+629del	NM_006791.3:c.155+624_155+629del	NM_006791.3:c.155+625_155+629del	NM_006791.3:c.155+626_155+629del	NM_006791.3:c.155+627_155+629del	NM_006791.3:c.155+628_155+629del	NM_006791.3:c.155+629del	NM_006791.3:c.155+629dup	NM_006791.3:c.155+628_155+629dup	NM_006791.3:c.155+627_155+629dup	NM_006791.3:c.155+626_155+629dup	NM_006791.3:c.155+625_155+629dup	NM_006791.3:c.155+624_155+629dup	NM_006791.3:c.155+623_155+629dup	NM_006791.3:c.155+622_155+629dup	NM_006791.3:c.155+621_155+629dup	NM_006791.3:c.155+620_155+629dup	NM_006791.3:c.155+619_155+629dup	NM_006791.3:c.155+618_155+629dup	NM_006791.3:c.155+617_155+629dup	NM_006791.3:c.155+616_155+629dup	NM_006791.3:c.155+615_155+629dup	NM_006791.3:c.155+614_155+629dup	NM_006791.3:c.155+613_155+629dup	NM_006791.3:c.155+612_155+629dup	NM_006791.3:c.155+611_155+629dup	NM_006791.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTT	NM_006791.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTT	NM_006791.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTT	NM_006791.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_006791.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 1	NM_006791.4:c.155+611=	NM_006791.4:c.155+620_155+629del	NM_006791.4:c.155+623_155+629del	NM_006791.4:c.155+624_155+629del	NM_006791.4:c.155+625_155+629del	NM_006791.4:c.155+626_155+629del	NM_006791.4:c.155+627_155+629del	NM_006791.4:c.155+628_155+629del	NM_006791.4:c.155+629del	NM_006791.4:c.155+629dup	NM_006791.4:c.155+628_155+629dup	NM_006791.4:c.155+627_155+629dup	NM_006791.4:c.155+626_155+629dup	NM_006791.4:c.155+625_155+629dup	NM_006791.4:c.155+624_155+629dup	NM_006791.4:c.155+623_155+629dup	NM_006791.4:c.155+622_155+629dup	NM_006791.4:c.155+621_155+629dup	NM_006791.4:c.155+620_155+629dup	NM_006791.4:c.155+619_155+629dup	NM_006791.4:c.155+618_155+629dup	NM_006791.4:c.155+617_155+629dup	NM_006791.4:c.155+616_155+629dup	NM_006791.4:c.155+615_155+629dup	NM_006791.4:c.155+614_155+629dup	NM_006791.4:c.155+613_155+629dup	NM_006791.4:c.155+612_155+629dup	NM_006791.4:c.155+611_155+629dup	NM_006791.4:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTT	NM_006791.4:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTT	NM_006791.4:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTT	NM_006791.4:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_006791.4:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 2	NM_206839.2:c.155+611=	NM_206839.2:c.155+620_155+629del	NM_206839.2:c.155+623_155+629del	NM_206839.2:c.155+624_155+629del	NM_206839.2:c.155+625_155+629del	NM_206839.2:c.155+626_155+629del	NM_206839.2:c.155+627_155+629del	NM_206839.2:c.155+628_155+629del	NM_206839.2:c.155+629del	NM_206839.2:c.155+629dup	NM_206839.2:c.155+628_155+629dup	NM_206839.2:c.155+627_155+629dup	NM_206839.2:c.155+626_155+629dup	NM_206839.2:c.155+625_155+629dup	NM_206839.2:c.155+624_155+629dup	NM_206839.2:c.155+623_155+629dup	NM_206839.2:c.155+622_155+629dup	NM_206839.2:c.155+621_155+629dup	NM_206839.2:c.155+620_155+629dup	NM_206839.2:c.155+619_155+629dup	NM_206839.2:c.155+618_155+629dup	NM_206839.2:c.155+617_155+629dup	NM_206839.2:c.155+616_155+629dup	NM_206839.2:c.155+615_155+629dup	NM_206839.2:c.155+614_155+629dup	NM_206839.2:c.155+613_155+629dup	NM_206839.2:c.155+612_155+629dup	NM_206839.2:c.155+611_155+629dup	NM_206839.2:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTT	NM_206839.2:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTT	NM_206839.2:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTT	NM_206839.2:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_206839.2:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant 2	NM_206839.3:c.155+611=	NM_206839.3:c.155+620_155+629del	NM_206839.3:c.155+623_155+629del	NM_206839.3:c.155+624_155+629del	NM_206839.3:c.155+625_155+629del	NM_206839.3:c.155+626_155+629del	NM_206839.3:c.155+627_155+629del	NM_206839.3:c.155+628_155+629del	NM_206839.3:c.155+629del	NM_206839.3:c.155+629dup	NM_206839.3:c.155+628_155+629dup	NM_206839.3:c.155+627_155+629dup	NM_206839.3:c.155+626_155+629dup	NM_206839.3:c.155+625_155+629dup	NM_206839.3:c.155+624_155+629dup	NM_206839.3:c.155+623_155+629dup	NM_206839.3:c.155+622_155+629dup	NM_206839.3:c.155+621_155+629dup	NM_206839.3:c.155+620_155+629dup	NM_206839.3:c.155+619_155+629dup	NM_206839.3:c.155+618_155+629dup	NM_206839.3:c.155+617_155+629dup	NM_206839.3:c.155+616_155+629dup	NM_206839.3:c.155+615_155+629dup	NM_206839.3:c.155+614_155+629dup	NM_206839.3:c.155+613_155+629dup	NM_206839.3:c.155+612_155+629dup	NM_206839.3:c.155+611_155+629dup	NM_206839.