Name: rs60757813
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.

rs60757813

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:7777054-7777077 (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)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / 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)₁₅ / dup(A)₁₉ / ins(A)₂₅ / ins(A)₃₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.2967 (1486/5008, 1000G)
del(A)₁₃=0.000 (0/804, ALFA)
del(A)₁₂=0.000 (0/804, ALFA) (+ 14 more)
del(A)₁₀=0.000 (0/804, ALFA)
del(A)₉=0.000 (0/804, ALFA)
del(A)₈=0.000 (0/804, ALFA)
del(A)₇=0.000 (0/804, ALFA)
del(A)₆=0.000 (0/804, ALFA)
del(A)₅=0.000 (0/804, ALFA)
del(A)₄=0.000 (0/804, ALFA)
delAAA=0.000 (0/804, ALFA)
delAA=0.000 (0/804, ALFA)
delA=0.000 (0/804, ALFA)
dupA=0.000 (0/804, ALFA)
dupAA=0.000 (0/804, ALFA)
dupAAA=0.000 (0/804, ALFA)
dup(A)₄=0.000 (0/804, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KIN : 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	804	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	496	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	240	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	228	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	20	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	16	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	28	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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=0.7033	del(A)₁₃=0.2967
1000Genomes	African	Sub	1322	(A)₂₄=0.7852	del(A)₁₃=0.2148
1000Genomes	East Asian	Sub	1008	(A)₂₄=0.4603	del(A)₁₃=0.5397
1000Genomes	Europe	Sub	1006	(A)₂₄=0.7674	del(A)₁₃=0.2326
1000Genomes	South Asian	Sub	978	(A)₂₄=0.721	del(A)₁₃=0.279
1000Genomes	American	Sub	694	(A)₂₄=0.782	del(A)₁₃=0.218
Allele Frequency Aggregator	Total	Global	804	(A)₂₄=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	European	Sub	496	(A)₂₄=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	African	Sub	240	(A)₂₄=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	28	(A)₂₄=1.00	del(A)₁₃=0.00, del(A)₁₂=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, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	20	(A)₂₄=1.00	del(A)₁₃=0.00, del(A)₁₂=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, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	16	(A)₂₄=1.00	del(A)₁₃=0.00, del(A)₁₂=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, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	(A)₂₄=1.0	del(A)₁₃=0.0, del(A)₁₂=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, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	Asian	Sub	0	(A)₂₄=0	del(A)₁₃=0, del(A)₁₂=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, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=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 10	NC_000010.11:g.7777064_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777065_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777066_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777068_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777069_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777070_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777071_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777072_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777073_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777074_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777075_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777076_7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777077del
GRCh38.p14 chr 10	NC_000010.11:g.7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777076_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777075_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777074_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777073_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777072_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777071_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777070_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777069_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777063_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777059_7777077dup
GRCh38.p14 chr 10	NC_000010.11:g.7777077_7777078insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 10	NC_000010.11:g.7777077_7777078insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.7819027_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819028_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819029_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819031_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819032_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819033_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819034_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819035_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819036_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819037_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819038_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819039_7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819040del
