Name: rs57634251
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.

rs57634251

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:112741941-112741967 (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)₁₇ / del(T)₁₅ / del(T)₁₄ / d…
del(T)₁₇ / del(T)₁₅ / del(T)₁₄ / 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)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.1129 (944/8364, ALFA)
(T)₂₇=0.4541 (2274/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NT5DC4 : Intron Variant
CKAP2L : 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	8364	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.8812	TTTTTTTTTT=0.0000, 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=0.0054, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1129, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.839545	0.06365	0.096805	32
European	Sub	7882	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.8740	TTTTTTTTTT=0.0000, 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=0.0057, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.1196, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.829864	0.067592	0.102544	32
African	Sub	318	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	302	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	20	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	38	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	82	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.99	TTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.97561	0.0	0.02439	0

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	8364	(T)₂₇=0.8812	del(T)₁₇=0.0000, del(T)₁₅=0.0000, del(T)₁₄=0.0000, 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=0.0054, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.1129, dupT=0.0006, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	7882	(T)₂₇=0.8740	del(T)₁₇=0.0000, del(T)₁₅=0.0000, del(T)₁₄=0.0000, 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=0.0057, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.1196, dupT=0.0006, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	318	(T)₂₇=1.000	del(T)₁₇=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, 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
Allele Frequency Aggregator	Other	Sub	82	(T)₂₇=0.99	del(T)₁₇=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, 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=0.01, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 2	Sub	38	(T)₂₇=1.00	del(T)₁₇=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, 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=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(T)₂₇=1.00	del(T)₁₇=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, 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=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(T)₂₇=1.00	del(T)₁₇=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, 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=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	6	(T)₂₇=1.0	del(T)₁₇=0.0, del(T)₁₅=0.0, del(T)₁₄=0.0, 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
1000Genomes	Global	Study-wide	5008	(T)₂₇=0.4541	delT=0.5459
1000Genomes	African	Sub	1322	(T)₂₇=0.4660	delT=0.5340
1000Genomes	East Asian	Sub	1008	(T)₂₇=0.3829	delT=0.6171
1000Genomes	Europe	Sub	1006	(T)₂₇=0.3847	delT=0.6153
1000Genomes	South Asian	Sub	978	(T)₂₇=0.548	delT=0.452
1000Genomes	American	Sub	694	(T)₂₇=0.503	delT=0.497

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 2	NC_000002.12:g.112741951_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741953_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741954_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741955_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741956_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741957_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741958_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741959_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741960_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741961_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741962_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741963_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741964_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741965_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741966_112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741967del
GRCh38.p14 chr 2	NC_000002.12:g.112741967dup
GRCh38.p14 chr 2	NC_000002.12:g.112741966_112741967dup
GRCh38.p14 chr 2	NC_000002.12:g.112741965_112741967dup
