Name: rs71091269
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.

rs71091269

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:92219497-92219521 (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)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / 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 / ins(T)₃₀ / ins(T)₄₅
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.2593 (1215/4686, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C1orf146 : 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	4686	TTTTTTTTTTTTTTTTTTTTTTTTT=0.3698	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1099, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.2593, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0205, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.2015, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0188, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0203, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.693548	0.301613	0.004839	32
European	Sub	4548	TTTTTTTTTTTTTTTTTTTTTTTTT=0.3520	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1130, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.2661, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0211, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.2076, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0193, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0209, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.677474	0.317406	0.005119	32
African	Sub	114	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	106	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTT=0.67	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.06, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.28, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.75	0.25	0.0	5

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	4686	(T)₂₅=0.3698	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1099, dupTT=0.2593, dupTTT=0.0205, dup(T)₄=0.2015, dup(T)₅=0.0203, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0188
Allele Frequency Aggregator	European	Sub	4548	(T)₂₅=0.3520	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1130, dupTT=0.2661, dupTTT=0.0211, dup(T)₄=0.2076, dup(T)₅=0.0209, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0193
Allele Frequency Aggregator	African	Sub	114	(T)₂₅=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Other	Sub	18	(T)₂₅=0.67	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=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=0.06, dupTT=0.28, 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
Allele Frequency Aggregator	Latin American 2	Sub	4	(T)₂₅=1.0	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=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
Allele Frequency Aggregator	Latin American 1	Sub	2	(T)₂₅=1.0	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=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
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₅=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=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
Allele Frequency Aggregator	Asian	Sub	0	(T)₂₅=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=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

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 1	NC_000001.11:g.92219509_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219510_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219511_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219512_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219513_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219514_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219515_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219516_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219517_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219518_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219519_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219520_92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219521del