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTT	NM_206839.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTT	NM_206839.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTT	NM_206839.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTT	NM_206839.3:c.155+629_155+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MORF4L1 transcript variant X1	XM_005254136.1:c.230+611=	XM_005254136.1:c.230+620_230+629del	XM_005254136.1:c.230+623_230+629del	XM_005254136.1:c.230+624_230+629del	XM_005254136.1:c.230+625_230+629del	XM_005254136.1:c.230+626_230+629del	XM_005254136.1:c.230+627_230+629del	XM_005254136.1:c.230+628_230+629del	XM_005254136.1:c.230+629del	XM_005254136.1:c.230+629dup	XM_005254136.1:c.230+628_230+629dup	XM_005254136.1:c.230+627_230+629dup	XM_005254136.1:c.230+626_230+629dup	XM_005254136.1:c.230+625_230+629dup	XM_005254136.1:c.230+624_230+629dup	XM_005254136.1:c.230+623_230+629dup	XM_005254136.1:c.230+622_230+629dup	XM_005254136.1:c.230+621_230+629dup	XM_005254136.1:c.230+620_230+629dup	XM_005254136.1:c.230+619_230+629dup	XM_005254136.1:c.230+618_230+629dup	XM_005254136.1:c.230+617_230+629dup	XM_005254136.1:c.230+616_230+629dup	XM_005254136.1:c.230+615_230+629dup	XM_005254136.1:c.230+614_230+629dup	XM_005254136.1:c.230+613_230+629dup	XM_005254136.1:c.230+612_230+629dup	XM_005254136.1:c.230+611_230+629dup	XM_005254136.1:c.230+629_230+630insTTTTTTTTTTTTTTTTTTTT	XM_005254136.1:c.230+629_230+630insTTTTTTTTTTTTTTTTTTTTT	XM_005254136.1:c.230+629_230+630insTTTTTTTTTTTTTTTTTTTTTT	XM_005254136.1:c.230+629_230+630insTTTTTTTTTTTTTTTTTTTTTTT	XM_005254136.1:c.230+629_230+630insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

71 SubSNP, 45 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40604121	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95664594	Oct 12, 2018 (152)
3	SSIP	ss947346683	Aug 21, 2014 (142)
4	SWEGEN	ss3013598322	Nov 08, 2017 (151)
5	SWEGEN	ss3013598323	Nov 08, 2017 (151)
6	SWEGEN	ss3013598324	Nov 08, 2017 (151)
7	SWEGEN	ss3013598325	Nov 08, 2017 (151)
8	SWEGEN	ss3013598327	Nov 08, 2017 (151)
9	EVA_DECODE	ss3698274536	Jul 13, 2019 (153)
10	EVA_DECODE	ss3698274537	Jul 13, 2019 (153)
11	EVA_DECODE	ss3698274538	Jul 13, 2019 (153)
12	EVA_DECODE	ss3698274539	Jul 13, 2019 (153)
13	EVA_DECODE	ss3698274540	Jul 13, 2019 (153)
14	EVA_DECODE	ss3698274541	Jul 13, 2019 (153)
15	PACBIO	ss3787902307	Jul 13, 2019 (153)
16	PACBIO	ss3792905232	Jul 13, 2019 (153)
17	PACBIO	ss3792905233	Jul 13, 2019 (153)
18	PACBIO	ss3797789812	Jul 13, 2019 (153)
19	PACBIO	ss3797789813	Jul 13, 2019 (153)
20	EVA	ss3834330668	Apr 27, 2020 (154)
21	GNOMAD	ss4292181555	Apr 27, 2021 (155)
22	GNOMAD	ss4292181556	Apr 27, 2021 (155)
23	GNOMAD	ss4292181557	Apr 27, 2021 (155)
24	GNOMAD	ss4292181558	Apr 27, 2021 (155)
25	GNOMAD	ss4292181559	Apr 27, 2021 (155)
26	GNOMAD	ss4292181560	Apr 27, 2021 (155)
27	GNOMAD	ss4292181561	Apr 27, 2021 (155)
28	GNOMAD	ss4292181562	Apr 27, 2021 (155)
29	GNOMAD	ss4292181563	Apr 27, 2021 (155)
30	GNOMAD	ss4292181564	Apr 27, 2021 (155)
31	GNOMAD	ss4292181565	Apr 27, 2021 (155)
32	GNOMAD	ss4292181566	Apr 27, 2021 (155)
33	GNOMAD	ss4292181567	Apr 27, 2021 (155)
34	GNOMAD	ss4292181568	Apr 27, 2021 (155)
35	GNOMAD	ss4292181569	Apr 27, 2021 (155)
36	GNOMAD	ss4292181570	Apr 27, 2021 (155)
37	GNOMAD	ss4292181571	Apr 27, 2021 (155)
38	GNOMAD	ss4292181572	Apr 27, 2021 (155)
39	GNOMAD	ss4292181573	Apr 27, 2021 (155)
40	GNOMAD	ss4292181574	Apr 27, 2021 (155)
41	GNOMAD	ss4292181575	Apr 27, 2021 (155)
42	GNOMAD	ss4292181576	Apr 27, 2021 (155)
43	GNOMAD	ss4292181577	Apr 27, 2021 (155)
44	GNOMAD	ss4292181578	Apr 27, 2021 (155)
45	GNOMAD	ss4292181580	Apr 27, 2021 (155)
46	GNOMAD	ss4292181581	Apr 27, 2021 (155)
47	GNOMAD	ss4292181582	Apr 27, 2021 (155)
48	GNOMAD	ss4292181583	Apr 27, 2021 (155)
49	GNOMAD	ss4292181584	Apr 27, 2021 (155)
50	GNOMAD	ss4292181585	Apr 27, 2021 (155)
51	GNOMAD	ss4292181586	Apr 27, 2021 (155)