GRCh38.p14 chr 2	NC_000002.12:g.112741964_112741967dup
GRCh38.p14 chr 2	NC_000002.12:g.112741955_112741967dup
GRCh37.p13 chr 2	NC_000002.11:g.113499528_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499530_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499531_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499532_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499533_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499534_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499535_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499536_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499537_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499538_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499539_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499540_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499541_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499542_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499543_113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499544del
GRCh37.p13 chr 2	NC_000002.11:g.113499544dup
GRCh37.p13 chr 2	NC_000002.11:g.113499543_113499544dup
GRCh37.p13 chr 2	NC_000002.11:g.113499542_113499544dup
GRCh37.p13 chr 2	NC_000002.11:g.113499541_113499544dup
GRCh37.p13 chr 2	NC_000002.11:g.113499532_113499544dup
CKAP2L RefSeqGene	NG_041820.1:g.27721_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27723_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27724_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27725_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27726_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27727_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27728_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27729_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27730_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27731_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27732_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27733_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27734_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27735_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27736_27737del
CKAP2L RefSeqGene	NG_041820.1:g.27737del
CKAP2L RefSeqGene	NG_041820.1:g.27737dup
CKAP2L RefSeqGene	NG_041820.1:g.27736_27737dup
CKAP2L RefSeqGene	NG_041820.1:g.27735_27737dup
CKAP2L RefSeqGene	NG_041820.1:g.27734_27737dup
CKAP2L RefSeqGene	NG_041820.1:g.27725_27737dup

Gene: CKAP2L, cytoskeleton associated protein 2 like (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CKAP2L transcript variant 2	NM_001304361.2:c.1327+749… NM_001304361.2:c.1327+749_1327+765del	N/A	Intron Variant
CKAP2L transcript variant 1	NM_152515.5:c.1822+749_18… NM_152515.5:c.1822+749_1822+765del	N/A	Intron Variant
CKAP2L transcript variant 3	NR_130712.2:n.	N/A	Intron Variant
CKAP2L transcript variant X1	XM_011510666.3:c.1327+749… XM_011510666.3:c.1327+749_1327+765del	N/A	Intron Variant

Gene: NT5DC4, 5'-nucleotidase domain containing 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NT5DC4 transcript variant 2	NM_001350494.2:c.1249-461… NM_001350494.2:c.1249-461_1249-445del	N/A	Intron Variant
NT5DC4 transcript variant 1	NM_001393655.1:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X14	XM_017005475.1:c.1519-461… XM_017005475.1:c.1519-461_1519-445del	N/A	Intron Variant
NT5DC4 transcript variant X10	XM_024452802.2:c.1552-461… XM_024452802.2:c.1552-461_1552-445del	N/A	Intron Variant
NT5DC4 transcript variant X2	XM_011512262.3:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X24	XM_011512265.3:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X4	XM_017005474.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X17	XM_017005476.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X18	XM_017005477.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X20	XM_017005478.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X1	XM_024452799.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X3	XM_024452800.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X11	XM_024452803.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X12	XM_024452804.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X13	XM_024452805.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X15	XM_024452806.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X16	XM_024452807.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X19	XM_024452808.2:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X26	XM_024452809.1:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X28	XM_024452810.1:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X21	XM_047443973.1:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X30	XM_047443974.1:c.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X7	XR_002959269.2:n.	N/A	Intron Variant
