Name: rs71188725
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.

rs71188725

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:26363328-26363341 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₂ / dup(A)₁₃ / dup(A)₁₄ / ins(A)₁₅ / ins(A)₁₆ / ins(A)₁₇ / ins(A)₁₈ / ins(A)₁₉ / ins(A)₂₃ / ins(A)₂₅
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.0000 (0/1004, ALFA)
delAA=0.0000 (0/1004, ALFA)
delA=0.0000 (0/1004, ALFA) (+ 19 more)
dupA=0.0000 (0/1004, ALFA)
dupAA=0.0000 (0/1004, ALFA)
dupAAA=0.0000 (0/1004, ALFA)
dup(A)₄=0.0000 (0/1004, ALFA)
dup(A)₅=0.0000 (0/1004, ALFA)
dup(A)₆=0.0000 (0/1004, ALFA)
dup(A)₇=0.0000 (0/1004, ALFA)
dup(A)₈=0.0000 (0/1004, ALFA)
dup(A)₉=0.0000 (0/1004, ALFA)
dup(A)₁₀=0.0000 (0/1004, ALFA)
dup(A)₁₁=0.0000 (0/1004, ALFA)
dup(A)₁₂=0.0000 (0/1004, ALFA)
dup(A)₁₃=0.0000 (0/1004, ALFA)
dup(A)₁₄=0.0000 (0/1004, ALFA)
ins(A)₁₅=0.0000 (0/1004, ALFA)
ins(A)₁₆=0.0000 (0/1004, ALFA)
ins(A)₁₇=0.0000 (0/1004, ALFA)
ins(A)₁₈=0.0000 (0/1004, ALFA)
ins(A)₁₉=0.0000 (0/1004, 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	1004	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	772	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	138	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	AAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	134	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	14	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	32	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	36	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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
Allele Frequency Aggregator	Total	Global	1004	(A)₁₄=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000, dup(A)₇=0.0000, dup(A)₈=0.0000, dup(A)₉=0.0000, dup(A)₁₀=0.0000, dup(A)₁₁=0.0000, dup(A)₁₂=0.0000, dup(A)₁₃=0.0000, dup(A)₁₄=0.0000, ins(A)₁₅=0.0000, ins(A)₁₆=0.0000, ins(A)₁₇=0.0000, ins(A)₁₈=0.0000, ins(A)₁₉=0.0000
Allele Frequency Aggregator	European	Sub	772	(A)₁₄=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000, dup(A)₈=0.000, dup(A)₉=0.000, dup(A)₁₀=0.000, dup(A)₁₁=0.000, dup(A)₁₂=0.000, dup(A)₁₃=0.000, dup(A)₁₄=0.000, ins(A)₁₅=0.000, ins(A)₁₆=0.000, ins(A)₁₇=0.000, ins(A)₁₈=0.000, ins(A)₁₉=0.000
Allele Frequency Aggregator	African	Sub	138	(A)₁₄=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000, dup(A)₈=0.000, dup(A)₉=0.000, dup(A)₁₀=0.000, dup(A)₁₁=0.000, dup(A)₁₂=0.000, dup(A)₁₃=0.000, dup(A)₁₄=0.000, ins(A)₁₅=0.000, ins(A)₁₆=0.000, ins(A)₁₇=0.000, ins(A)₁₈=0.000, ins(A)₁₉=0.000
Allele Frequency Aggregator	Other	Sub	36	(A)₁₄=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00, dup(A)₁₀=0.00, dup(A)₁₁=0.00, dup(A)₁₂=0.00, dup(A)₁₃=0.00, dup(A)₁₄=0.00, ins(A)₁₅=0.00, ins(A)₁₆=0.00, ins(A)₁₇=0.00, ins(A)₁₈=0.00, ins(A)₁₉=0.00
Allele Frequency Aggregator	Latin American 2	Sub	32	(A)₁₄=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00, dup(A)₁₀=0.00, dup(A)₁₁=0.00, dup(A)₁₂=0.00, dup(A)₁₃=0.00, dup(A)₁₄=0.00, ins(A)₁₅=0.00, ins(A)₁₆=0.00, ins(A)₁₇=0.00, ins(A)₁₈=0.00, ins(A)₁₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(A)₁₄=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00, dup(A)₁₀=0.00, dup(A)₁₁=0.00, dup(A)₁₂=0.00, dup(A)₁₃=0.00, dup(A)₁₄=0.00, ins(A)₁₅=0.00, ins(A)₁₆=0.00, ins(A)₁₇=0.00, ins(A)₁₈=0.00, ins(A)₁₉=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(A)₁₄=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00, dup(A)₁₀=0.00, dup(A)₁₁=0.00, dup(A)₁₂=0.00, dup(A)₁₃=0.00, dup(A)₁₄=0.00, ins(A)₁₅=0.00, ins(A)₁₆=0.00, ins(A)₁₇=0.00, ins(A)₁₈=0.00, ins(A)₁₉=0.00
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₄=0	delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0, dup(A)₆=0, dup(A)₇=0, dup(A)₈=0, dup(A)₉=0, dup(A)₁₀=0, dup(A)₁₁=0, dup(A)₁₂=0, dup(A)₁₃=0, dup(A)₁₄=0, ins(A)₁₅=0, ins(A)₁₆=0, ins(A)₁₇=0, ins(A)₁₈=0, ins(A)₁₉=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.26363339_26363341del
