Name: rs36116401
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.

rs36116401

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:26369710-26369729 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₅ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₅ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₅=0.000 (0/180, ALFA)
del(T)₁₂=0.000 (0/180, ALFA)
del(T)₁₁=0.000 (0/180, ALFA) (+ 12 more)
del(T)₁₀=0.000 (0/180, ALFA)
del(T)₉=0.000 (0/180, ALFA)
del(T)₈=0.000 (0/180, ALFA)
del(T)₇=0.000 (0/180, ALFA)
del(T)₆=0.000 (0/180, ALFA)
del(T)₅=0.000 (0/180, ALFA)
delTTT=0.000 (0/180, ALFA)
delTT=0.000 (0/180, ALFA)
delT=0.000 (0/180, ALFA)
dupT=0.000 (0/180, ALFA)
dupTT=0.000 (0/180, ALFA)
dupTTT=0.000 (0/180, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CDK8 : 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	180	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
European	Sub	16	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African	Sub	158	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	150	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTT=0, TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTT=0, TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTT=0, TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTT=0, TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	2	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTT=0, TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	4	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=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
Allele Frequency Aggregator	Total	Global	180	(T)₂₀=1.000	del(T)₁₅=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	African	Sub	158	(T)₂₀=1.000	del(T)₁₅=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	European	Sub	16	(T)₂₀=1.00	del(T)₁₅=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Other	Sub	4	(T)₂₀=1.0	del(T)₁₅=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0
Allele Frequency Aggregator	Latin American 2	Sub	2	(T)₂₀=1.0	del(T)₁₅=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₀=0	del(T)₁₅=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₀=0	del(T)₁₅=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₂₀=0	del(T)₁₅=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=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 13	NC_000013.11:g.26369715_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369718_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369719_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369720_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369721_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369722_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369723_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369724_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369725_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369726_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369727_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369728_26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369729del
GRCh38.p14 chr 13	NC_000013.11:g.26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369728_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369727_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369726_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369725_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369724_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369723_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369722_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369721_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369720_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369719_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369718_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369717_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369716_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369715_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369714_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369713_26369729dup
