Name: rs71371255
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.

rs71371255

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:12409160-12409184 (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)₁₂ / del(T)₁₁ / del(T)₉ / de…
del(T)₁₂ / del(T)₁₁ / del(T)₉ / del(T)₈ / del(T)₇ / 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)₁₆ / ins(T)₂₉
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.0893 (609/6816, ALFA)
(T)₂₅=0.33 (13/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PRELID3A : 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	6816	TTTTTTTTTTTTTTTTTTTTTTTTT=0.7789	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0452, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0893, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0662, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0123, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0067, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.884422	0.06066	0.054917	32
European	Sub	6256	TTTTTTTTTTTTTTTTTTTTTTTTT=0.7596	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0491, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0972, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0719, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0134, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0074, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.871611	0.067384	0.061005	32
African	Sub	320	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	302	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	34	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	84	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	102	TTTTTTTTTTTTTTTTTTTTTTTTT=0.971	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.010, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.010, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.010, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	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	6816	(T)₂₅=0.7789	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0452, dupTT=0.0893, dupTTT=0.0662, dup(T)₄=0.0123, dup(T)₅=0.0067, dup(T)₆=0.0013, dup(T)₈=0.0000
Allele Frequency Aggregator	European	Sub	6256	(T)₂₅=0.7596	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0491, dupTT=0.0972, dupTTT=0.0719, dup(T)₄=0.0134, dup(T)₅=0.0074, dup(T)₆=0.0014, dup(T)₈=0.0000
Allele Frequency Aggregator	African	Sub	320	(T)₂₅=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=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)₈=0.000
Allele Frequency Aggregator	Other	Sub	102	(T)₂₅=0.971	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.010, dupTT=0.010, dupTTT=0.010, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Latin American 2	Sub	84	(T)₂₅=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=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)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	34	(T)₂₅=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=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)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(T)₂₅=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=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)₈=0.00
Allele Frequency Aggregator	Asian	Sub	8	(T)₂₅=1.0	del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=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)₈=0.0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupTTT=0.68

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 18	NC_000018.10:g.12409173_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409174_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409176_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409177_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409178_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409180_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409181_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409182_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409183_12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409184del