NT5DC4 transcript variant X9	XR_001739644.2:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X5	XR_002959267.2:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X6	XR_002959268.2:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X8	XR_002959270.1:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X22	XR_002959272.1:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X23	XR_002959273.1:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X25	XR_002959274.1:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X27	XR_002959275.1:n.	N/A	Genic Downstream Transcript Variant
NT5DC4 transcript variant X29	XR_002959276.1:n.	N/A	Genic Downstream 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)₂₇=	del(T)₁₇	del(T)₁₅	del(T)₁₄	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)₁₃
GRCh38.p14 chr 2	NC_000002.12:g.112741941_112741967=	NC_000002.12:g.112741951_112741967del	NC_000002.12:g.112741953_112741967del	NC_000002.12:g.112741954_112741967del	NC_000002.12:g.112741955_112741967del	NC_000002.12:g.112741956_112741967del	NC_000002.12:g.112741957_112741967del	NC_000002.12:g.112741958_112741967del	NC_000002.12:g.112741959_112741967del	NC_000002.12:g.112741960_112741967del	NC_000002.12:g.112741961_112741967del	NC_000002.12:g.112741962_112741967del	NC_000002.12:g.112741963_112741967del	NC_000002.12:g.112741964_112741967del	NC_000002.12:g.112741965_112741967del	NC_000002.12:g.112741966_112741967del	NC_000002.12:g.112741967del	NC_000002.12:g.112741967dup	NC_000002.12:g.112741966_112741967dup	NC_000002.12:g.112741965_112741967dup	NC_000002.12:g.112741964_112741967dup	NC_000002.12:g.112741955_112741967dup
GRCh37.p13 chr 2	NC_000002.11:g.113499518_113499544=	NC_000002.11:g.113499528_113499544del	NC_000002.11:g.113499530_113499544del	NC_000002.11:g.113499531_113499544del	NC_000002.11:g.113499532_113499544del	NC_000002.11:g.113499533_113499544del	NC_000002.11:g.113499534_113499544del	NC_000002.11:g.113499535_113499544del	NC_000002.11:g.113499536_113499544del	NC_000002.11:g.113499537_113499544del	NC_000002.11:g.113499538_113499544del	NC_000002.11:g.113499539_113499544del	NC_000002.11:g.113499540_113499544del	NC_000002.11:g.113499541_113499544del	NC_000002.11:g.113499542_113499544del	NC_000002.11:g.113499543_113499544del	NC_000002.11:g.113499544del	NC_000002.11:g.113499544dup	NC_000002.11:g.113499543_113499544dup	NC_000002.11:g.113499542_113499544dup	NC_000002.11:g.113499541_113499544dup	NC_000002.11:g.113499532_113499544dup
CKAP2L RefSeqGene	NG_041820.1:g.27711_27737=	NG_041820.1:g.27721_27737del	NG_041820.1:g.27723_27737del	NG_041820.1:g.27724_27737del	NG_041820.1:g.27725_27737del	NG_041820.1:g.27726_27737del	NG_041820.1:g.27727_27737del	NG_041820.1:g.27728_27737del	NG_041820.1:g.27729_27737del	NG_041820.1:g.27730_27737del	NG_041820.1:g.27731_27737del	NG_041820.1:g.27732_27737del	NG_041820.1:g.27733_27737del	NG_041820.1:g.27734_27737del	NG_041820.1:g.27735_27737del	NG_041820.1:g.27736_27737del	NG_041820.1:g.27737del	NG_041820.1:g.27737dup	NG_041820.1:g.27736_27737dup	NG_041820.1:g.27735_27737dup	NG_041820.1:g.27734_27737dup	NG_041820.1:g.27725_27737dup
CKAP2L transcript variant 2	NM_001304361.2:c.1327+765=	NM_001304361.2:c.1327+749_1327+765del	NM_001304361.2:c.1327+751_1327+765del	NM_001304361.2:c.1327+752_1327+765del	NM_001304361.2:c.1327+753_1327+765del	NM_001304361.2:c.1327+754_1327+765del	NM_001304361.2:c.1327+755_1327+765del	NM_001304361.2:c.1327+756_1327+765del	NM_001304361.2:c.1327+757_1327+765del	NM_001304361.2:c.1327+758_1327+765del	NM_001304361.2:c.1327+759_1327+765del	NM_001304361.2:c.1327+760_1327+765del	NM_001304361.2:c.1327+761_1327+765del	NM_001304361.2:c.1327+762_1327+765del	NM_001304361.2:c.1327+763_1327+765del	NM_001304361.2:c.1327+764_1327+765del	NM_001304361.2:c.1327+765del	NM_001304361.2:c.1327+765dup	NM_001304361.2:c.1327+764_1327+765dup	NM_001304361.2:c.1327+763_1327+765dup	NM_001304361.2:c.1327+762_1327+765dup	NM_001304361.2:c.1327+753_1327+765dup