GRCh38.p14 chr 13	NC_000013.11:g.26369712_26369729dup
GRCh37.p13 chr 13	NC_000013.10:g.26943852_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943855_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943856_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943857_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943858_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943859_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943860_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943861_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943862_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943863_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943864_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943865_26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943866del
GRCh37.p13 chr 13	NC_000013.10:g.26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943865_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943864_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943863_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943862_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943861_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943860_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943859_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943858_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943857_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943856_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943855_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943854_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943853_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943852_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943851_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943850_26943866dup
GRCh37.p13 chr 13	NC_000013.10:g.26943849_26943866dup

Gene: CDK8, cyclin dependent kinase 8 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CDK8 transcript variant 1	NM_001260.3:c.457-13099_4… NM_001260.3:c.457-13099_457-13085del	N/A	Intron Variant
CDK8 transcript variant 2	NM_001318368.2:c.457-1309… NM_001318368.2:c.457-13099_457-13085del	N/A	Intron Variant
CDK8 transcript variant 3	NM_001346501.2:c.-5-15496… NM_001346501.2:c.-5-15496_-5-15482del	N/A	Intron Variant
CDK8 transcript variant X1	XM_047430033.1:c.277-1309… XM_047430033.1:c.277-13099_277-13085del	N/A	Intron Variant
CDK8 transcript variant X2	XM_011534865.3:c.	N/A	Genic Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₀=	del(T)₁₅	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈
GRCh38.p14 chr 13	NC_000013.11:g.26369710_26369729=	NC_000013.11:g.26369715_26369729del	NC_000013.11:g.26369718_26369729del	NC_000013.11:g.26369719_26369729del	NC_000013.11:g.26369720_26369729del	NC_000013.11:g.26369721_26369729del	NC_000013.11:g.26369722_26369729del	NC_000013.11:g.26369723_26369729del	NC_000013.11:g.26369724_26369729del	NC_000013.11:g.26369725_26369729del	NC_000013.11:g.26369726_26369729del	NC_000013.11:g.26369727_26369729del	NC_000013.11:g.26369728_26369729del	NC_000013.11:g.26369729del	NC_000013.11:g.26369729dup	NC_000013.11:g.26369728_26369729dup	NC_000013.11:g.26369727_26369729dup	NC_000013.11:g.26369726_26369729dup	NC_000013.11:g.26369725_26369729dup	NC_000013.11:g.26369724_26369729dup	NC_000013.11:g.26369723_26369729dup	NC_000013.11:g.26369722_26369729dup	NC_000013.11:g.26369721_26369729dup	NC_000013.11:g.26369720_26369729dup	NC_000013.11:g.26369719_26369729dup	NC_000013.11:g.26369718_26369729dup	NC_000013.11:g.26369717_26369729dup	NC_000013.11:g.26369716_26369729dup	NC_000013.11:g.26369715_26369729dup	NC_000013.11:g.26369714_26369729dup	NC_000013.11:g.26369713_26369729dup	NC_000013.11:g.26369712_26369729dup
