Name: rs10699634
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.

rs10699634

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:75524778-75524801 (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(A)₁₅ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₅ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₉ / dup(A)₂₄ / ins(A)₃₃ / ins(A)₃₄ / ins(A)₃₆
Variation Type: Indel Insertion and Deletion
Frequency: (A)₂₄=0.2382 (1193/5008, 1000G)
del(A)₁₅=0.00 (0/72, ALFA)
del(A)₁₃=0.00 (0/72, ALFA) (+ 16 more)
del(A)₁₂=0.00 (0/72, ALFA)
del(A)₁₁=0.00 (0/72, ALFA)
del(A)₁₀=0.00 (0/72, ALFA)
del(A)₉=0.00 (0/72, ALFA)
del(A)₈=0.00 (0/72, ALFA)
del(A)₇=0.00 (0/72, ALFA)
del(A)₆=0.00 (0/72, ALFA)
del(A)₅=0.00 (0/72, ALFA)
del(A)₄=0.00 (0/72, ALFA)
delAA=0.00 (0/72, ALFA)
delA=0.00 (0/72, ALFA)
dupA=0.00 (0/72, ALFA)
dupAA=0.00 (0/72, ALFA)
dupAAA=0.00 (0/72, ALFA)
dup(A)₄=0.00 (0/72, ALFA)
dup(A)₅=0.00 (0/72, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PTPN9 : 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	72	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
European	Sub	14	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	26	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	26	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	22	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₄=0.2382	del(A)₁₁=0.7618
1000Genomes	African	Sub	1322	(A)₂₄=0.4107	del(A)₁₁=0.5893
1000Genomes	East Asian	Sub	1008	(A)₂₄=0.1141	del(A)₁₁=0.8859
1000Genomes	Europe	Sub	1006	(A)₂₄=0.1213	del(A)₁₁=0.8787
1000Genomes	South Asian	Sub	978	(A)₂₄=0.191	del(A)₁₁=0.809
1000Genomes	American	Sub	694	(A)₂₄=0.326	del(A)₁₁=0.674
Allele Frequency Aggregator	Total	Global	72	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	African	Sub	26	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	22	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	European	Sub	14	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Other	Sub	4	(A)₂₄=1.0	del(A)₁₅=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₂₄=1.0	del(A)₁₅=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Latin American 1	Sub	2	(A)₂₄=1.0	del(A)₁₅=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₄=0	del(A)₁₅=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 15	NC_000015.10:g.75524787_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524789_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524790_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524791_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524792_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524793_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524794_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524795_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524796_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524797_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524798_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524799_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524800_75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524801del
GRCh38.p14 chr 15	NC_000015.10:g.75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524800_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524799_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524798_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524797_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524796_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524795_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524794_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524793_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524792_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524791_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524783_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524778_75524801dup
GRCh38.p14 chr 15	NC_000015.10:g.75524801_75524802insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.75524801_75524802insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.75524801_75524802insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.75817128_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817130_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817131_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817132_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817133_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817134_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817135_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817136_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817137_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817138_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817139_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817140_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817141_75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817142del
GRCh37.p13 chr 15	NC_000015.9:g.75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817141_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817140_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817139_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817138_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817137_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817136_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817135_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817134_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817133_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817132_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817124_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817119_75817142dup