GRCh38.p14 chr 18	NC_000018.10:g.12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409183_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409182_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409181_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409180_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409179_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409178_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409177_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409176_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409175_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409174_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409173_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409172_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409171_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409169_12409184dup
GRCh38.p14 chr 18	NC_000018.10:g.12409184_12409185insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 18	NC_000018.9:g.12409172_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409173_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409175_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409176_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409177_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409179_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409180_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409181_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409182_12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409183del
GRCh37.p13 chr 18	NC_000018.9:g.12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409182_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409181_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409180_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409179_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409178_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409177_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409176_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409175_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409174_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409173_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409172_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409171_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409170_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409168_12409183dup
GRCh37.p13 chr 18	NC_000018.9:g.12409183_12409184insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: PRELID3A, PRELI domain containing 3A (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PRELID3A transcript variant 1	NM_001142405.2:c.32+1166_… NM_001142405.2:c.32+1166_32+1177del	N/A	Intron Variant
PRELID3A transcript variant 2	NM_006553.4:c.32+1166_32+… NM_006553.4:c.32+1166_32+1177del	N/A	Intron Variant
PRELID3A transcript variant 3	NM_001142406.1:c.	N/A	Genic Upstream Transcript Variant
PRELID3A transcript variant X3	XM_024451075.1:c.44+419_4… XM_024451075.1:c.44+419_44+430del	N/A	Intron Variant
PRELID3A transcript variant X5	XM_024451076.2:c.-32+954_… XM_024451076.2:c.-32+954_-32+965del	N/A	Intron Variant
PRELID3A transcript variant X4	XM_047437273.1:c.32+1166_… XM_047437273.1:c.32+1166_32+1177del	N/A	Intron Variant
PRELID3A transcript variant X1	XM_047437271.1:c.	N/A	Genic Upstream Transcript Variant
PRELID3A transcript variant X2	XM_047437272.1: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)₁₂	del(T)₁₁	del(T)₉	del(T)₈	del(T)₇	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)₁₆	ins(T)₂₉
GRCh38.p14 chr 18	NC_000018.10:g.12409160_12409184=	NC_000018.10:g.12409173_12409184del	NC_000018.10:g.12409174_12409184del	NC_000018.10:g.12409176_12409184del	NC_000018.10:g.12409177_12409184del	NC_000018.10:g.12409178_12409184del	NC_000018.10:g.12409180_12409184del	NC_000018.10:g.12409181_12409184del	NC_000018.10:g.12409182_12409184del	NC_000018.10:g.12409183_12409184del	NC_000018.10:g.12409184del	NC_000018.10:g.12409184dup	NC_000018.10:g.12409183_12409184dup	NC_000018.10:g.12409182_12409184dup	NC_000018.10:g.12409181_12409184dup	NC_000018.10:g.12409180_12409184dup	NC_000018.10:g.12409179_12409184dup	NC_000018.10:g.12409178_12409184dup	NC_000018.10:g.12409177_12409184dup	NC_000018.10:g.12409176_12409184dup	NC_000018.10:g.12409175_12409184dup	NC_000018.10:g.12409174_12409184dup	NC_000018.10:g.12409173_12409184dup	NC_000018.10:g.12409172_12409184dup	