NT5DC4 transcript variant 2	NM_001350494.2:c.1249-471=	NM_001350494.2:c.1249-461_1249-445del	NM_001350494.2:c.1249-459_1249-445del	NM_001350494.2:c.1249-458_1249-445del	NM_001350494.2:c.1249-457_1249-445del	NM_001350494.2:c.1249-456_1249-445del	NM_001350494.2:c.1249-455_1249-445del	NM_001350494.2:c.1249-454_1249-445del	NM_001350494.2:c.1249-453_1249-445del	NM_001350494.2:c.1249-452_1249-445del	NM_001350494.2:c.1249-451_1249-445del	NM_001350494.2:c.1249-450_1249-445del	NM_001350494.2:c.1249-449_1249-445del	NM_001350494.2:c.1249-448_1249-445del	NM_001350494.2:c.1249-447_1249-445del	NM_001350494.2:c.1249-446_1249-445del	NM_001350494.2:c.1249-445del	NM_001350494.2:c.1249-445dup	NM_001350494.2:c.1249-446_1249-445dup	NM_001350494.2:c.1249-447_1249-445dup	NM_001350494.2:c.1249-448_1249-445dup	NM_001350494.2:c.1249-457_1249-445dup
CKAP2L transcript	NM_152515.3:c.1822+765=	NM_152515.3:c.1822+749_1822+765del	NM_152515.3:c.1822+751_1822+765del	NM_152515.3:c.1822+752_1822+765del	NM_152515.3:c.1822+753_1822+765del	NM_152515.3:c.1822+754_1822+765del	NM_152515.3:c.1822+755_1822+765del	NM_152515.3:c.1822+756_1822+765del	NM_152515.3:c.1822+757_1822+765del	NM_152515.3:c.1822+758_1822+765del	NM_152515.3:c.1822+759_1822+765del	NM_152515.3:c.1822+760_1822+765del	NM_152515.3:c.1822+761_1822+765del	NM_152515.3:c.1822+762_1822+765del	NM_152515.3:c.1822+763_1822+765del	NM_152515.3:c.1822+764_1822+765del	NM_152515.3:c.1822+765del	NM_152515.3:c.1822+765dup	NM_152515.3:c.1822+764_1822+765dup	NM_152515.3:c.1822+763_1822+765dup	NM_152515.3:c.1822+762_1822+765dup	NM_152515.3:c.1822+753_1822+765dup
CKAP2L transcript variant 1	NM_152515.5:c.1822+765=	NM_152515.5:c.1822+749_1822+765del	NM_152515.5:c.1822+751_1822+765del	NM_152515.5:c.1822+752_1822+765del	NM_152515.5:c.1822+753_1822+765del	NM_152515.5:c.1822+754_1822+765del	NM_152515.5:c.1822+755_1822+765del	NM_152515.5:c.1822+756_1822+765del	NM_152515.5:c.1822+757_1822+765del	NM_152515.5:c.1822+758_1822+765del	NM_152515.5:c.1822+759_1822+765del	NM_152515.5:c.1822+760_1822+765del	NM_152515.5:c.1822+761_1822+765del	NM_152515.5:c.1822+762_1822+765del	NM_152515.5:c.1822+763_1822+765del	NM_152515.5:c.1822+764_1822+765del	NM_152515.5:c.1822+765del	NM_152515.5:c.1822+765dup	NM_152515.5:c.1822+764_1822+765dup	NM_152515.5:c.1822+763_1822+765dup	NM_152515.5:c.1822+762_1822+765dup	NM_152515.5:c.1822+753_1822+765dup
CKAP2L transcript variant X1	XM_011510666.3:c.1327+765=	XM_011510666.3:c.1327+749_1327+765del	XM_011510666.3:c.1327+751_1327+765del	XM_011510666.3:c.1327+752_1327+765del	XM_011510666.3:c.1327+753_1327+765del	XM_011510666.3:c.1327+754_1327+765del	XM_011510666.3:c.1327+755_1327+765del	XM_011510666.3:c.1327+756_1327+765del	XM_011510666.3:c.1327+757_1327+765del	XM_011510666.3:c.1327+758_1327+765del	XM_011510666.3:c.1327+759_1327+765del	XM_011510666.3:c.1327+760_1327+765del	XM_011510666.3:c.1327+761_1327+765del	XM_011510666.3:c.1327+762_1327+765del	XM_011510666.3:c.1327+763_1327+765del	XM_011510666.3:c.1327+764_1327+765del	XM_011510666.3:c.1327+765del	XM_011510666.3:c.1327+765dup	XM_011510666.3:c.1327+764_1327+765dup	XM_011510666.3:c.1327+763_1327+765dup	XM_011510666.3:c.1327+762_1327+765dup	XM_011510666.3:c.1327+753_1327+765dup
NT5DC4 transcript variant X14	XM_017005475.1:c.1519-471=	XM_017005475.1:c.1519-461_1519-445del	XM_017005475.1:c.1519-459_1519-445del	XM_017005475.1:c.1519-458_1519-445del	XM_017005475.1:c.1519-457_1519-445del	XM_017005475.1:c.1519-456_1519-445del	XM_017005475.1:c.1519-455_1519-445del	XM_017005475.1:c.1519-454_1519-445del	XM_017005475.1:c.1519-453_1519-445del	XM_017005475.1:c.1519-452_1519-445del	XM_017005475.1:c.1519-451_1519-445del	XM_017005475.1:c.1519-450_1519-445del	XM_017005475.1:c.1519-449_1519-445del	XM_017005475.1:c.1519-448_1519-445del	XM_017005475.1:c.1519-447_1519-445del	XM_017005475.1:c.1519-446_1519-445del	XM_017005475.1:c.1519-445del	XM_017005475.1:c.1519-445dup	XM_017005475.1:c.1519-446_1519-445dup	XM_017005475.1:c.1519-447_1519-445dup	XM_017005475.1:c.1519-448_1519-445dup	XM_017005475.1:c.1519-457_1519-445dup
NT5DC4 transcript variant X10	XM_024452802.2:c.1552-471=	XM_024452802.2:c.1552-461_1552-445del	XM_024452802.2:c.1552-459_1552-445del	XM_024452802.2:c.1552-458_1552-445del	XM_024452802.2:c.1552-457_1552-445del	XM_024452802.2:c.1552-456_1552-445del	XM_024452802.2:c.1552-455_1552-445del	XM_024452802.2:c.1552-454_1552-445del	XM_024452802.2:c.1552-453_1552-445del	XM_024452802.2:c.1552-452_1552-445del	XM_024452802.2:c.1552-451_1552-445del	XM_024452802.2:c.1552-450_1552-445del	XM_024452802.2:c.1552-449_1552-445del	XM_024452802.2:c.1552-448_1552-445del	XM_024452802.2:c.1552-447_1552-445del	XM_024452802.2:c.1552-446_1552-445del	XM_024452802.2:c.1552-445del	XM_024452802.2:c.1552-445dup	XM_024452802.2:c.1552-446_1552-445dup	XM_024452802.2:c.1552-447_1552-445dup	XM_024452802.2:c.1552-448_1552-445dup	XM_024452802.2:c.1552-457_1552-445dup

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#.