GRCh38.p14 chr 1	NC_000001.11:g.92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219520_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219519_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219518_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219517_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219516_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219515_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219514_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219513_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219512_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219511_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219510_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219509_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219508_92219521dup
GRCh38.p14 chr 1	NC_000001.11:g.92219521_92219522insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.92219521_92219522insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.92685066_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685067_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685068_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685069_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685070_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685071_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685072_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685073_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685074_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685075_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685076_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685077_92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685078del
GRCh37.p13 chr 1	NC_000001.10:g.92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685077_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685076_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685075_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685074_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685073_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685072_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685071_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685070_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685069_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685068_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685067_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685066_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685065_92685078dup
GRCh37.p13 chr 1	NC_000001.10:g.92685078_92685079insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.92685078_92685079insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: C1orf146, chromosome 1 open reading frame 146 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C1orf146 transcript	NM_001012425.2:c.-40+1461… NM_001012425.2:c.-40+1461_-40+1473del	N/A	Intron Variant
C1orf146 transcript variant X1	XM_011541447.3:c.-139+146… XM_011541447.3:c.-139+1461_-139+1473del	N/A	Intron Variant
C1orf146 transcript variant X3	XM_047420086.1:c.-18+1461… XM_047420086.1:c.-18+1461_-18+1473del	N/A	Intron Variant
C1orf146 transcript variant X2	XM_047420085.1:c.	N/A	Genic Upstream Transcript 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)₂₅=	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	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	ins(T)₃₀	ins(T)₄₅
GRCh38.p14 chr 1	NC_000001.11:g.92219497_92219521=	NC_000001.11:g.92219509_92219521del	NC_000001.11:g.92219510_92219521del	NC_000001.11:g.92219511_92219521del	NC_000001.11:g.92219512_92219521del	NC_000001.11:g.92219513_92219521del	NC_000001.11:g.92219514_92219521del	NC_000001.11:g.92219515_92219521del	NC_000001.11:g.92219516_92219521del	NC_000001.11:g.92219517_92219521del	NC_000001.11:g.92219518_92219521del	NC_000001.11:g.92219519_92219521del	NC_000001.11:g.92219520_92219521del	NC_000001.11:g.92219521del	NC_000001.11:g.92219521dup	NC_000001.11:g.92219520_92219521dup	NC_000001.11:g.92219519_92219521dup	NC_000001.11:g.92219518_92219521dup	NC_000001.11:g.92219517_92219521dup	NC_000001.11:g.92219516_92219521dup	NC_000001.11:g.92219515_92219521dup	NC_000001.11:g.92219514_92219521dup	NC_000001.11:g.92219513_92219521dup	