GRCh37.p13 chr 15	NC_000015.9:g.75817142_75817143insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.75817142_75817143insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.75817142_75817143insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: PTPN9, protein tyrosine phosphatase non-receptor type 9 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PTPN9 transcript	NM_002833.4:c.208-494_208… NM_002833.4:c.208-494_208-480del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(A)₂₄=	del(A)₁₅	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₉	dup(A)₂₄	ins(A)₃₃	ins(A)₃₄	ins(A)₃₆
GRCh38.p14 chr 15	NC_000015.10:g.75524778_75524801=	NC_000015.10:g.75524787_75524801del	NC_000015.10:g.75524789_75524801del	NC_000015.10:g.75524790_75524801del	NC_000015.10:g.75524791_75524801del	NC_000015.10:g.75524792_75524801del	NC_000015.10:g.75524793_75524801del	NC_000015.10:g.75524794_75524801del	NC_000015.10:g.75524795_75524801del	NC_000015.10:g.75524796_75524801del	NC_000015.10:g.75524797_75524801del	NC_000015.10:g.75524798_75524801del	NC_000015.10:g.75524799_75524801del	NC_000015.10:g.75524800_75524801del	NC_000015.10:g.75524801del	NC_000015.10:g.75524801dup	NC_000015.10:g.75524800_75524801dup	NC_000015.10:g.75524799_75524801dup	NC_000015.10:g.75524798_75524801dup	NC_000015.10:g.75524797_75524801dup	NC_000015.10:g.75524796_75524801dup	NC_000015.10:g.75524795_75524801dup	NC_000015.10:g.75524794_75524801dup	NC_000015.10:g.75524793_75524801dup	NC_000015.10:g.75524792_75524801dup	NC_000015.10:g.75524791_75524801dup	NC_000015.10:g.75524783_75524801dup	NC_000015.10:g.75524778_75524801dup	NC_000015.10:g.75524801_75524802insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:g.75524801_75524802insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:g.75524801_75524802insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.75817119_75817142=	NC_000015.9:g.75817128_75817142del	NC_000015.9:g.75817130_75817142del	NC_000015.9:g.75817131_75817142del	NC_000015.9:g.75817132_75817142del	NC_000015.9:g.75817133_75817142del	NC_000015.9:g.75817134_75817142del	NC_000015.9:g.75817135_75817142del	NC_000015.9:g.75817136_75817142del	NC_000015.9:g.75817137_75817142del	NC_000015.9:g.75817138_75817142del	NC_000015.9:g.75817139_75817142del	NC_000015.9:g.75817140_75817142del	NC_000015.9:g.75817141_75817142del	NC_000015.9:g.75817142del	NC_000015.9:g.75817142dup	NC_000015.9:g.75817141_75817142dup	NC_000015.9:g.75817140_75817142dup	NC_000015.9:g.75817139_75817142dup	NC_000015.9:g.75817138_75817142dup	NC_000015.9:g.75817137_75817142dup	NC_000015.9:g.75817136_75817142dup	NC_000015.9:g.75817135_75817142dup	NC_000015.9:g.75817134_75817142dup	NC_000015.9:g.75817133_75817142dup	NC_000015.9:g.75817132_75817142dup	NC_000015.9:g.75817124_75817142dup	NC_000015.9:g.75817119_75817142dup	NC_000015.9:g.75817142_75817143insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.9:g.75817142_75817143insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.9:g.75817142_75817143insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
PTPN9 transcript	NM_002833.2:c.208-480=	NM_002833.2:c.208-494_208-480del	NM_002833.2:c.208-492_208-480del	NM_002833.2:c.208-491_208-480del	NM_002833.2:c.208-490_208-480del	NM_002833.2:c.208-489_208-480del	NM_002833.2:c.208-488_208-480del	NM_002833.2:c.208-487_208-480del	NM_002833.2:c.208-486_208-480del	NM_002833.2:c.208-485_208-480del	NM_002833.2:c.208-484_208-480del	NM_002833.2:c.208-483_208-480del	NM_002833.2:c.208-482_208-480del	NM_002833.2:c.208-481_208-480del	NM_002833.2:c.208-480del	NM_002833.2:c.208-480dup	NM_002833.2:c.208-481_208-480dup	NM_002833.2:c.208-482_208-480dup	NM_002833.2:c.208-483_208-480dup	NM_002833.2:c.208-484_208-480dup	NM_002833.2:c.208-485_208-480dup	NM_002833.2:c.208-486_208-480dup	NM_002833.2:c.208-487_208-480dup	NM_002833.2:c.208-488_208-480dup	NM_002833.2:c.208-489_208-480dup	NM_002833.2:c.208-490_208-480dup	NM_002833.2:c.208-498_208-480dup	NM_002833.2:c.208-503_208-480dup	NM_002833.2:c.208-480_208-479insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_002833.2:c.208-480_208-479insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_002833.2:c.208-480_208-479insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
PTPN9 transcript	NM_002833.4:c.208-480=	NM_002833.4:c.208-494_208-480del	NM_002833.4:c.208-492_208-480del	NM_002833.4:c.208-491_208-480del	NM_002833.4:c.208-490_208-480del	NM_002833.4:c.208-489_208-480del	NM_002833.4:c.208-488_208-480del	NM_002833.4:c.208-487_208-480del	NM_002833.4:c.208-486_208-480del	NM_002833.4:c.208-485_208-480del	NM_002833.4:c.208-484_208-480del	NM_002833.4:c.208-483_208-480del	NM_002833.4:c.208-482_208-480del	NM_002833.4:c.208-481_208-480del	NM_002833.4:c.208-480del	NM_002833.4:c.208-480dup	NM_002833.4:c.208-481_208-480dup	NM_002833.4:c.208-482_208-480dup	NM_002833.4:c.208-483_208-480dup	NM_002833.4:c.208-484_208-480dup	NM_002833.4:c.208-485_208-480dup	NM_002833.4:c.208-486_208-480dup	NM_002833.4:c.208-487_208-480dup	NM_002833.4:c.208-488_208-480dup	NM_002833.4:c.208-489_208-480dup	NM_002833.4:c.208-490_208-480dup	NM_002833.4:c.208-498_208-480dup	NM_002833.4:c.208-503_208-480dup	NM_002833.4:c.208-480_208-479insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_002833.4:c.208-480_208-479insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_002833.4:c.208-480_208-479insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