NC_000018.10:g.12409171_12409184dup	NC_000018.10:g.12409169_12409184dup	NC_000018.10:g.12409184_12409185insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 18	NC_000018.9:g.12409159_12409183=	NC_000018.9:g.12409172_12409183del	NC_000018.9:g.12409173_12409183del	NC_000018.9:g.12409175_12409183del	NC_000018.9:g.12409176_12409183del	NC_000018.9:g.12409177_12409183del	NC_000018.9:g.12409179_12409183del	NC_000018.9:g.12409180_12409183del	NC_000018.9:g.12409181_12409183del	NC_000018.9:g.12409182_12409183del	NC_000018.9:g.12409183del	NC_000018.9:g.12409183dup	NC_000018.9:g.12409182_12409183dup	NC_000018.9:g.12409181_12409183dup	NC_000018.9:g.12409180_12409183dup	NC_000018.9:g.12409179_12409183dup	NC_000018.9:g.12409178_12409183dup	NC_000018.9:g.12409177_12409183dup	NC_000018.9:g.12409176_12409183dup	NC_000018.9:g.12409175_12409183dup	NC_000018.9:g.12409174_12409183dup	NC_000018.9:g.12409173_12409183dup	NC_000018.9:g.12409172_12409183dup	NC_000018.9:g.12409171_12409183dup	NC_000018.9:g.12409170_12409183dup	NC_000018.9:g.12409168_12409183dup	NC_000018.9:g.12409183_12409184insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PRELID3A transcript variant 1	NM_001142405.1:c.32+1153=	NM_001142405.1:c.32+1166_32+1177del	NM_001142405.1:c.32+1167_32+1177del	NM_001142405.1:c.32+1169_32+1177del	NM_001142405.1:c.32+1170_32+1177del	NM_001142405.1:c.32+1171_32+1177del	NM_001142405.1:c.32+1173_32+1177del	NM_001142405.1:c.32+1174_32+1177del	NM_001142405.1:c.32+1175_32+1177del	NM_001142405.1:c.32+1176_32+1177del	NM_001142405.1:c.32+1177del	NM_001142405.1:c.32+1177dup	NM_001142405.1:c.32+1176_32+1177dup	NM_001142405.1:c.32+1175_32+1177dup	NM_001142405.1:c.32+1174_32+1177dup	NM_001142405.1:c.32+1173_32+1177dup	NM_001142405.1:c.32+1172_32+1177dup	NM_001142405.1:c.32+1171_32+1177dup	NM_001142405.1:c.32+1170_32+1177dup	NM_001142405.1:c.32+1169_32+1177dup	NM_001142405.1:c.32+1168_32+1177dup	NM_001142405.1:c.32+1167_32+1177dup	NM_001142405.1:c.32+1166_32+1177dup	NM_001142405.1:c.32+1165_32+1177dup	NM_001142405.1:c.32+1164_32+1177dup	NM_001142405.1:c.32+1162_32+1177dup	NM_001142405.1:c.32+1177_32+1178insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PRELID3A transcript variant 1	NM_001142405.2:c.32+1153=	NM_001142405.2:c.32+1166_32+1177del	NM_001142405.2:c.32+1167_32+1177del	NM_001142405.2:c.32+1169_32+1177del	NM_001142405.2:c.32+1170_32+1177del	NM_001142405.2:c.32+1171_32+1177del	NM_001142405.2:c.32+1173_32+1177del	NM_001142405.2:c.32+1174_32+1177del	NM_001142405.2:c.32+1175_32+1177del	NM_001142405.2:c.32+1176_32+1177del	NM_001142405.2:c.32+1177del	NM_001142405.2:c.32+1177dup	NM_001142405.2:c.32+1176_32+1177dup	NM_001142405.2:c.32+1175_32+1177dup	NM_001142405.2:c.32+1174_32+1177dup	NM_001142405.2:c.32+1173_32+1177dup	NM_001142405.2:c.32+1172_32+1177dup	NM_001142405.2:c.32+1171_32+1177dup	NM_001142405.2:c.32+1170_32+1177dup	NM_001142405.2:c.32+1169_32+1177dup	NM_001142405.2:c.32+1168_32+1177dup	NM_001142405.2:c.32+1167_32+1177dup	NM_001142405.2:c.32+1166_32+1177dup	NM_001142405.2:c.32+1165_32+1177dup	NM_001142405.2:c.32+1164_32+1177dup	NM_001142405.2:c.32+1162_32+1177dup	NM_001142405.2:c.32+1177_32+1178insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PRELID3A transcript variant 2	NM_006553.3:c.32+1153=	NM_006553.3:c.32+1166_32+1177del	NM_006553.3:c.32+1167_32+1177del	NM_006553.3:c.32+1169_32+1177del	NM_006553.3:c.32+1170_32+1177del	NM_006553.3:c.32+1171_32+1177del	NM_006553.3:c.32+1173_32+1177del	NM_006553.3:c.32+1174_32+1177del	NM_006553.3:c.32+1175_32+1177del	NM_006553.3:c.32+1176_32+1177del	NM_006553.3:c.32+1177del	NM_006553.3:c.32+1177dup	NM_006553.3:c.32+1176_32+1177dup	NM_006553.3:c.32+1175_32+1177dup	NM_006553.3:c.32+1174_32+1177dup	NM_006553.3:c.32+1173_32+1177dup	NM_006553.3:c.32+1172_32+1177dup	NM_006553.3:c.32+1171_32+1177dup	NM_006553.3:c.32+1170_32+1177dup	NM_006553.3:c.32+1169_32+1177dup	NM_006553.3:c.32+1168_32+1177dup	NM_006553.3:c.32+1167_32+1177dup	NM_006553.3:c.32+1166_32+1177dup	NM_006553.3:c.32+1165_32+1177dup	NM_006553.3:c.32+1164_32+1177dup	NM_006553.3:c.32+1162_32+1177dup	NM_006553.3:c.32+1177_32+1178insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PRELID3A transcript variant 2	NM_006553.4:c.32+1153=	NM_006553.4:c.32+1166_32+1177del	