NC_000001.11:g.92219512_92219521dup	NC_000001.11:g.92219511_92219521dup	NC_000001.11:g.92219510_92219521dup	NC_000001.11:g.92219509_92219521dup	NC_000001.11:g.92219508_92219521dup	NC_000001.11:g.92219521_92219522insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.92219521_92219522insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.92685054_92685078=	NC_000001.10:g.92685066_92685078del	NC_000001.10:g.92685067_92685078del	NC_000001.10:g.92685068_92685078del	NC_000001.10:g.92685069_92685078del	NC_000001.10:g.92685070_92685078del	NC_000001.10:g.92685071_92685078del	NC_000001.10:g.92685072_92685078del	NC_000001.10:g.92685073_92685078del	NC_000001.10:g.92685074_92685078del	NC_000001.10:g.92685075_92685078del	NC_000001.10:g.92685076_92685078del	NC_000001.10:g.92685077_92685078del	NC_000001.10:g.92685078del	NC_000001.10:g.92685078dup	NC_000001.10:g.92685077_92685078dup	NC_000001.10:g.92685076_92685078dup	NC_000001.10:g.92685075_92685078dup	NC_000001.10:g.92685074_92685078dup	NC_000001.10:g.92685073_92685078dup	NC_000001.10:g.92685072_92685078dup	NC_000001.10:g.92685071_92685078dup	NC_000001.10:g.92685070_92685078dup	NC_000001.10:g.92685069_92685078dup	NC_000001.10:g.92685068_92685078dup	NC_000001.10:g.92685067_92685078dup	NC_000001.10:g.92685066_92685078dup	NC_000001.10:g.92685065_92685078dup	NC_000001.10:g.92685078_92685079insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.92685078_92685079insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
C1orf146 transcript	NM_001012425.1:c.-40+1449=	NM_001012425.1:c.-40+1461_-40+1473del	NM_001012425.1:c.-40+1462_-40+1473del	NM_001012425.1:c.-40+1463_-40+1473del	NM_001012425.1:c.-40+1464_-40+1473del	NM_001012425.1:c.-40+1465_-40+1473del	NM_001012425.1:c.-40+1466_-40+1473del	NM_001012425.1:c.-40+1467_-40+1473del	NM_001012425.1:c.-40+1468_-40+1473del	NM_001012425.1:c.-40+1469_-40+1473del	NM_001012425.1:c.-40+1470_-40+1473del	NM_001012425.1:c.-40+1471_-40+1473del	NM_001012425.1:c.-40+1472_-40+1473del	NM_001012425.1:c.-40+1473del	NM_001012425.1:c.-40+1473dup	NM_001012425.1:c.-40+1472_-40+1473dup	NM_001012425.1:c.-40+1471_-40+1473dup	NM_001012425.1:c.-40+1470_-40+1473dup	NM_001012425.1:c.-40+1469_-40+1473dup	NM_001012425.1:c.-40+1468_-40+1473dup	NM_001012425.1:c.-40+1467_-40+1473dup	NM_001012425.1:c.-40+1466_-40+1473dup	NM_001012425.1:c.-40+1465_-40+1473dup	NM_001012425.1:c.-40+1464_-40+1473dup	NM_001012425.1:c.-40+1463_-40+1473dup	NM_001012425.1:c.-40+1462_-40+1473dup	NM_001012425.1:c.-40+1461_-40+1473dup	NM_001012425.1:c.-40+1460_-40+1473dup	NM_001012425.1:c.-40+1473_-40+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001012425.1:c.-40+1473_-40+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
C1orf146 transcript	NM_001012425.2:c.-40+1449=	NM_001012425.2:c.-40+1461_-40+1473del	NM_001012425.2:c.-40+1462_-40+1473del	NM_001012425.2:c.-40+1463_-40+1473del	NM_001012425.2:c.-40+1464_-40+1473del	NM_001012425.2:c.-40+1465_-40+1473del	NM_001012425.2:c.-40+1466_-40+1473del	NM_001012425.2:c.-40+1467_-40+1473del	NM_001012425.2:c.-40+1468_-40+1473del	NM_001012425.2:c.-40+1469_-40+1473del	NM_001012425.2:c.-40+1470_-40+1473del	NM_001012425.2:c.-40+1471_-40+1473del	NM_001012425.2:c.-40+1472_-40+1473del	NM_001012425.2:c.-40+1473del	NM_001012425.2:c.-40+1473dup	NM_001012425.2:c.-40+1472_-40+1473dup	NM_001012425.2:c.-40+1471_-40+1473dup	NM_001012425.2:c.-40+1470_-40+1473dup	NM_001012425.2:c.-40+1469_-40+1473dup	NM_001012425.2:c.-40+1468_-40+1473dup	NM_001012425.2:c.-40+1467_-40+1473dup	NM_001012425.2:c.-40+1466_-40+1473dup	NM_001012425.2:c.-40+1465_-40+1473dup	NM_001012425.2:c.-40+1464_-40+1473dup	NM_001012425.2:c.-40+1463_-40+1473dup	NM_001012425.2:c.-40+1462_-40+1473dup	NM_001012425.2:c.-40+1461_-40+1473dup	NM_001012425.2:c.-40+1460_-40+1473dup	NM_001012425.2:c.-40+1473_-40+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001012425.2:c.-40+1473_-40+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