55 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81476564	Dec 14, 2007 (130)
2	HUMANGENOME_JCVI	ss95663805	Feb 06, 2009 (130)
3	GMI	ss289267199	May 04, 2012 (137)
4	SSMP	ss664286741	Apr 01, 2015 (144)
5	1000GENOMES	ss1375112364	Aug 21, 2014 (142)
6	SWEGEN	ss3013559596	Nov 08, 2017 (151)
7	URBANLAB	ss3650392898	Oct 12, 2018 (152)
8	EVA_DECODE	ss3698229156	Jul 13, 2019 (153)
9	EVA_DECODE	ss3698229157	Jul 13, 2019 (153)
10	EVA_DECODE	ss3698229158	Jul 13, 2019 (153)
11	EVA_DECODE	ss3698229159	Jul 13, 2019 (153)
12	EVA_DECODE	ss3698229160	Jul 13, 2019 (153)
13	KHV_HUMAN_GENOMES	ss3818605370	Jul 13, 2019 (153)
14	EVA	ss3834319456	Apr 27, 2020 (154)
15	GNOMAD	ss4291775723	Apr 27, 2021 (155)
16	GNOMAD	ss4291775724	Apr 27, 2021 (155)
17	GNOMAD	ss4291775725	Apr 27, 2021 (155)
18	GNOMAD	ss4291775726	Apr 27, 2021 (155)
19	GNOMAD	ss4291775727	Apr 27, 2021 (155)
20	GNOMAD	ss4291775728	Apr 27, 2021 (155)
21	GNOMAD	ss4291775729	Apr 27, 2021 (155)
22	GNOMAD	ss4291775730	Apr 27, 2021 (155)
23	GNOMAD	ss4291775731	Apr 27, 2021 (155)
24	GNOMAD	ss4291775732	Apr 27, 2021 (155)
25	GNOMAD	ss4291775733	Apr 27, 2021 (155)
26	GNOMAD	ss4291775734	Apr 27, 2021 (155)
27	GNOMAD	ss4291775735	Apr 27, 2021 (155)
28	GNOMAD	ss4291775736	Apr 27, 2021 (155)
29	GNOMAD	ss4291775737	Apr 27, 2021 (155)
30	GNOMAD	ss4291775738	Apr 27, 2021 (155)
31	GNOMAD	ss4291775740	Apr 27, 2021 (155)
32	GNOMAD	ss4291775741	Apr 27, 2021 (155)
33	GNOMAD	ss4291775742	Apr 27, 2021 (155)
34	GNOMAD	ss4291775743	Apr 27, 2021 (155)
35	GNOMAD	ss4291775744	Apr 27, 2021 (155)
36	GNOMAD	ss4291775745	Apr 27, 2021 (155)
37	GNOMAD	ss4291775746	Apr 27, 2021 (155)
38	GNOMAD	ss4291775747	Apr 27, 2021 (155)
39	GNOMAD	ss4291775748	Apr 27, 2021 (155)
40	GNOMAD	ss4291775749	Apr 27, 2021 (155)
41	GNOMAD	ss4291775750	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5216993608	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5216993609	Apr 27, 2021 (155)
44	TOMMO_GENOMICS	ss5216993610	Apr 27, 2021 (155)
45	TOMMO_GENOMICS	ss5216993611	Apr 27, 2021 (155)
46	TOMMO_GENOMICS	ss5216993612	Apr 27, 2021 (155)
47	HUGCELL_USP	ss5492707845	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5492707846	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5492707847	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5771039820	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5771039821	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5771039822	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5771039823	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5771039824	Oct 16, 2022 (156)
55	EVA	ss5851362960	Oct 16, 2022 (156)
56	1000Genomes	NC_000015.9 - 75817119	Oct 12, 2018 (152)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474089437 (NC_000015.10:75524777::A 42680/68062) Row 474089438 (NC_000015.10:75524777::AA 6645/68318) Row 474089439 (NC_000015.10:75524777::AAA 579/68322)...	-	Apr 27, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 74962915 (NC_000015.9:75817118::A 5348/14302) Row 74962916 (NC_000015.9:75817118:AAAAAAAA: 685/14302) Row 74962917 (NC_000015.9:75817118::AA 3244/14302)...	-	Apr 27, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 74962915 (NC_000015.9:75817118::A 5348/14302) Row 74962916 (NC_000015.9:75817118:AAAAAAAA: 685/14302) Row 74962917 (NC_000015.9:75817118::AA 3244/14302)...	-	Apr 27, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 74962915 (NC_000015.9:75817118::A 5348/14302) Row 74962916 (NC_000015.9:75817118:AAAAAAAA: 685/14302) Row 74962917 (NC_000015.9:75817118::AA 3244/14302)...	-	Apr 27, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 74962915 (NC_000015.9:75817118::A 5348/14302) Row 74962916 (NC_000015.9:75817118:AAAAAAAA: 685/14302) Row 74962917 (NC_000015.9:75817118::AA 3244/14302)...	-	Apr 27, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 74962915 (NC_000015.9:75817118::A 5348/14302) Row 74962916 (NC_000015.9:75817118:AAAAAAAA: 685/14302) Row 74962917 (NC_000015.9:75817118::AA 3244/14302)...	-	Apr 27, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 104876924 (NC_000015.10:75524777::A 10990/26420) Row 104876925 (NC_000015.10:75524777:AAAAAAAA: 1210/26420) Row 104876926 (NC_000015.10:75524777::AA 7052/26420)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 104876924 (NC_000015.10:75524777::A 10990/26420) Row 104876925 (NC_000015.10:75524777:AAAAAAAA: 1210/26420) Row 104876926 (NC_000015.10:75524777::AA 7052/26420)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 104876924 (NC_000015.10:75524777::A 10990/26420) Row 104876925 (NC_000015.10:75524777:AAAAAAAA: 1210/26420) Row 104876926 (NC_000015.10:75524777::AA 7052/26420)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 104876924 (NC_000015.10:75524777::A 10990/26420) Row 104876925 (NC_000015.10:75524777:AAAAAAAA: 1210/26420) Row 104876926 (NC_000015.10:75524777::AA 7052/26420)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 104876924 (NC_000015.10:75524777::A 10990/26420) Row 104876925 (NC_000015.10:75524777:AAAAAAAA: 1210/26420) Row 104876926 (NC_000015.10:75524777::AA 7052/26420)...	-	Oct 16, 2022 (156)
94	ALFA	NC_000015.10 - 75524778	Apr 27, 2021 (155)