NM_006553.4:c.32+1167_32+1177del	NM_006553.4:c.32+1169_32+1177del	NM_006553.4:c.32+1170_32+1177del	NM_006553.4:c.32+1171_32+1177del	NM_006553.4:c.32+1173_32+1177del	NM_006553.4:c.32+1174_32+1177del	NM_006553.4:c.32+1175_32+1177del	NM_006553.4:c.32+1176_32+1177del	NM_006553.4:c.32+1177del	NM_006553.4:c.32+1177dup	NM_006553.4:c.32+1176_32+1177dup	NM_006553.4:c.32+1175_32+1177dup	NM_006553.4:c.32+1174_32+1177dup	NM_006553.4:c.32+1173_32+1177dup	NM_006553.4:c.32+1172_32+1177dup	NM_006553.4:c.32+1171_32+1177dup	NM_006553.4:c.32+1170_32+1177dup	NM_006553.4:c.32+1169_32+1177dup	NM_006553.4:c.32+1168_32+1177dup	NM_006553.4:c.32+1167_32+1177dup	NM_006553.4:c.32+1166_32+1177dup	NM_006553.4:c.32+1165_32+1177dup	NM_006553.4:c.32+1164_32+1177dup	NM_006553.4:c.32+1162_32+1177dup	NM_006553.4:c.32+1177_32+1178insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PRELID3A transcript variant X3	XM_024451075.1:c.44+406=	XM_024451075.1:c.44+419_44+430del	XM_024451075.1:c.44+420_44+430del	XM_024451075.1:c.44+422_44+430del	XM_024451075.1:c.44+423_44+430del	XM_024451075.1:c.44+424_44+430del	XM_024451075.1:c.44+426_44+430del	XM_024451075.1:c.44+427_44+430del	XM_024451075.1:c.44+428_44+430del	XM_024451075.1:c.44+429_44+430del	XM_024451075.1:c.44+430del	XM_024451075.1:c.44+430dup	XM_024451075.1:c.44+429_44+430dup	XM_024451075.1:c.44+428_44+430dup	XM_024451075.1:c.44+427_44+430dup	XM_024451075.1:c.44+426_44+430dup	XM_024451075.1:c.44+425_44+430dup	XM_024451075.1:c.44+424_44+430dup	XM_024451075.1:c.44+423_44+430dup	XM_024451075.1:c.44+422_44+430dup	XM_024451075.1:c.44+421_44+430dup	XM_024451075.1:c.44+420_44+430dup	XM_024451075.1:c.44+419_44+430dup	XM_024451075.1:c.44+418_44+430dup	XM_024451075.1:c.44+417_44+430dup	XM_024451075.1:c.44+415_44+430dup	XM_024451075.1:c.44+430_44+431insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PRELID3A transcript variant X5	XM_024451076.2:c.-32+941=	XM_024451076.2:c.-32+954_-32+965del	XM_024451076.2:c.-32+955_-32+965del	XM_024451076.2:c.-32+957_-32+965del	XM_024451076.2:c.-32+958_-32+965del	XM_024451076.2:c.-32+959_-32+965del	XM_024451076.2:c.-32+961_-32+965del	XM_024451076.2:c.-32+962_-32+965del	XM_024451076.2:c.-32+963_-32+965del	XM_024451076.2:c.-32+964_-32+965del	XM_024451076.2:c.-32+965del	XM_024451076.2:c.-32+965dup	XM_024451076.2:c.-32+964_-32+965dup	XM_024451076.2:c.-32+963_-32+965dup	XM_024451076.2:c.-32+962_-32+965dup	XM_024451076.2:c.-32+961_-32+965dup	XM_024451076.2:c.-32+960_-32+965dup	XM_024451076.2:c.-32+959_-32+965dup	XM_024451076.2:c.-32+958_-32+965dup	XM_024451076.2:c.-32+957_-32+965dup	XM_024451076.2:c.-32+956_-32+965dup	XM_024451076.2:c.-32+955_-32+965dup	XM_024451076.2:c.-32+954_-32+965dup	XM_024451076.2:c.-32+953_-32+965dup	XM_024451076.2:c.-32+952_-32+965dup	XM_024451076.2:c.-32+950_-32+965dup	XM_024451076.2:c.-32+965_-32+966insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PRELID3A transcript variant X4	XM_047437273.1:c.32+1153=	XM_047437273.1:c.32+1166_32+1177del	XM_047437273.1:c.32+1167_32+1177del	XM_047437273.1:c.32+1169_32+1177del	XM_047437273.1:c.32+1170_32+1177del	XM_047437273.1:c.32+1171_32+1177del	XM_047437273.1:c.32+1173_32+1177del	XM_047437273.1:c.32+1174_32+1177del	XM_047437273.1:c.32+1175_32+1177del	XM_047437273.1:c.32+1176_32+1177del	XM_047437273.1:c.32+1177del	XM_047437273.1:c.32+1177dup	XM_047437273.1:c.32+1176_32+1177dup	XM_047437273.1:c.32+1175_32+1177dup	XM_047437273.1:c.32+1174_32+1177dup	XM_047437273.1:c.32+1173_32+1177dup	XM_047437273.1:c.32+1172_32+1177dup	XM_047437273.1:c.32+1171_32+1177dup	XM_047437273.1:c.32+1170_32+1177dup	XM_047437273.1:c.32+1169_32+1177dup	XM_047437273.1:c.32+1168_32+1177dup	XM_047437273.1:c.32+1167_32+1177dup	XM_047437273.1:c.32+1166_32+1177dup	XM_047437273.1:c.32+1165_32+1177dup	XM_047437273.1:c.32+1164_32+1177dup	XM_047437273.1:c.32+1162_32+1177dup	XM_047437273.1:c.32+1177_32+1178insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

50 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80854753	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95705757	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss96363318	Feb 13, 2009 (130)
4	PJP	ss294930868	May 09, 2011 (134)
5	PJP	ss294930869	May 09, 2011 (137)
6	EVA_GENOME_DK	ss1575118815	Apr 01, 2015 (144)