C1orf146 transcript variant X1	XM_011541447.3:c.-139+1449=	XM_011541447.3:c.-139+1461_-139+1473del	XM_011541447.3:c.-139+1462_-139+1473del	XM_011541447.3:c.-139+1463_-139+1473del	XM_011541447.3:c.-139+1464_-139+1473del	XM_011541447.3:c.-139+1465_-139+1473del	XM_011541447.3:c.-139+1466_-139+1473del	XM_011541447.3:c.-139+1467_-139+1473del	XM_011541447.3:c.-139+1468_-139+1473del	XM_011541447.3:c.-139+1469_-139+1473del	XM_011541447.3:c.-139+1470_-139+1473del	XM_011541447.3:c.-139+1471_-139+1473del	XM_011541447.3:c.-139+1472_-139+1473del	XM_011541447.3:c.-139+1473del	XM_011541447.3:c.-139+1473dup	XM_011541447.3:c.-139+1472_-139+1473dup	XM_011541447.3:c.-139+1471_-139+1473dup	XM_011541447.3:c.-139+1470_-139+1473dup	XM_011541447.3:c.-139+1469_-139+1473dup	XM_011541447.3:c.-139+1468_-139+1473dup	XM_011541447.3:c.-139+1467_-139+1473dup	XM_011541447.3:c.-139+1466_-139+1473dup	XM_011541447.3:c.-139+1465_-139+1473dup	XM_011541447.3:c.-139+1464_-139+1473dup	XM_011541447.3:c.-139+1463_-139+1473dup	XM_011541447.3:c.-139+1462_-139+1473dup	XM_011541447.3:c.-139+1461_-139+1473dup	XM_011541447.3:c.-139+1460_-139+1473dup	XM_011541447.3:c.-139+1473_-139+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011541447.3:c.-139+1473_-139+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
C1orf146 transcript variant X3	XM_047420086.1:c.-18+1449=	XM_047420086.1:c.-18+1461_-18+1473del	XM_047420086.1:c.-18+1462_-18+1473del	XM_047420086.1:c.-18+1463_-18+1473del	XM_047420086.1:c.-18+1464_-18+1473del	XM_047420086.1:c.-18+1465_-18+1473del	XM_047420086.1:c.-18+1466_-18+1473del	XM_047420086.1:c.-18+1467_-18+1473del	XM_047420086.1:c.-18+1468_-18+1473del	XM_047420086.1:c.-18+1469_-18+1473del	XM_047420086.1:c.-18+1470_-18+1473del	XM_047420086.1:c.-18+1471_-18+1473del	XM_047420086.1:c.-18+1472_-18+1473del	XM_047420086.1:c.-18+1473del	XM_047420086.1:c.-18+1473dup	XM_047420086.1:c.-18+1472_-18+1473dup	XM_047420086.1:c.-18+1471_-18+1473dup	XM_047420086.1:c.-18+1470_-18+1473dup	XM_047420086.1:c.-18+1469_-18+1473dup	XM_047420086.1:c.-18+1468_-18+1473dup	XM_047420086.1:c.-18+1467_-18+1473dup	XM_047420086.1:c.-18+1466_-18+1473dup	XM_047420086.1:c.-18+1465_-18+1473dup	XM_047420086.1:c.-18+1464_-18+1473dup	XM_047420086.1:c.-18+1463_-18+1473dup	XM_047420086.1:c.-18+1462_-18+1473dup	XM_047420086.1:c.-18+1461_-18+1473dup	XM_047420086.1:c.-18+1460_-18+1473dup	XM_047420086.1:c.-18+1473_-18+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047420086.1:c.-18+1473_-18+1474insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

59 SubSNP, 41 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95236605	Feb 13, 2009 (130)
2	HUMANGENOME_JCVI	ss98573432	Apr 25, 2013 (138)
3	PJP	ss294591822	May 31, 2013 (138)
4	SWEGEN	ss2987226171	Nov 08, 2017 (151)
5	MCHAISSO	ss3065314941	Nov 08, 2017 (151)
6	URBANLAB	ss3646720008	Oct 11, 2018 (152)
7	URBANLAB	ss3646720009	Oct 11, 2018 (152)
8	EVA_DECODE	ss3687270243	Jul 12, 2019 (153)
9	EVA_DECODE	ss3687270244	Jul 12, 2019 (153)
10	EVA_DECODE	ss3687270245	Jul 12, 2019 (153)
11	EVA_DECODE	ss3687270246	Jul 12, 2019 (153)
12	EVA_DECODE	ss3687270247	Jul 12, 2019 (153)
13	EVA	ss3826302582	Apr 25, 2020 (154)
14	GNOMAD	ss3998105530	Apr 25, 2021 (155)
15	GNOMAD	ss3998105531	Apr 25, 2021 (155)
16	GNOMAD	ss3998105532	Apr 25, 2021 (155)
17	GNOMAD	ss3998105533	Apr 25, 2021 (155)
18	GNOMAD	ss3998105534	Apr 25, 2021 (155)
19	GNOMAD	ss3998105535	Apr 25, 2021 (155)
20	GNOMAD	ss3998105536	Apr 25, 2021 (155)
21	GNOMAD	ss3998105537	Apr 25, 2021 (155)
22	GNOMAD	ss3998105538	Apr 25, 2021 (155)
23	GNOMAD	ss3998105539	Apr 25, 2021 (155)
24	GNOMAD	ss3998105540	Apr 25, 2021 (155)
25	GNOMAD	ss3998105541	Apr 25, 2021 (155)
26	GNOMAD	ss3998105542	Apr 25, 2021 (155)
27	GNOMAD	ss3998105543	Apr 25, 2021 (155)
28	GNOMAD	ss3998105544	Apr 25, 2021 (155)
29	GNOMAD	ss3998105545	Apr 25, 2021 (155)
30	GNOMAD	ss3998105547	Apr 25, 2021 (155)
31	GNOMAD	ss3998105548	Apr 25, 2021 (155)
32	GNOMAD	ss3998105549	Apr 25, 2021 (155)
33	GNOMAD	ss3998105550	Apr 25, 2021 (155)
34	GNOMAD	ss3998105551	Apr 25, 2021 (155)
35	GNOMAD	ss3998105552	Apr 25, 2021 (155)
36	GNOMAD	ss3998105553	Apr 25, 2021 (155)
37	GNOMAD	ss3998105554	Apr 25, 2021 (155)
38	GNOMAD	ss3998105555	Apr 25, 2021 (155)
39	GNOMAD	ss3998105556	Apr 25, 2021 (155)
40	GNOMAD	ss3998105557	Apr 25, 2021 (155)
41	GNOMAD	ss3998105558	Apr 25, 2021 (155)
42	TOMMO_GENOMICS	ss5145088261	Apr 25, 2021 (155)
43	TOMMO_GENOMICS	ss5145088262	Apr 25, 2021 (155)