52	GNOMAD	ss4292181587	Apr 27, 2021 (155)
53	TOMMO_GENOMICS	ss5217106557	Apr 27, 2021 (155)
54	TOMMO_GENOMICS	ss5217106558	Apr 27, 2021 (155)
55	TOMMO_GENOMICS	ss5217106559	Apr 27, 2021 (155)
56	TOMMO_GENOMICS	ss5217106560	Apr 27, 2021 (155)
57	TOMMO_GENOMICS	ss5217106561	Apr 27, 2021 (155)
58	TOMMO_GENOMICS	ss5217106562	Apr 27, 2021 (155)
59	HUGCELL_USP	ss5492778213	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5492778214	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5492778215	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5492778216	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5771186024	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5771186025	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5771186026	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5771186027	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5771186028	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5771186029	Oct 16, 2022 (156)
69	EVA	ss5828465069	Oct 16, 2022 (156)
70	EVA	ss5828465070	Oct 16, 2022 (156)
71	EVA	ss5828465071	Oct 16, 2022 (156)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474771561 (NC_000015.10:78881189::T 12/64510) Row 474771562 (NC_000015.10:78881189::TT 10/64510) Row 474771563 (NC_000015.10:78881189::TTT 100/64494)...	-	Apr 27, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 75075864 (NC_000015.9:79173531::TTTTTT 3873/16000) Row 75075865 (NC_000015.9:79173531::TTTT 3104/16000) Row 75075866 (NC_000015.9:79173531::TTTTTTT 1100/16000)...	-	Apr 27, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 75075864 (NC_000015.9:79173531::TTTTTT 3873/16000) Row 75075865 (NC_000015.9:79173531::TTTT 3104/16000) Row 75075866 (NC_000015.9:79173531::TTTTTTT 1100/16000)...	-	Apr 27, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 75075864 (NC_000015.9:79173531::TTTTTT 3873/16000) Row 75075865 (NC_000015.9:79173531::TTTT 3104/16000) Row 75075866 (NC_000015.9:79173531::TTTTTTT 1100/16000)...	-	Apr 27, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 75075864 (NC_000015.9:79173531::TTTTTT 3873/16000) Row 75075865 (NC_000015.9:79173531::TTTT 3104/16000) Row 75075866 (NC_000015.9:79173531::TTTTTTT 1100/16000)...	-	Apr 27, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 75075864 (NC_000015.9:79173531::TTTTTT 3873/16000) Row 75075865 (NC_000015.9:79173531::TTTT 3104/16000) Row 75075866 (NC_000015.9:79173531::TTTTTTT 1100/16000)...	-	Apr 27, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 75075864 (NC_000015.9:79173531::TTTTTT 3873/16000) Row 75075865 (NC_000015.9:79173531::TTTT 3104/16000) Row 75075866 (NC_000015.9:79173531::TTTTTTT 1100/16000)...	-	Apr 27, 2021 (155)
110	14KJPN Submission ignored due to conflicting rows: Row 105023128 (NC_000015.10:78881189::TTTT 6313/27064) Row 105023129 (NC_000015.10:78881189::TTTTTTTTTTT 4125/27064) Row 105023130 (NC_000015.10:78881189::TTTTTT 6534/27064)...	-	Oct 16, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 105023128 (NC_000015.10:78881189::TTTT 6313/27064) Row 105023129 (NC_000015.10:78881189::TTTTTTTTTTT 4125/27064) Row 105023130 (NC_000015.10:78881189::TTTTTT 6534/27064)...	-	Oct 16, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 105023128 (NC_000015.10:78881189::TTTT 6313/27064) Row 105023129 (NC_000015.10:78881189::TTTTTTTTTTT 4125/27064) Row 105023130 (NC_000015.10:78881189::TTTTTT 6534/27064)...	-	Oct 16, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 105023128 (NC_000015.10:78881189::TTTT 6313/27064) Row 105023129 (NC_000015.10:78881189::TTTTTTTTTTT 4125/27064) Row 105023130 (NC_000015.10:78881189::TTTTTT 6534/27064)...	-	Oct 16, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 105023128 (NC_000015.10:78881189::TTTT 6313/27064) Row 105023129 (NC_000015.10:78881189::TTTTTTTTTTT 4125/27064) Row 105023130 (NC_000015.10:78881189::TTTTTT 6534/27064)...	-	Oct 16, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 105023128 (NC_000015.10:78881189::TTTT 6313/27064) Row 105023129 (NC_000015.10:78881189::TTTTTTTTTTT 4125/27064) Row 105023130 (NC_000015.10:78881189::TTTTTT 6534/27064)...	-	Oct 16, 2022 (156)