GRCh37.p13 chr 13	NC_000013.10:g.26943847_26943866=	NC_000013.10:g.26943852_26943866del	NC_000013.10:g.26943855_26943866del	NC_000013.10:g.26943856_26943866del	NC_000013.10:g.26943857_26943866del	NC_000013.10:g.26943858_26943866del	NC_000013.10:g.26943859_26943866del	NC_000013.10:g.26943860_26943866del	NC_000013.10:g.26943861_26943866del	NC_000013.10:g.26943862_26943866del	NC_000013.10:g.26943863_26943866del	NC_000013.10:g.26943864_26943866del	NC_000013.10:g.26943865_26943866del	NC_000013.10:g.26943866del	NC_000013.10:g.26943866dup	NC_000013.10:g.26943865_26943866dup	NC_000013.10:g.26943864_26943866dup	NC_000013.10:g.26943863_26943866dup	NC_000013.10:g.26943862_26943866dup	NC_000013.10:g.26943861_26943866dup	NC_000013.10:g.26943860_26943866dup	NC_000013.10:g.26943859_26943866dup	NC_000013.10:g.26943858_26943866dup	NC_000013.10:g.26943857_26943866dup	NC_000013.10:g.26943856_26943866dup	NC_000013.10:g.26943855_26943866dup	NC_000013.10:g.26943854_26943866dup	NC_000013.10:g.26943853_26943866dup	NC_000013.10:g.26943852_26943866dup	NC_000013.10:g.26943851_26943866dup	NC_000013.10:g.26943850_26943866dup	NC_000013.10:g.26943849_26943866dup
CDK8 transcript	NM_001260.1:c.457-13104=	NM_001260.1:c.457-13099_457-13085del	NM_001260.1:c.457-13096_457-13085del	NM_001260.1:c.457-13095_457-13085del	NM_001260.1:c.457-13094_457-13085del	NM_001260.1:c.457-13093_457-13085del	NM_001260.1:c.457-13092_457-13085del	NM_001260.1:c.457-13091_457-13085del	NM_001260.1:c.457-13090_457-13085del	NM_001260.1:c.457-13089_457-13085del	NM_001260.1:c.457-13088_457-13085del	NM_001260.1:c.457-13087_457-13085del	NM_001260.1:c.457-13086_457-13085del	NM_001260.1:c.457-13085del	NM_001260.1:c.457-13085dup	NM_001260.1:c.457-13086_457-13085dup	NM_001260.1:c.457-13087_457-13085dup	NM_001260.1:c.457-13088_457-13085dup	NM_001260.1:c.457-13089_457-13085dup	NM_001260.1:c.457-13090_457-13085dup	NM_001260.1:c.457-13091_457-13085dup	NM_001260.1:c.457-13092_457-13085dup	NM_001260.1:c.457-13093_457-13085dup	NM_001260.1:c.457-13094_457-13085dup	NM_001260.1:c.457-13095_457-13085dup	NM_001260.1:c.457-13096_457-13085dup	NM_001260.1:c.457-13097_457-13085dup	NM_001260.1:c.457-13098_457-13085dup	NM_001260.1:c.457-13099_457-13085dup	NM_001260.1:c.457-13100_457-13085dup	NM_001260.1:c.457-13101_457-13085dup	NM_001260.1:c.457-13102_457-13085dup
CDK8 transcript variant 1	NM_001260.3:c.457-13104=	NM_001260.3:c.457-13099_457-13085del	NM_001260.3:c.457-13096_457-13085del	NM_001260.3:c.457-13095_457-13085del	NM_001260.3:c.457-13094_457-13085del	NM_001260.3:c.457-13093_457-13085del	NM_001260.3:c.457-13092_457-13085del	NM_001260.3:c.457-13091_457-13085del	NM_001260.3:c.457-13090_457-13085del	NM_001260.3:c.457-13089_457-13085del	NM_001260.3:c.457-13088_457-13085del	NM_001260.3:c.457-13087_457-13085del	NM_001260.3:c.457-13086_457-13085del	NM_001260.3:c.457-13085del	NM_001260.3:c.457-13085dup	NM_001260.3:c.457-13086_457-13085dup	NM_001260.3:c.457-13087_457-13085dup	NM_001260.3:c.457-13088_457-13085dup	NM_001260.3:c.457-13089_457-13085dup	NM_001260.3:c.457-13090_457-13085dup	NM_001260.3:c.457-13091_457-13085dup	NM_001260.3:c.457-13092_457-13085dup	NM_001260.3:c.457-13093_457-13085dup	NM_001260.3:c.457-13094_457-13085dup	NM_001260.3:c.457-13095_457-13085dup	NM_001260.3:c.457-13096_457-13085dup	NM_001260.3:c.457-13097_457-13085dup	NM_001260.3:c.457-13098_457-13085dup	NM_001260.3:c.457-13099_457-13085dup	NM_001260.3:c.457-13100_457-13085dup	NM_001260.3:c.457-13101_457-13085dup	NM_001260.3:c.457-13102_457-13085dup
CDK8 transcript variant 2	NM_001318368.2:c.457-13104=	NM_001318368.2:c.457-13099_457-13085del	NM_001318368.2:c.457-13096_457-13085del	NM_001318368.2:c.457-13095_457-13085del	NM_001318368.2:c.457-13094_457-13085del	NM_001318368.2:c.457-13093_457-13085del	NM_001318368.2:c.457-13092_457-13085del	NM_001318368.2:c.457-13091_457-13085del	NM_001318368.2:c.457-13090_457-13085del	NM_001318368.2:c.457-13089_457-13085del	NM_001318368.2:c.457-13088_457-13085del	NM_001318368.2:c.457-13087_457-13085del	NM_001318368.2:c.457-13086_457-13085del	NM_001318368.2:c.457-13085del	NM_001318368.2:c.457-13085dup	NM_001318368.2:c.457-13086_457-13085dup	NM_001318368.2:c.457-13087_457-13085dup	NM_001318368.2:c.457-13088_457-13085dup	NM_001318368.2:c.457-13089_457-13085dup	NM_001318368.2:c.457-13090_457-13085dup	NM_001318368.2:c.457-13091_457-13085dup	NM_001318368.2:c.457-13092_457-13085dup	NM_001318368.2:c.457-13093_457-13085dup	NM_001318368.2:c.457-13094_457-13085dup	NM_001318368.2:c.457-13095_457-13085dup	NM_001318368.2:c.457-13096_457-13085dup	NM_001318368.2:c.457-13097_457-13085dup	NM_001318368.2:c.457-13098_457-13085dup	NM_001318368.2:c.457-13099_457-13085dup	NM_001318368.2:c.457-13100_457-13085dup	NM_001318368.2:c.457-13101_457-13085dup	NM_001318368.2:c.457-13102_457-13085dup