54 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79966869	Aug 21, 2014 (142)
2	HGSV	ss80213433	Aug 21, 2014 (142)
3	HGSV	ss80228410	Aug 21, 2014 (142)
4	HUMANGENOME_JCVI	ss95281638	Feb 06, 2009 (138)
5	PJP	ss294997849	May 09, 2011 (144)
6	PJP	ss294997850	May 09, 2011 (144)
7	1000GENOMES	ss1368621640	Aug 21, 2014 (144)
8	SWEGEN	ss2990196934	Nov 08, 2017 (151)
9	URBANLAB	ss3647113876	Oct 11, 2018 (152)
10	PACBIO	ss3789528810	Jul 13, 2019 (153)
11	PACBIO	ss3794401607	Jul 13, 2019 (153)
12	KHV_HUMAN_GENOMES	ss3801587646	Jul 13, 2019 (153)
13	GNOMAD	ss4048478333	Apr 26, 2021 (155)
14	GNOMAD	ss4048478334	Apr 26, 2021 (155)
15	GNOMAD	ss4048478335	Apr 26, 2021 (155)
16	GNOMAD	ss4048478337	Apr 26, 2021 (155)
17	GNOMAD	ss4048478338	Apr 26, 2021 (155)
18	GNOMAD	ss4048478339	Apr 26, 2021 (155)
19	GNOMAD	ss4048478340	Apr 26, 2021 (155)
20	GNOMAD	ss4048478341	Apr 26, 2021 (155)
21	GNOMAD	ss4048478342	Apr 26, 2021 (155)
22	GNOMAD	ss4048478343	Apr 26, 2021 (155)
23	GNOMAD	ss4048478344	Apr 26, 2021 (155)
24	GNOMAD	ss4048478345	Apr 26, 2021 (155)
25	GNOMAD	ss4048478346	Apr 26, 2021 (155)
26	GNOMAD	ss4048478347	Apr 26, 2021 (155)
27	GNOMAD	ss4048478348	Apr 26, 2021 (155)
28	GNOMAD	ss4048478349	Apr 26, 2021 (155)
29	GNOMAD	ss4048478350	Apr 26, 2021 (155)
30	GNOMAD	ss4048478351	Apr 26, 2021 (155)
31	GNOMAD	ss4048478352	Apr 26, 2021 (155)
32	GNOMAD	ss4048478353	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5153253152	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5153253153	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5153253154	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5153253155	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5153253156	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5153253157	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5249537071	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5249537072	Oct 12, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5249537073	Oct 12, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5249537074	Oct 12, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5249537075	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5449429671	Oct 12, 2022 (156)
45	HUGCELL_USP	ss5449429672	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5449429673	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5449429674	Oct 12, 2022 (156)
48	SANFORD_IMAGENETICS	ss5629528626	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5683196202	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5683196203	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5683196204	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5683196205	Oct 12, 2022 (156)
53	EVA	ss5820620183	Oct 12, 2022 (156)
54	EVA	ss5820620184	Oct 12, 2022 (156)
55	1000Genomes	NC_000002.11 - 113499518	Oct 11, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 69935650 (NC_000002.12:112741940::T 1051/66834) Row 69935651 (NC_000002.12:112741940::TT 64/66822) Row 69935652 (NC_000002.12:112741940::TTT 10/66820)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 11222459 (NC_000002.11:113499517:T: 6804/15320) Row 11222460 (NC_000002.11:113499517::T 51/15320) Row 11222461 (NC_000002.11:113499517:TT: 23/15320)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 11222459 (NC_000002.11:113499517:T: 6804/15320) Row 11222460 (NC_000002.11:113499517::T 51/15320) Row 11222461 (NC_000002.11:113499517:TT: 23/15320)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 11222459 (NC_000002.11:113499517:T: 6804/15320) Row 11222460 (NC_000002.11:113499517::T 51/15320) Row 11222461 (NC_000002.11:113499517:TT: 23/15320)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 11222459 (NC_000002.11:113499517:T: 6804/15320) Row 11222460 (NC_000002.11:113499517::T 51/15320) Row 11222461 (NC_000002.11:113499517:TT: 23/15320)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 11222459 (NC_000002.11:113499517:T: 6804/15320) Row 11222460 (NC_000002.11:113499517::T 51/15320) Row 11222461 (NC_000002.11:113499517:TT: 23/15320)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 11222459 (NC_000002.11:113499517:T: 6804/15320) Row 11222460 (NC_000002.11:113499517::T 51/15320) Row 11222461 (NC_000002.11:113499517:TT: 23/15320)...	-	Apr 26, 2021 (155)