7	SWEGEN	ss3016180896	Nov 08, 2017 (151)
8	SWEGEN	ss3016180897	Nov 08, 2017 (151)
9	SWEGEN	ss3016180898	Nov 08, 2017 (151)
10	SWEGEN	ss3016180899	Nov 08, 2017 (151)
11	PACBIO	ss3788317698	Jul 13, 2019 (153)
12	PACBIO	ss3793257444	Jul 13, 2019 (153)
13	PACBIO	ss3798143676	Jul 13, 2019 (153)
14	EVA	ss3835068829	Apr 27, 2020 (154)
15	GNOMAD	ss4318354913	Apr 26, 2021 (155)
16	GNOMAD	ss4318354914	Apr 26, 2021 (155)
17	GNOMAD	ss4318354915	Apr 26, 2021 (155)
18	GNOMAD	ss4318354916	Apr 26, 2021 (155)
19	GNOMAD	ss4318354917	Apr 26, 2021 (155)
20	GNOMAD	ss4318354918	Apr 26, 2021 (155)
21	GNOMAD	ss4318354919	Apr 26, 2021 (155)
22	GNOMAD	ss4318354920	Apr 26, 2021 (155)
23	GNOMAD	ss4318354921	Apr 26, 2021 (155)
24	GNOMAD	ss4318354922	Apr 26, 2021 (155)
25	GNOMAD	ss4318354923	Apr 26, 2021 (155)
26	GNOMAD	ss4318354925	Apr 26, 2021 (155)
27	GNOMAD	ss4318354926	Apr 26, 2021 (155)
28	GNOMAD	ss4318354927	Apr 26, 2021 (155)
29	GNOMAD	ss4318354928	Apr 26, 2021 (155)
30	GNOMAD	ss4318354929	Apr 26, 2021 (155)
31	GNOMAD	ss4318354930	Apr 26, 2021 (155)
32	GNOMAD	ss4318354931	Apr 26, 2021 (155)
33	GNOMAD	ss4318354932	Apr 26, 2021 (155)
34	GNOMAD	ss4318354933	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5224228363	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5224228364	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5224228365	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5224228367	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5224228368	Apr 26, 2021 (155)
40	HUGCELL_USP	ss5497419600	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5497419601	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5781015785	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5781015786	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5781015787	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5781015789	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5781015790	Oct 16, 2022 (156)
47	EVA	ss5827260957	Oct 16, 2022 (156)
48	EVA	ss5827260958	Oct 16, 2022 (156)
49	EVA	ss5827260959	Oct 16, 2022 (156)
50	EVA	ss5851971852	Oct 16, 2022 (156)
51	The Danish reference pan genome	NC_000018.9 - 12409159	Apr 27, 2020 (154)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518393363 (NC_000018.10:12409159::TTTTTT 118/63478) Row 518393364 (NC_000018.10:12409159::TTTTTTT 28/63480) Row 518393365 (NC_000018.10:12409159::TTTTTTTT 25/63480)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 82197670 (NC_000018.9:12409158::TT 6078/16124) Row 82197671 (NC_000018.9:12409158::T 2315/16124) Row 82197672 (NC_000018.9:12409158::TTT 1145/16124)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 82197670 (NC_000018.9:12409158::TT 6078/16124) Row 82197671 (NC_000018.9:12409158::T 2315/16124) Row 82197672 (NC_000018.9:12409158::TTT 1145/16124)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 82197670 (NC_000018.9:12409158::TT 6078/16124) Row 82197671 (NC_000018.9:12409158::T 2315/16124) Row 82197672 (NC_000018.9:12409158::TTT 1145/16124)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 82197670 (NC_000018.9:12409158::TT 6078/16124) Row 82197671 (NC_000018.9:12409158::T 2315/16124) Row 82197672 (NC_000018.9:12409158::TTT 1145/16124)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 82197670 (NC_000018.9:12409158::TT 6078/16124) Row 82197671 (NC_000018.9:12409158::T 2315/16124) Row 82197672 (NC_000018.9:12409158::TTT 1145/16124)...	-	Apr 26, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 114852889 (NC_000018.10:12409159::TT 11738/27762) Row 114852890 (NC_000018.10:12409159::TTT 1956/27762) Row 114852891 (NC_000018.10:12409159::T 4681/27762)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 114852889 (NC_000018.10:12409159::TT 11738/27762) Row 114852890 (NC_000018.10:12409159::TTT 1956/27762) Row 114852891 (NC_000018.10:12409159::T 4681/27762)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 114852889 (NC_000018.10:12409159::TT 11738/27762) Row 114852890 (NC_000018.10:12409159::TTT 1956/27762) Row 114852891 (NC_000018.10:12409159::T 4681/27762)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 114852889 (NC_000018.10:12409159::TT 11738/27762) Row 114852890 (NC_000018.10:12409159::TTT 1956/27762) Row 114852891 (NC_000018.10:12409159::T 4681/27762)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 114852889 (NC_000018.10:12409159::TT 11738/27762) Row 114852890 (NC_000018.10:12409159::TTT 1956/27762) Row 114852891 (NC_000018.10:12409159::T 4681/27762)...	-	Oct 16, 2022 (156)