CDK8 transcript variant 3	NM_001346501.2:c.-5-15501=	NM_001346501.2:c.-5-15496_-5-15482del	NM_001346501.2:c.-5-15493_-5-15482del	NM_001346501.2:c.-5-15492_-5-15482del	NM_001346501.2:c.-5-15491_-5-15482del	NM_001346501.2:c.-5-15490_-5-15482del	NM_001346501.2:c.-5-15489_-5-15482del	NM_001346501.2:c.-5-15488_-5-15482del	NM_001346501.2:c.-5-15487_-5-15482del	NM_001346501.2:c.-5-15486_-5-15482del	NM_001346501.2:c.-5-15485_-5-15482del	NM_001346501.2:c.-5-15484_-5-15482del	NM_001346501.2:c.-5-15483_-5-15482del	NM_001346501.2:c.-5-15482del	NM_001346501.2:c.-5-15482dup	NM_001346501.2:c.-5-15483_-5-15482dup	NM_001346501.2:c.-5-15484_-5-15482dup	NM_001346501.2:c.-5-15485_-5-15482dup	NM_001346501.2:c.-5-15486_-5-15482dup	NM_001346501.2:c.-5-15487_-5-15482dup	NM_001346501.2:c.-5-15488_-5-15482dup	NM_001346501.2:c.-5-15489_-5-15482dup	NM_001346501.2:c.-5-15490_-5-15482dup	NM_001346501.2:c.-5-15491_-5-15482dup	NM_001346501.2:c.-5-15492_-5-15482dup	NM_001346501.2:c.-5-15493_-5-15482dup	NM_001346501.2:c.-5-15494_-5-15482dup	NM_001346501.2:c.-5-15495_-5-15482dup	NM_001346501.2:c.-5-15496_-5-15482dup	NM_001346501.2:c.-5-15497_-5-15482dup	NM_001346501.2:c.-5-15498_-5-15482dup	NM_001346501.2:c.-5-15499_-5-15482dup
CDK8 transcript variant X1	XM_005266215.1:c.457-13104=	XM_005266215.1:c.457-13099_457-13085del	XM_005266215.1:c.457-13096_457-13085del	XM_005266215.1:c.457-13095_457-13085del	XM_005266215.1:c.457-13094_457-13085del	XM_005266215.1:c.457-13093_457-13085del	XM_005266215.1:c.457-13092_457-13085del	XM_005266215.1:c.457-13091_457-13085del	XM_005266215.1:c.457-13090_457-13085del	XM_005266215.1:c.457-13089_457-13085del	XM_005266215.1:c.457-13088_457-13085del	XM_005266215.1:c.457-13087_457-13085del	XM_005266215.1:c.457-13086_457-13085del	XM_005266215.1:c.457-13085del	XM_005266215.1:c.457-13085dup	XM_005266215.1:c.457-13086_457-13085dup	XM_005266215.1:c.457-13087_457-13085dup	XM_005266215.1:c.457-13088_457-13085dup	XM_005266215.1:c.457-13089_457-13085dup	XM_005266215.1:c.457-13090_457-13085dup	XM_005266215.1:c.457-13091_457-13085dup	XM_005266215.1:c.457-13092_457-13085dup	XM_005266215.1:c.457-13093_457-13085dup	XM_005266215.1:c.457-13094_457-13085dup	XM_005266215.1:c.457-13095_457-13085dup	XM_005266215.1:c.457-13096_457-13085dup	XM_005266215.1:c.457-13097_457-13085dup	XM_005266215.1:c.457-13098_457-13085dup	XM_005266215.1:c.457-13099_457-13085dup	XM_005266215.1:c.457-13100_457-13085dup	XM_005266215.1:c.457-13101_457-13085dup	XM_005266215.1:c.457-13102_457-13085dup
CDK8 transcript variant X2	XM_005266216.1:c.277-13104=	XM_005266216.1:c.277-13099_277-13085del	XM_005266216.1:c.277-13096_277-13085del	XM_005266216.1:c.277-13095_277-13085del	XM_005266216.1:c.277-13094_277-13085del	XM_005266216.1:c.277-13093_277-13085del	XM_005266216.1:c.277-13092_277-13085del	XM_005266216.1:c.277-13091_277-13085del	XM_005266216.1:c.277-13090_277-13085del	XM_005266216.1:c.277-13089_277-13085del	XM_005266216.1:c.277-13088_277-13085del	XM_005266216.1:c.277-13087_277-13085del	XM_005266216.1:c.277-13086_277-13085del	XM_005266216.1:c.277-13085del	XM_005266216.1:c.277-13085dup	XM_005266216.1:c.277-13086_277-13085dup	XM_005266216.1:c.277-13087_277-13085dup	XM_005266216.1:c.277-13088_277-13085dup	XM_005266216.1:c.277-13089_277-13085dup	XM_005266216.1:c.277-13090_277-13085dup	XM_005266216.1:c.277-13091_277-13085dup	XM_005266216.1:c.277-13092_277-13085dup	XM_005266216.1:c.277-13093_277-13085dup	XM_005266216.1:c.277-13094_277-13085dup	XM_005266216.1:c.277-13095_277-13085dup	XM_005266216.1:c.277-13096_277-13085dup	XM_005266216.1:c.277-13097_277-13085dup	XM_005266216.1:c.277-13098_277-13085dup	XM_005266216.1:c.277-13099_277-13085dup	XM_005266216.1:c.277-13100_277-13085dup	XM_005266216.1:c.277-13101_277-13085dup	XM_005266216.1:c.277-13102_277-13085dup