GRCh37.p13 chr 10	NC_000010.10:g.7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819039_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819038_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819037_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819036_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819035_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819034_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819033_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819032_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819026_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819022_7819040dup
GRCh37.p13 chr 10	NC_000010.10:g.7819040_7819041insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.7819040_7819041insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: KIN, Kin17 DNA and RNA binding protein (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KIN transcript variant 1	NM_012311.4:c.559-1268_55… NM_012311.4:c.559-1268_559-1255del	N/A	Intron Variant
KIN transcript variant 3	NR_045609.2:n.	N/A	Intron Variant
KIN transcript variant X1	XM_006717434.5:c.559-1268… XM_006717434.5:c.559-1268_559-1255del	N/A	Intron Variant
KIN transcript variant X3	XM_006717435.5:c.241-1268… XM_006717435.5:c.241-1268_241-1255del	N/A	Intron Variant
KIN transcript variant X2	XR_930485.3:n.	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)₁₄	del(A)₁₃	del(A)₁₂	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)₁₅	dup(A)₁₉	ins(A)₂₅	ins(A)₃₆
GRCh38.p14 chr 10	NC_000010.11:g.7777054_7777077=	NC_000010.11:g.7777064_7777077del	NC_000010.11:g.7777065_7777077del	NC_000010.11:g.7777066_7777077del	NC_000010.11:g.7777068_7777077del	NC_000010.11:g.7777069_7777077del	NC_000010.11:g.7777070_7777077del	NC_000010.11:g.7777071_7777077del	NC_000010.11:g.7777072_7777077del	NC_000010.11:g.7777073_7777077del	NC_000010.11:g.7777074_7777077del	NC_000010.11:g.7777075_7777077del	NC_000010.11:g.7777076_7777077del	NC_000010.11:g.7777077del	NC_000010.11:g.7777077dup	NC_000010.11:g.7777076_7777077dup	NC_000010.11:g.7777075_7777077dup	NC_000010.11:g.7777074_7777077dup	NC_000010.11:g.7777073_7777077dup	NC_000010.11:g.7777072_7777077dup	NC_000010.11:g.7777071_7777077dup	NC_000010.11:g.7777070_7777077dup	NC_000010.11:g.7777069_7777077dup	NC_000010.11:g.7777063_7777077dup	NC_000010.11:g.7777059_7777077dup	NC_000010.11:g.7777077_7777078insAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:g.7777077_7777078insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.7819017_7819040=	NC_000010.10:g.7819027_7819040del	NC_000010.10:g.7819028_7819040del	NC_000010.10:g.7819029_7819040del	NC_000010.10:g.7819031_7819040del	NC_000010.10:g.7819032_7819040del	NC_000010.10:g.7819033_7819040del	NC_000010.10:g.7819034_7819040del	NC_000010.10:g.7819035_7819040del	NC_000010.10:g.7819036_7819040del	NC_000010.10:g.7819037_7819040del	NC_000010.10:g.7819038_7819040del	NC_000010.10:g.7819039_7819040del	NC_000010.10:g.7819040del	NC_000010.10:g.7819040dup	NC_000010.10:g.7819039_7819040dup	NC_000010.10:g.7819038_7819040dup	NC_000010.10:g.7819037_7819040dup	NC_000010.10:g.7819036_7819040dup	NC_000010.10:g.7819035_7819040dup	NC_000010.10:g.7819034_7819040dup	NC_000010.10:g.7819033_7819040dup	NC_000010.10:g.7819032_7819040dup	NC_000010.10:g.7819026_7819040dup	NC_000010.10:g.7819022_7819040dup	NC_000010.10:g.7819040_7819041insAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.10:g.7819040_7819041insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
KIN transcript variant 1	NM_012311.3:c.559-1255=	NM_012311.3:c.559-1268_559-1255del	NM_012311.3:c.559-1267_559-1255del	NM_012311.3:c.559-1266_559-1255del	NM_012311.3:c.559-1264_559-1255del	NM_012311.3:c.559-1263_559-1255del	NM_012311.3:c.559-1262_559-1255del	NM_012311.3:c.559-1261_559-1255del	NM_012311.3:c.559-1260_559-1255del	NM_012311.3:c.559-1259_559-1255del	NM_012311.3:c.559-1258_559-1255del	NM_012311.3:c.559-1257_559-1255del	NM_012311.3:c.559-1256_559-1255del	NM_012311.3:c.559-1255del	NM_012311.3:c.559-1255dup	NM_012311.3:c.559-1256_559-1255dup	NM_012311.3:c.559-1257_559-1255dup	NM_012311.3:c.559-1258_559-1255dup	NM_012311.3:c.559-1259_559-1255dup	NM_012311.3:c.559-1260_559-1255dup	NM_012311.3:c.559-1261_559-1255dup	NM_012311.3:c.559-1262_559-1255dup	NM_012311.3:c.559-1263_559-1255dup	NM_012311.3:c.559-1269_559-1255dup	NM_012311.3:c.559-1273_559-1255dup	NM_012311.3:c.559-1255_559-1254insTTTTTTTTTTTTTTTTTTTTTTTTT	NM_012311.3:c.559-1255_559-1254insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