44	TOMMO_GENOMICS	ss5145088263	Apr 25, 2021 (155)
45	TOMMO_GENOMICS	ss5145088264	Apr 25, 2021 (155)
46	TOMMO_GENOMICS	ss5145088265	Apr 25, 2021 (155)
47	TOMMO_GENOMICS	ss5145088266	Apr 25, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5243152422	Oct 12, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5243152423	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5444121036	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5444121037	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5444121038	Oct 12, 2022 (156)
53	HUGCELL_USP	ss5444121039	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5670183330	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5670183331	Oct 12, 2022 (156)
56	TOMMO_GENOMICS	ss5670183332	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5670183333	Oct 12, 2022 (156)
58	TOMMO_GENOMICS	ss5670183334	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5670183335	Oct 12, 2022 (156)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18819153 (NC_000001.11:92219496::T 11218/77136) Row 18819154 (NC_000001.11:92219496::TT 35198/76764) Row 18819155 (NC_000001.11:92219496::TTT 3737/77400)...	-	Apr 25, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 3057568 (NC_000001.10:92685053::TT 12300/16214) Row 3057569 (NC_000001.10:92685053::T 447/16214) Row 3057570 (NC_000001.10:92685053::TTTT 665/16214)...	-	Apr 25, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 3057568 (NC_000001.10:92685053::TT 12300/16214) Row 3057569 (NC_000001.10:92685053::T 447/16214) Row 3057570 (NC_000001.10:92685053::TTTT 665/16214)...	-	Apr 25, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 3057568 (NC_000001.10:92685053::TT 12300/16214) Row 3057569 (NC_000001.10:92685053::T 447/16214) Row 3057570 (NC_000001.10:92685053::TTTT 665/16214)...	-	Apr 25, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 3057568 (NC_000001.10:92685053::TT 12300/16214) Row 3057569 (NC_000001.10:92685053::T 447/16214) Row 3057570 (NC_000001.10:92685053::TTTT 665/16214)...	-	Apr 25, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 3057568 (NC_000001.10:92685053::TT 12300/16214) Row 3057569 (NC_000001.10:92685053::T 447/16214) Row 3057570 (NC_000001.10:92685053::TTTT 665/16214)...	-	Apr 25, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 3057568 (NC_000001.10:92685053::TT 12300/16214) Row 3057569 (NC_000001.10:92685053::T 447/16214) Row 3057570 (NC_000001.10:92685053::TTTT 665/16214)...	-	Apr 25, 2021 (155)
94	14KJPN Submission ignored due to conflicting rows: Row 4020434 (NC_000001.11:92219496::TTTT 976/26570) Row 4020435 (NC_000001.11:92219496::TT 19385/26570) Row 4020436 (NC_000001.11:92219496::TTT 569/26570)...	-	Oct 12, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 4020434 (NC_000001.11:92219496::TTTT 976/26570) Row 4020435 (NC_000001.11:92219496::TT 19385/26570) Row 4020436 (NC_000001.11:92219496::TTT 569/26570)...	-	Oct 12, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 4020434 (NC_000001.11:92219496::TTTT 976/26570) Row 4020435 (NC_000001.11:92219496::TT 19385/26570) Row 4020436 (NC_000001.11:92219496::TTT 569/26570)...	-	Oct 12, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 4020434 (NC_000001.11:92219496::TTTT 976/26570) Row 4020435 (NC_000001.11:92219496::TT 19385/26570) Row 4020436 (NC_000001.11:92219496::TTT 569/26570)...	-	Oct 12, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 4020434 (NC_000001.11:92219496::TTTT 976/26570) Row 4020435 (NC_000001.11:92219496::TT 19385/26570) Row 4020436 (NC_000001.11:92219496::TTT 569/26570)...	-	Oct 12, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 4020434 (NC_000001.11:92219496::TTTT 976/26570) Row 4020435 (NC_000001.11:92219496::TT 19385/26570) Row 4020436 (NC_000001.11:92219496::TTT 569/26570)...	-	Oct 12, 2022 (156)
100	ALFA	NC_000001.11 - 92219497	Apr 25, 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