CDK8 transcript variant X1	XM_047430033.1:c.277-13104=	XM_047430033.1:c.277-13099_277-13085del	XM_047430033.1:c.277-13096_277-13085del	XM_047430033.1:c.277-13095_277-13085del	XM_047430033.1:c.277-13094_277-13085del	XM_047430033.1:c.277-13093_277-13085del	XM_047430033.1:c.277-13092_277-13085del	XM_047430033.1:c.277-13091_277-13085del	XM_047430033.1:c.277-13090_277-13085del	XM_047430033.1:c.277-13089_277-13085del	XM_047430033.1:c.277-13088_277-13085del	XM_047430033.1:c.277-13087_277-13085del	XM_047430033.1:c.277-13086_277-13085del	XM_047430033.1:c.277-13085del	XM_047430033.1:c.277-13085dup	XM_047430033.1:c.277-13086_277-13085dup	XM_047430033.1:c.277-13087_277-13085dup	XM_047430033.1:c.277-13088_277-13085dup	XM_047430033.1:c.277-13089_277-13085dup	XM_047430033.1:c.277-13090_277-13085dup	XM_047430033.1:c.277-13091_277-13085dup	XM_047430033.1:c.277-13092_277-13085dup	XM_047430033.1:c.277-13093_277-13085dup	XM_047430033.1:c.277-13094_277-13085dup	XM_047430033.1:c.277-13095_277-13085dup	XM_047430033.1:c.277-13096_277-13085dup	XM_047430033.1:c.277-13097_277-13085dup	XM_047430033.1:c.277-13098_277-13085dup	XM_047430033.1:c.277-13099_277-13085dup	XM_047430033.1:c.277-13100_277-13085dup	XM_047430033.1:c.277-13101_277-13085dup	XM_047430033.1:c.277-13102_277-13085dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

59 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40371948	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95615066	Feb 13, 2009 (130)
3	BCMHGSC_JDW	ss103543555	Mar 15, 2016 (147)
4	PJP	ss294788134	May 09, 2011 (134)
5	SSMP	ss664168168	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1707718270	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1707718362	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710593354	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710593356	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710593361	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710593363	Apr 01, 2015 (144)
12	SWEGEN	ss3010746054	Jan 10, 2018 (151)
13	MCHAISSO	ss3064588128	Jan 10, 2018 (151)
14	EVA_DECODE	ss3694956302	Jul 13, 2019 (153)
15	EVA_DECODE	ss3694956303	Jul 13, 2019 (153)
16	EVA_DECODE	ss3694956304	Jul 13, 2019 (153)
17	EVA_DECODE	ss3694956305	Jul 13, 2019 (153)
18	PACBIO	ss3787409098	Jul 13, 2019 (153)
19	PACBIO	ss3792482462	Jul 13, 2019 (153)
20	PACBIO	ss3797366184	Jul 13, 2019 (153)
21	EVA	ss3833456970	Apr 27, 2020 (154)
22	GNOMAD	ss4262972428	Apr 26, 2021 (155)
23	GNOMAD	ss4262972429	Apr 26, 2021 (155)
24	GNOMAD	ss4262972430	Apr 26, 2021 (155)
25	GNOMAD	ss4262972431	Apr 26, 2021 (155)
26	GNOMAD	ss4262972432	Apr 26, 2021 (155)
27	GNOMAD	ss4262972433	Apr 26, 2021 (155)
28	GNOMAD	ss4262972434	Apr 26, 2021 (155)
29	GNOMAD	ss4262972435	Apr 26, 2021 (155)
30	GNOMAD	ss4262972436	Apr 26, 2021 (155)
31	GNOMAD	ss4262972437	Apr 26, 2021 (155)
32	GNOMAD	ss4262972438	Apr 26, 2021 (155)
33	GNOMAD	ss4262972439	Apr 26, 2021 (155)
34	GNOMAD	ss4262972440	Apr 26, 2021 (155)
35	GNOMAD	ss4262972441	Apr 26, 2021 (155)
36	GNOMAD	ss4262972442	Apr 26, 2021 (155)
37	GNOMAD	ss4262972443	Apr 26, 2021 (155)
38	GNOMAD	ss4262972444	Apr 26, 2021 (155)
39	GNOMAD	ss4262972445	Apr 26, 2021 (155)
40	GNOMAD	ss4262972446	Apr 26, 2021 (155)
41	GNOMAD	ss4262972447	Apr 26, 2021 (155)
42	GNOMAD	ss4262972448	Apr 26, 2021 (155)
43	GNOMAD	ss4262972449	Apr 26, 2021 (155)
44	GNOMAD	ss4262972450	Apr 26, 2021 (155)