KIN transcript variant 1	NM_012311.4:c.559-1255=	NM_012311.4:c.559-1268_559-1255del	NM_012311.4:c.559-1267_559-1255del	NM_012311.4:c.559-1266_559-1255del	NM_012311.4:c.559-1264_559-1255del	NM_012311.4:c.559-1263_559-1255del	NM_012311.4:c.559-1262_559-1255del	NM_012311.4:c.559-1261_559-1255del	NM_012311.4:c.559-1260_559-1255del	NM_012311.4:c.559-1259_559-1255del	NM_012311.4:c.559-1258_559-1255del	NM_012311.4:c.559-1257_559-1255del	NM_012311.4:c.559-1256_559-1255del	NM_012311.4:c.559-1255del	NM_012311.4:c.559-1255dup	NM_012311.4:c.559-1256_559-1255dup	NM_012311.4:c.559-1257_559-1255dup	NM_012311.4:c.559-1258_559-1255dup	NM_012311.4:c.559-1259_559-1255dup	NM_012311.4:c.559-1260_559-1255dup	NM_012311.4:c.559-1261_559-1255dup	NM_012311.4:c.559-1262_559-1255dup	NM_012311.4:c.559-1263_559-1255dup	NM_012311.4:c.559-1269_559-1255dup	NM_012311.4:c.559-1273_559-1255dup	NM_012311.4:c.559-1255_559-1254insTTTTTTTTTTTTTTTTTTTTTTTTT	NM_012311.4:c.559-1255_559-1254insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
KIN transcript variant X1	XM_006717434.5:c.559-1255=	XM_006717434.5:c.559-1268_559-1255del	XM_006717434.5:c.559-1267_559-1255del	XM_006717434.5:c.559-1266_559-1255del	XM_006717434.5:c.559-1264_559-1255del	XM_006717434.5:c.559-1263_559-1255del	XM_006717434.5:c.559-1262_559-1255del	XM_006717434.5:c.559-1261_559-1255del	XM_006717434.5:c.559-1260_559-1255del	XM_006717434.5:c.559-1259_559-1255del	XM_006717434.5:c.559-1258_559-1255del	XM_006717434.5:c.559-1257_559-1255del	XM_006717434.5:c.559-1256_559-1255del	XM_006717434.5:c.559-1255del	XM_006717434.5:c.559-1255dup	XM_006717434.5:c.559-1256_559-1255dup	XM_006717434.5:c.559-1257_559-1255dup	XM_006717434.5:c.559-1258_559-1255dup	XM_006717434.5:c.559-1259_559-1255dup	XM_006717434.5:c.559-1260_559-1255dup	XM_006717434.5:c.559-1261_559-1255dup	XM_006717434.5:c.559-1262_559-1255dup	XM_006717434.5:c.559-1263_559-1255dup	XM_006717434.5:c.559-1269_559-1255dup	XM_006717434.5:c.559-1273_559-1255dup	XM_006717434.5:c.559-1255_559-1254insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_006717434.5:c.559-1255_559-1254insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
KIN transcript variant X3	XM_006717435.5:c.241-1255=	XM_006717435.5:c.241-1268_241-1255del	XM_006717435.5:c.241-1267_241-1255del	XM_006717435.5:c.241-1266_241-1255del	XM_006717435.5:c.241-1264_241-1255del	XM_006717435.5:c.241-1263_241-1255del	XM_006717435.5:c.241-1262_241-1255del	XM_006717435.5:c.241-1261_241-1255del	XM_006717435.5:c.241-1260_241-1255del	XM_006717435.5:c.241-1259_241-1255del	XM_006717435.5:c.241-1258_241-1255del	XM_006717435.5:c.241-1257_241-1255del	XM_006717435.5:c.241-1256_241-1255del	XM_006717435.5:c.241-1255del	XM_006717435.5:c.241-1255dup	XM_006717435.5:c.241-1256_241-1255dup	XM_006717435.5:c.241-1257_241-1255dup	XM_006717435.5:c.241-1258_241-1255dup	XM_006717435.5:c.241-1259_241-1255dup	XM_006717435.5:c.241-1260_241-1255dup	XM_006717435.5:c.241-1261_241-1255dup	XM_006717435.5:c.241-1262_241-1255dup	XM_006717435.5:c.241-1263_241-1255dup	XM_006717435.5:c.241-1269_241-1255dup	XM_006717435.5:c.241-1273_241-1255dup	XM_006717435.5:c.241-1255_241-1254insTTTTTTTTTTTTTTTTTTTTTTTTT	XM_006717435.5:c.241-1255_241-1254insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

67 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79758206	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95532116	Feb 02, 2009 (130)
3	HUMANGENOME_JCVI	ss97599746	Mar 15, 2016 (147)
4	GMI	ss288995214	May 04, 2012 (137)
5	PJP	ss294640775	May 09, 2011 (142)
6	1000GENOMES	ss1369086980	Aug 21, 2014 (142)
7	SWEGEN	ss3005897297	Nov 08, 2017 (151)
8	EVA_DECODE	ss3689233171	Jul 13, 2019 (153)
9	EVA_DECODE	ss3689233172	Jul 13, 2019 (153)
10	EVA_DECODE	ss3689233173	Jul 13, 2019 (153)
11	EVA_DECODE	ss3689233174	Jul 13, 2019 (153)
12	EVA_DECODE	ss3689233175	Jul 13, 2019 (153)
13	PACBIO	ss3786574381	Jul 13, 2019 (153)
14	PACBIO	ss3791767866	Jul 13, 2019 (153)
15	PACBIO	ss3796649663	Jul 13, 2019 (153)
16	PACBIO	ss3796649664	Jul 13, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3813078516	Jul 13, 2019 (153)
18	EVA	ss3831954678	Apr 26, 2020 (154)
19	GNOMAD	ss4212515763	Apr 26, 2021 (155)
20	GNOMAD	ss4212515764	Apr 26, 2021 (155)
21	GNOMAD	ss4212515765	Apr 26, 2021 (155)
22	GNOMAD	ss4212515766	Apr 26, 2021 (155)
23	GNOMAD	ss4212515767	Apr 26, 2021 (155)
24	GNOMAD	ss4212515768	Apr 26, 2021 (155)
25	GNOMAD	ss4212515769	Apr 26, 2021 (155)
26	GNOMAD	ss4212515770	Apr 26, 2021 (155)
27	GNOMAD	ss4212515771	Apr 26, 2021 (155)