116	ALFA	NC_000015.10 - 78881190	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4292181587	NC_000015.10:78881189:TTTTTTTTTT:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4292181586	NC_000015.10:78881189:TTTTTTT:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4292181585	NC_000015.10:78881189:TTTTTT:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4292181584	NC_000015.10:78881189:TTTTT:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4292181583	NC_000015.10:78881189:TTTT:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4292181582	NC_000015.10:78881189:TTT:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4292181581	NC_000015.10:78881189:TT:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4292181580	NC_000015.10:78881189:T:	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4292181555	NC_000015.10:78881189::T	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss40604121	NT_010194.17:49964107::T	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4292181556	NC_000015.10:78881189::TT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3834330668, ss5828465069	NC_000015.9:79173531::TTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698274536, ss4292181557	NC_000015.10:78881189::TTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3013598327, ss5217106558	NC_000015.9:79173531::TTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698274537, ss4292181558, ss5492778216, ss5771186024	NC_000015.10:78881189::TTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3792905232, ss3797789812	NC_000015.9:79173531::TTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss947346683	NC_000015.9:79173533::TTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698274538, ss4292181559, ss5492778215	NC_000015.10:78881189::TTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3013598325, ss5217106557, ss5828465070	NC_000015.9:79173531::TTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698274539, ss4292181560, ss5492778213, ss5771186026	NC_000015.10:78881189::TTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95664594	NT_010194.17:49964107::TTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3013598322, ss3787902307, ss3792905233, ss3797789813, ss5217106559, ss5828465071	NC_000015.9:79173531::TTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698274540, ss4292181561, ss5492778214, ss5771186027	NC_000015.10:78881189::TTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3013598323	NC_000015.9:79173531::TTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698274541, ss4292181562	NC_000015.10:78881189::TTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3013598324, ss5217106561	NC_000015.9:79173531::TTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181563, ss5771186028	NC_000015.10:78881189::TTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181564	NC_000015.10:78881189::TTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5217106560	NC_000015.9:79173531::TTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181565, ss5771186025	NC_000015.10:78881189::TTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5217106562	NC_000015.9:79173531::TTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181566, ss5771186029	NC_000015.10:78881189::TTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181567	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181568	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181569	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181570	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3645644882	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181571	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181572	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181573	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181574	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181575	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181576	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181577	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4292181578	NC_000015.10:78881189::TTTTTTTTTTT… NC_000015.10:78881189::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:78881189:TTTTTTTTTTTT… NC_000015.10:78881189:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs570514618

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs570514618