45	GNOMAD	ss4262972451	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5209242760	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5209242761	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5209242762	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5209242763	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5209242764	Apr 26, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5293149084	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5293149085	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5487569684	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5487569685	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5760902201	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5760902202	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5760902203	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5760902205	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5760902206	Oct 16, 2022 (156)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33543140 (NC_000013.10:26943847:T: 1591/3854) Row 33543141 (NC_000013.10:26943846:TTT: 166/3854)	-	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33543140 (NC_000013.10:26943847:T: 1591/3854) Row 33543141 (NC_000013.10:26943846:TTT: 166/3854)	-	Oct 12, 2018 (152)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425911692 (NC_000013.11:26369709::T 935/88590) Row 425911693 (NC_000013.11:26369709::TT 54/88578) Row 425911694 (NC_000013.11:26369709::TTT 42/88570)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 67212067 (NC_000013.10:26943846:T: 12444/16542) Row 67212068 (NC_000013.10:26943846:TT: 154/16542) Row 67212069 (NC_000013.10:26943846:TTTTTTTT: 26/16542)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 67212067 (NC_000013.10:26943846:T: 12444/16542) Row 67212068 (NC_000013.10:26943846:TT: 154/16542) Row 67212069 (NC_000013.10:26943846:TTTTTTTT: 26/16542)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 67212067 (NC_000013.10:26943846:T: 12444/16542) Row 67212068 (NC_000013.10:26943846:TT: 154/16542) Row 67212069 (NC_000013.10:26943846:TTTTTTTT: 26/16542)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 67212067 (NC_000013.10:26943846:T: 12444/16542) Row 67212068 (NC_000013.10:26943846:TT: 154/16542) Row 67212069 (NC_000013.10:26943846:TTTTTTTT: 26/16542)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 67212067 (NC_000013.10:26943846:T: 12444/16542) Row 67212068 (NC_000013.10:26943846:TT: 154/16542) Row 67212069 (NC_000013.10:26943846:TTTTTTTT: 26/16542)...	-	Apr 26, 2021 (155)
91	14KJPN Submission ignored due to conflicting rows: Row 94739305 (NC_000013.11:26369709:T: 21150/26544) Row 94739306 (NC_000013.11:26369709:TT: 250/26544) Row 94739307 (NC_000013.11:26369709:TTTTTTTT: 43/26544)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 94739305 (NC_000013.11:26369709:T: 21150/26544) Row 94739306 (NC_000013.11:26369709:TT: 250/26544) Row 94739307 (NC_000013.11:26369709:TTTTTTTT: 43/26544)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 94739305 (NC_000013.11:26369709:T: 21150/26544) Row 94739306 (NC_000013.11:26369709:TT: 250/26544) Row 94739307 (NC_000013.11:26369709:TTTTTTTT: 43/26544)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 94739305 (NC_000013.11:26369709:T: 21150/26544) Row 94739306 (NC_000013.11:26369709:TT: 250/26544) Row 94739307 (NC_000013.11:26369709:TTTTTTTT: 43/26544)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 94739305 (NC_000013.11:26369709:T: 21150/26544) Row 94739306 (NC_000013.11:26369709:TT: 250/26544) Row 94739307 (NC_000013.11:26369709:TTTTTTTT: 43/26544)...	-	Oct 16, 2022 (156)
96	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33543139 (NC_000013.10:26943848:T: 2008/3708) Row 33543140 (NC_000013.10:26943847:TT: 1540/3708) Row 33543141 (NC_000013.10:26943846:TTT: 131/3708)	-	Apr 27, 2020 (154)
97	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33543140 (NC_000013.10:26943847:T: 1540/3708) Row 33543141 (NC_000013.10:26943846:TTT: 131/3708)	-	Oct 12, 2018 (152)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33543140 (NC_000013.10:26943847:T: 1540/3708) Row 33543141 (NC_000013.10:26943846:TTT: 131/3708)	-	Oct 12, 2018 (152)
99	ALFA	NC_000013.11 - 26369710	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)