28	GNOMAD	ss4212515772	Apr 26, 2021 (155)
29	GNOMAD	ss4212515773	Apr 26, 2021 (155)
30	GNOMAD	ss4212515774	Apr 26, 2021 (155)
31	GNOMAD	ss4212515775	Apr 26, 2021 (155)
32	GNOMAD	ss4212515776	Apr 26, 2021 (155)
33	GNOMAD	ss4212515777	Apr 26, 2021 (155)
34	GNOMAD	ss4212515778	Apr 26, 2021 (155)
35	GNOMAD	ss4212515779	Apr 26, 2021 (155)
36	GNOMAD	ss4212515780	Apr 26, 2021 (155)
37	GNOMAD	ss4212515781	Apr 26, 2021 (155)
38	GNOMAD	ss4212515782	Apr 26, 2021 (155)
39	GNOMAD	ss4212515783	Apr 26, 2021 (155)
40	GNOMAD	ss4212515784	Apr 26, 2021 (155)
41	GNOMAD	ss4212515785	Apr 26, 2021 (155)
42	GNOMAD	ss4212515786	Apr 26, 2021 (155)
43	GNOMAD	ss4212515787	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5196152616	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5196152617	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5196152618	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5196152619	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5196152620	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5196152621	Apr 26, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5282833638	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5282833639	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5282833640	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5282833641	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5282833642	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5282833643	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5478619828	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5478619829	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5478619830	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5478619831	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5478619832	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5478619833	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5740968481	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5740968482	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5740968483	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5740968484	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5740968485	Oct 16, 2022 (156)
67	EVA	ss5849426619	Oct 16, 2022 (156)
68	1000Genomes	NC_000010.10 - 7819017	Oct 12, 2018 (152)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342750799 (NC_000010.11:7777053::A 22630/73724) Row 342750800 (NC_000010.11:7777053::AA 2177/73600) Row 342750801 (NC_000010.11:7777053::AAA 82/73638)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 54121923 (NC_000010.10:7819016:AAAAAAAAAAAAA: 4273/16598) Row 54121924 (NC_000010.10:7819016:A: 4709/16598) Row 54121925 (NC_000010.10:7819016::A 1010/16598)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 54121923 (NC_000010.10:7819016:AAAAAAAAAAAAA: 4273/16598) Row 54121924 (NC_000010.10:7819016:A: 4709/16598) Row 54121925 (NC_000010.10:7819016::A 1010/16598)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 54121923 (NC_000010.10:7819016:AAAAAAAAAAAAA: 4273/16598) Row 54121924 (NC_000010.10:7819016:A: 4709/16598) Row 54121925 (NC_000010.10:7819016::A 1010/16598)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 54121923 (NC_000010.10:7819016:AAAAAAAAAAAAA: 4273/16598) Row 54121924 (NC_000010.10:7819016:A: 4709/16598) Row 54121925 (NC_000010.10:7819016::A 1010/16598)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 54121923 (NC_000010.10:7819016:AAAAAAAAAAAAA: 4273/16598) Row 54121924 (NC_000010.10:7819016:A: 4709/16598) Row 54121925 (NC_000010.10:7819016::A 1010/16598)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 54121923 (NC_000010.10:7819016:AAAAAAAAAAAAA: 4273/16598) Row 54121924 (NC_000010.10:7819016:A: 4709/16598) Row 54121925 (NC_000010.10:7819016::A 1010/16598)...	-	Apr 26, 2021 (155)
101	14KJPN Submission ignored due to conflicting rows: Row 74805585 (NC_000010.11:7777053:AAAAAAAAAAAAA: 7397/28208) Row 74805586 (NC_000010.11:7777053:AA: 171/28208) Row 74805587 (NC_000010.11:7777053:A: 10040/28208)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 74805585 (NC_000010.11:7777053:AAAAAAAAAAAAA: 7397/28208) Row 74805586 (NC_000010.11:7777053:AA: 171/28208) Row 74805587 (NC_000010.11:7777053:A: 10040/28208)...	-	Oct 16, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 74805585 (NC_000010.11:7777053:AAAAAAAAAAAAA: 7397/28208) Row 74805586 (NC_000010.11:7777053:AA: 171/28208) Row 74805587 (NC_000010.11:7777053:A: 10040/28208)...	-	Oct 16, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 74805585 (NC_000010.11:7777053:AAAAAAAAAAAAA: 7397/28208) Row 74805586 (NC_000010.11:7777053:AA: 171/28208) Row 74805587 (NC_000010.11:7777053:A: 10040/28208)...	-	Oct 16, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 74805585 (NC_000010.11:7777053:AAAAAAAAAAAAA: 7397/28208) Row 74805586 (NC_000010.11:7777053:AA: 171/28208) Row 74805587 (NC_000010.11:7777053:A: 10040/28208)...	-	Oct 16, 2022 (156)