82	ALFA	NC_000018.10 - 12409160	Apr 26, 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).

Associated ID	History Updated (Build)
rs146977460	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4318354933	NC_000018.10:12409159:TTTTTTTTTTTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4318354932	NC_000018.10:12409159:TTTTTTTTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4318354931	NC_000018.10:12409159:TTTTTTTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4318354930	NC_000018.10:12409159:TTTTTTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4318354929	NC_000018.10:12409159:TTTTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4318354928	NC_000018.10:12409159:TTTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354927	NC_000018.10:12409159:TTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354926	NC_000018.10:12409159:TT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354925, ss5497419601	NC_000018.10:12409159:T:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294930869	NC_000018.8:12399183::T	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3016180897, ss5224228364	NC_000018.9:12409158::T	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5497419600, ss5781015787	NC_000018.10:12409159::T	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss80854753	NT_010859.14:12399183::T	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3016180898, ss3788317698, ss3793257444, ss3798143676, ss3835068829, ss5224228363, ss5827260957	NC_000018.9:12409158::TT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5781015785	NC_000018.10:12409159::TT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss96363318	NT_010859.14:12399158::TT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294930868	NC_000018.8:12399159::TTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
585965, ss1575118815, ss3016180896, ss5224228365, ss5827260958	NC_000018.9:12409158::TTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5781015786	NC_000018.10:12409159::TTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95705757	NT_010859.14:12399183::TTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3016180899, ss5224228367, ss5827260959	NC_000018.9:12409158::TTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5781015789, ss5851971852	NC_000018.10:12409159::TTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5224228368	NC_000018.9:12409158::TTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5781015790	NC_000018.10:12409159::TTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354913	NC_000018.10:12409159::TTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354914	NC_000018.10:12409159::TTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354915	NC_000018.10:12409159::TTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4487615159	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354916	NC_000018.10:12409159::TTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354917	NC_000018.10:12409159::TTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354918	NC_000018.10:12409159::TTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354919	NC_000018.10:12409159::TTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354920	NC_000018.10:12409159::TTTTTTTTTTT… NC_000018.10:12409159::TTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354921	NC_000018.10:12409159::TTTTTTTTTTT… NC_000018.10:12409159::TTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354922	NC_000018.10:12409159::TTTTTTTTTTT… NC_000018.10:12409159::TTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4318354923	NC_000018.10:12409159::TTTTTTTTTTT… NC_000018.10:12409159::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3272877292	NC_000018.10:12409159:TTTTTTTTTTT:	NC_000018.10:12409159:TTTTTTTTTTTT… NC_000018.10:12409159:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

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

No publications for rs71371255

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71371255