82	14KJPN Submission ignored due to conflicting rows: Row 17033306 (NC_000002.12:112741940:T: 14192/26066) Row 17033307 (NC_000002.12:112741940:TT: 29/26066) Row 17033308 (NC_000002.12:112741940::T 117/26066)...	-	Oct 12, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 17033306 (NC_000002.12:112741940:T: 14192/26066) Row 17033307 (NC_000002.12:112741940:TT: 29/26066) Row 17033308 (NC_000002.12:112741940::T 117/26066)...	-	Oct 12, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 17033306 (NC_000002.12:112741940:T: 14192/26066) Row 17033307 (NC_000002.12:112741940:TT: 29/26066) Row 17033308 (NC_000002.12:112741940::T 117/26066)...	-	Oct 12, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 17033306 (NC_000002.12:112741940:T: 14192/26066) Row 17033307 (NC_000002.12:112741940:TT: 29/26066) Row 17033308 (NC_000002.12:112741940::T 117/26066)...	-	Oct 12, 2022 (156)
86	ALFA	NC_000002.12 - 112741941	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)
rs61601764	Apr 25, 2013 (138)
rs72418224	Jul 01, 2015 (144)
rs139541122	May 11, 2012 (137)
rs145158319	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4048478353	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4048478352	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5153253155	NC_000002.11:113499517:TTTTTTTTTTT… NC_000002.11:113499517:TTTTTTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4048478351, ss5683196205	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4048478350	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4048478349	NC_000002.12:112741940:TTTTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4048478348	NC_000002.12:112741940:TTTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4048478347	NC_000002.12:112741940:TTTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5153253157	NC_000002.11:113499517:TTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4048478346	NC_000002.12:112741940:TTTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4048478345	NC_000002.12:112741940:TTTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss2990196934, ss5629528626	NC_000002.11:113499517:TTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478344, ss5249537075, ss5449429671	NC_000002.12:112741940:TTTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478343	NC_000002.12:112741940:TTTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5153253156	NC_000002.11:113499517:TTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478342, ss5249537072	NC_000002.12:112741940:TTTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss80213433	NC_000002.9:113215772:TTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478341, ss5249537073	NC_000002.12:112741940:TTT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss79966869, ss80228410	NC_000002.9:113215773:TT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5153253154, ss5820620183	NC_000002.11:113499517:TT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478340, ss5249537071, ss5449429673, ss5683196203	NC_000002.12:112741940:TT:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294997849	NC_000002.10:113215988:T:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294997850	NC_000002.10:113216014:T:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9790983, ss1368621640, ss3789528810, ss3794401607, ss5153253152	NC_000002.11:113499517:T:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3647113876, ss3801587646, ss4048478339, ss5449429672, ss5683196202	NC_000002.12:112741940:T:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95281638	NT_022135.16:3248206:T:	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5153253153	NC_000002.11:113499517::T	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478333, ss5249537074, ss5449429674, ss5683196204	NC_000002.12:112741940::T	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478334	NC_000002.12:112741940::TT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5820620184	NC_000002.11:113499517::TTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss4048478335	NC_000002.12:112741940::TTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10389597086	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478337	NC_000002.12:112741940::TTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048478338	NC_000002.12:112741940::TTTTTTTTTT… NC_000002.12:112741940::TTTTTTTTTTTTT	NC_000002.12:112741940:TTTTTTTTTTT… NC_000002.12:112741940:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs57634251

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

rs57634251