106	ALFA	NC_000010.11 - 7777054	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)
rs139155830	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4212515787	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss288995214	NC_000010.9:7859022:AAAAAAAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
48521952, ss1369086980, ss3005897297, ss3786574381, ss3791767866, ss3796649663, ss5196152616	NC_000010.10:7819016:AAAAAAAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3813078516, ss4212515786, ss5282833643, ss5478619833, ss5740968481, ss5849426619	NC_000010.11:7777053:AAAAAAAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4212515785	NC_000010.11:7777053:AAAAAAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4212515784	NC_000010.11:7777053:AAAAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4212515783	NC_000010.11:7777053:AAAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4212515782	NC_000010.11:7777053:AAAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4212515781	NC_000010.11:7777053:AAAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3831954678	NC_000010.10:7819016:AAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4212515780	NC_000010.11:7777053:AAAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4212515779	NC_000010.11:7777053:AAAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4212515778	NC_000010.11:7777053:AAAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3689233175, ss4212515777, ss5282833642, ss5478619832	NC_000010.11:7777053:AAA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss79758206	NC_000010.8:7859044:AA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5196152619	NC_000010.10:7819016:AA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515776, ss5282833638, ss5478619831, ss5740968482	NC_000010.11:7777053:AA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3689233174	NC_000010.11:7777054:AA:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss294640775	NC_000010.9:7859045:A:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3796649664, ss5196152617	NC_000010.10:7819016:A:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5282833639, ss5478619830, ss5740968483	NC_000010.11:7777053:A:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3689233173	NC_000010.11:7777055:A:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95532116, ss97599746	NT_008705.16:7759039:A:	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5196152618	NC_000010.10:7819016::A	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515763, ss5282833640, ss5478619828, ss5740968484	NC_000010.11:7777053::A	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3689233172	NC_000010.11:7777056::A	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss97599746	NT_008705.16:7759039:A:AA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5196152621	NC_000010.10:7819016::AA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515764, ss5282833641, ss5478619829, ss5740968485	NC_000010.11:7777053::AA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3689233171	NC_000010.11:7777056::AA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515765	NC_000010.11:7777053::AAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515766	NC_000010.11:7777053::AAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12953764279	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5196152620	NC_000010.10:7819016::AAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515767	NC_000010.11:7777053::AAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515768	NC_000010.11:7777053::AAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515769	NC_000010.11:7777053::AAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515770	NC_000010.11:7777053::AAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515771	NC_000010.11:7777053::AAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515772	NC_000010.11:7777053::AAAAAAAAAAAA… NC_000010.11:7777053::AAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515773	NC_000010.11:7777053::AAAAAAAAAAAA… NC_000010.11:7777053::AAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515774	NC_000010.11:7777053::AAAAAAAAAAAA… NC_000010.11:7777053::AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4212515775	NC_000010.11:7777053::AAAAAAAAAAAA… NC_000010.11:7777053::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:7777053:AAAAAAAAAAAAA… NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs60757813

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

rs60757813