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3998105558	NC_000001.11:92219496:TTTTTTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3998105557	NC_000001.11:92219496:TTTTTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss2987226171	NC_000001.10:92685053:TTTTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3998105556	NC_000001.11:92219496:TTTTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3065314941, ss3998105555	NC_000001.11:92219496:TTTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3998105554	NC_000001.11:92219496:TTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3998105553	NC_000001.11:92219496:TTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3998105552	NC_000001.11:92219496:TTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3998105551	NC_000001.11:92219496:TTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3998105550	NC_000001.11:92219496:TTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105549	NC_000001.11:92219496:TTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105548	NC_000001.11:92219496:TT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105547	NC_000001.11:92219496:T:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5145088262	NC_000001.10:92685053::T	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3687270243, ss3998105530, ss5444121038, ss5670183333	NC_000001.11:92219496::T	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294591822	NC_000001.9:92457642::TT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3826302582, ss5145088261	NC_000001.10:92685053::TT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3687270244, ss3998105531, ss5444121039, ss5670183331	NC_000001.11:92219496::TT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3646720009	NC_000001.11:92219520::TT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss98573432	NT_032977.9:62656992::TT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95236605	NT_032977.9:62656996::TT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5145088264	NC_000001.10:92685053::TTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3687270245, ss3998105532, ss5243152423, ss5670183332	NC_000001.11:92219496::TTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3646720008	NC_000001.11:92219519::TTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5145088263	NC_000001.10:92685053::TTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3687270246, ss3998105533, ss5444121037, ss5670183330	NC_000001.11:92219496::TTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5145088265	NC_000001.10:92685053::TTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3687270247, ss3998105534, ss5243152422, ss5444121036, ss5670183334	NC_000001.11:92219496::TTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5145088266	NC_000001.10:92685053::TTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105535, ss5670183335	NC_000001.11:92219496::TTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105536	NC_000001.11:92219496::TTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105537	NC_000001.11:92219496::TTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11791714590	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105538	NC_000001.11:92219496::TTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105539	NC_000001.11:92219496::TTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105540	NC_000001.11:92219496::TTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105541	NC_000001.11:92219496::TTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105542	NC_000001.11:92219496::TTTTTTTTTTT… NC_000001.11:92219496::TTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105543	NC_000001.11:92219496::TTTTTTTTTTT… NC_000001.11:92219496::TTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105544	NC_000001.11:92219496::TTTTTTTTTTT… NC_000001.11:92219496::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3998105545	NC_000001.11:92219496::TTTTTTTTTTT… NC_000001.11:92219496::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2326945859	NC_000001.10:92685053:TTTTTTTTTTTT… NC_000001.10:92685053:TTTTTTTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT
ss3083325745	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTT:	NC_000001.11:92219496:TTTTTTTTTTTT… NC_000001.11:92219496:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT

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

No publications for rs71091269

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

rs71091269