rs77457824	Oct 17, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4262972451	NC_000013.11:26369709:TTTTTTTTTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4262972450	NC_000013.11:26369709:TTTTTTTTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5209242762	NC_000013.10:26943846:TTTTTTTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5760902203	NC_000013.11:26369709:TTTTTTTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4262972449	NC_000013.11:26369709:TTTTTTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4262972448	NC_000013.11:26369709:TTTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss103543555	NT_024524.14:7923862:TTTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss1707718270, ss1707718362	NC_000013.10:26943846:TTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3694956302, ss4262972447	NC_000013.11:26369709:TTT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3010746054, ss5209242761	NC_000013.10:26943846:TT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1710593356, ss1710593363	NC_000013.10:26943847:TT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3064588128, ss4262972446, ss5293149085, ss5760902202	NC_000013.11:26369709:TT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3694956303	NC_000013.11:26369710:TT:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss294788134	NC_000013.9:25841846:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3787409098, ss3792482462, ss3797366184, ss3833456970, ss5209242760	NC_000013.10:26943846:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
	NC_000013.10:26943847:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss1710593354, ss1710593361	NC_000013.10:26943848:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5487569684, ss5760902201	NC_000013.11:26369709:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3694956304	NC_000013.11:26369711:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss40371948	NT_024524.14:7923846:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss95615066	NT_024524.14:7923865:T:	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss664168168	NC_000013.10:26943846::T	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972428, ss5293149084, ss5487569685	NC_000013.11:26369709::T	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972429	NC_000013.11:26369709::TT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972430	NC_000013.11:26369709::TTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7784505706	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3694956305	NC_000013.11:26369712::TTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972431	NC_000013.11:26369709::TTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972432	NC_000013.11:26369709::TTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972433	NC_000013.11:26369709::TTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5209242763	NC_000013.10:26943846::TTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972434, ss5760902205	NC_000013.11:26369709::TTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5209242764	NC_000013.10:26943846::TTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972435, ss5760902206	NC_000013.11:26369709::TTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972436	NC_000013.11:26369709::TTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972437	NC_000013.11:26369709::TTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972438	NC_000013.11:26369709::TTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972439	NC_000013.11:26369709::TTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972440	NC_000013.11:26369709::TTTTTTTTTTT… NC_000013.11:26369709::TTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972441	NC_000013.11:26369709::TTTTTTTTTTT… NC_000013.11:26369709::TTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972442	NC_000013.11:26369709::TTTTTTTTTTT… NC_000013.11:26369709::TTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972443	NC_000013.11:26369709::TTTTTTTTTTT… NC_000013.11:26369709::TTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972444	NC_000013.11:26369709::TTTTTTTTTTT… NC_000013.11:26369709::TTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4262972445	NC_000013.11:26369709::TTTTTTTTTTT… NC_000013.11:26369709::TTTTTTTTTTTTTTTTTT	NC_000013.11:26369709:TTTTTTTTTTTT… NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs36116401

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

rs36116401