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

Associated ID	History Updated (Build)
rs57699523	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4291775750	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4291775749	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3698229160, ss4291775748	NC_000015.10:75524777:AAAAAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
67243119, ss1375112364, ss3013559596	NC_000015.9:75817118:AAAAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3818605370, ss4291775747, ss5492707846	NC_000015.10:75524777:AAAAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3698229159	NC_000015.10:75524778:AAAAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4291775746	NC_000015.10:75524777:AAAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss289267199	NC_000015.8:73604173:AAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5216993609	NC_000015.9:75817118:AAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4291775745, ss5771039821	NC_000015.10:75524777:AAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4291775744	NC_000015.10:75524777:AAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4291775743	NC_000015.10:75524777:AAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4291775742	NC_000015.10:75524777:AAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775741	NC_000015.10:75524777:AA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775740, ss5492707847	NC_000015.10:75524777:A:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3698229158	NC_000015.10:75524788:A:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss664286741, ss3834319456, ss5216993608	NC_000015.9:75817118::A	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775723, ss5492707845, ss5771039820, ss5851362960	NC_000015.10:75524777::A	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3698229157	NC_000015.10:75524789::A	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95663805	NT_010194.17:46607699::A	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5216993610	NC_000015.9:75817118::AA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775724, ss5771039822	NC_000015.10:75524777::AA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3698229156	NC_000015.10:75524789::AA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3650392898	NC_000015.10:75524796::AA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss81476564	NT_010194.17:46607699::AA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5216993611	NC_000015.9:75817118::AAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775725, ss5771039823	NC_000015.10:75524777::AAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5216993612	NC_000015.9:75817118::AAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775726, ss5771039824	NC_000015.10:75524777::AAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775727	NC_000015.10:75524777::AAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10861287303	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775728	NC_000015.10:75524777::AAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775729	NC_000015.10:75524777::AAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775730	NC_000015.10:75524777::AAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775731	NC_000015.10:75524777::AAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775732	NC_000015.10:75524777::AAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775733	NC_000015.10:75524777::AAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775734	NC_000015.10:75524777::AAAAAAAAAAA… NC_000015.10:75524777::AAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775735	NC_000015.10:75524777::AAAAAAAAAAA… NC_000015.10:75524777::AAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775736	NC_000015.10:75524777::AAAAAAAAAAA… NC_000015.10:75524777::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775737	NC_000015.10:75524777::AAAAAAAAAAA… NC_000015.10:75524777::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4291775738	NC_000015.10:75524777::AAAAAAAAAAA… NC_000015.10:75524777::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3232148561	NC_000015.10:75524777:AAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
ss3232148565	NC_000015.10:75524777:AAAAAAAAA:	NC_000015.10:75524777:AAAAAAAAAAAA… NC_000015.10:75524777:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

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

No publications for rs10699634

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

rs10699634