GRCh38.p14 chr 13	NC_000013.11:g.26363340_26363341del
GRCh38.p14 chr 13	NC_000013.11:g.26363341del
GRCh38.p14 chr 13	NC_000013.11:g.26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363340_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363339_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363338_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363337_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363336_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363335_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363334_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363333_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363332_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363331_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363330_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363329_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363328_26363341dup
GRCh38.p14 chr 13	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 13	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937476_26937478del
GRCh37.p13 chr 13	NC_000013.10:g.26937477_26937478del
GRCh37.p13 chr 13	NC_000013.10:g.26937478del
GRCh37.p13 chr 13	NC_000013.10:g.26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937477_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937476_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937475_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937474_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937473_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937472_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937471_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937470_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937469_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937468_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937467_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937466_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937465_26937478dup
GRCh37.p13 chr 13	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAAAAAAAA

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

Molecule type	Change	Amino acid[Codon]	SO Term
CDK8 transcript variant 1	NM_001260.3:c.456+9459_45… NM_001260.3:c.456+9459_456+9461del	N/A	Intron Variant
CDK8 transcript variant 2	NM_001318368.2:c.456+9459… NM_001318368.2:c.456+9459_456+9461del	N/A	Intron Variant
CDK8 transcript variant 3	NM_001346501.2:c.-6+9459_… NM_001346501.2:c.-6+9459_-6+9461del	N/A	Intron Variant
CDK8 transcript variant X1	XM_047430033.1:c.276+9459… XM_047430033.1:c.276+9459_276+9461del	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	(A)₁₄=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₂	dup(A)₁₃	dup(A)₁₄	ins(A)₁₅	ins(A)₁₆	ins(A)₁₇	ins(A)₁₈	ins(A)₁₉	ins(A)₂₃	ins(A)₂₅
GRCh38.p14 chr 13	NC_000013.11:g.26363328_26363341=	NC_000013.11:g.26363339_26363341del	NC_000013.11:g.26363340_26363341del	NC_000013.11:g.26363341del	NC_000013.11:g.26363341dup	NC_000013.11:g.26363340_26363341dup	NC_000013.11:g.26363339_26363341dup	NC_000013.11:g.26363338_26363341dup	NC_000013.11:g.26363337_26363341dup	NC_000013.11:g.26363336_26363341dup	NC_000013.11:g.26363335_26363341dup	NC_000013.11:g.26363334_26363341dup	NC_000013.11:g.26363333_26363341dup	NC_000013.11:g.26363332_26363341dup	NC_000013.11:g.26363331_26363341dup	NC_000013.11:g.26363330_26363341dup	NC_000013.11:g.26363329_26363341dup	NC_000013.11:g.26363328_26363341dup	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAA	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAA	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAA	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAA	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAA	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 13	NC_000013.10:g.26937465_26937478=	NC_000013.10:g.26937476_26937478del	NC_000013.10:g.26937477_26937478del	NC_000013.10:g.26937478del	NC_000013.10:g.26937478dup	NC_000013.10:g.26937477_26937478dup	NC_000013.10:g.26937476_26937478dup	NC_000013.10:g.26937475_26937478dup	NC_000013.10:g.26937474_26937478dup	NC_000013.10:g.26937473_26937478dup	NC_000013.10:g.26937472_26937478dup	NC_000013.10:g.26937471_26937478dup	NC_000013.10:g.26937470_26937478dup	NC_000013.10:g.26937469_26937478dup	NC_000013.10:g.26937468_26937478dup	NC_000013.10:g.26937467_26937478dup	NC_000013.10:g.26937466_26937478dup	NC_000013.10:g.26937465_26937478dup	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAA	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAA	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAA	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAA	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAA	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAAAAAAAA
CDK8 transcript	NM_001260.1:c.456+9448=	NM_001260.1:c.456+9459_456+9461del	NM_001260.1:c.456+9460_456+9461del	NM_001260.1:c.456+9461del	NM_001260.1:c.456+9461dup	NM_001260.1:c.456+9460_456+9461dup	NM_001260.1:c.456+9459_456+9461dup	NM_001260.1:c.456+9458_456+9461dup	NM_001260.1:c.456+9457_456+9461dup	NM_001260.1:c.456+9456_456+9461dup	NM_001260.1:c.456+9455_456+9461dup	NM_001260.1:c.456+9454_456+9461dup	NM_001260.1:c.456+9453_456+9461dup	NM_001260.1:c.456+9452_456+9461dup	NM_001260.1:c.456+9451_456+9461dup	NM_001260.1:c.456+9450_456+9461dup	NM_001260.1:c.456+9449_456+9461dup	NM_001260.1:c.456+9448_456+9461dup	NM_001260.1:c.456+9461_456+9462insAAAAAAAAAAAAAAA	NM_001260.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAA	NM_001260.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAA	NM_001260.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAA	NM_001260.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAA	NM_001260.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAA	NM_001260.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAAAA
CDK8 transcript variant 1	NM_001260.3:c.456+9448=	NM_001260.3:c.456+9459_456+9461del	NM_001260.3:c.456+9460_456+9461del	NM_001260.3:c.456+9461del	NM_001260.3:c.456+9461dup	NM_001260.3:c.456+9460_456+9461dup	NM_001260.3:c.456+9459_456+9461dup	NM_001260.3:c.456+9458_456+9461dup	NM_001260.3:c.456+9457_456+9461dup	NM_001260.3:c.456+9456_456+9461dup	NM_001260.3:c.456+9455_456+9461dup	NM_001260.3:c.456+9454_456+9461dup	NM_001260.3:c.456+9453_456+9461dup	NM_001260.3:c.456+9452_456+9461dup	NM_001260.3:c.456+9451_456+9461dup	NM_001260.3:c.456+9450_456+9461dup	NM_001260.3:c.456+9449_456+9461dup	NM_001260.3:c.456+9448_456+9461dup	NM_001260.3:c.456+9461_456+9462insAAAAAAAAAAAAAAA	NM_001260.3:c.456+9461_456+9462insAAAAAAAAAAAAAAAA	NM_001260.3:c.456+9461_456+9462insAAAAAAAAAAAAAAAAA	NM_001260.3:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAA	NM_001260.3:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAA	NM_001260.3:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAA	NM_001260.3:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAAAA
CDK8 transcript variant 2	NM_001318368.2:c.456+9448=	NM_001318368.2:c.456+9459_456+9461del	NM_001318368.2:c.456+9460_456+9461del	NM_001318368.2:c.456+9461del	NM_001318368.2:c.456+9461dup	NM_001318368.2:c.456+9460_456+9461dup	NM_001318368.2:c.456+9459_456+9461dup	NM_001318368.2:c.456+9458_456+9461dup	NM_001318368.2:c.456+9457_456+9461dup	NM_001318368.2:c.456+9456_456+9461dup	NM_001318368.2:c.456+9455_456+9461dup	NM_001318368.2:c.456+9454_456+9461dup	NM_001318368.2:c.456+9453_456+9461dup	NM_001318368.2:c.456+9452_456+9461dup	NM_001318368.2:c.456+9451_456+9461dup	NM_001318368.2:c.456+9450_456+9461dup	NM_001318368.2:c.456+9449_456+9461dup	NM_001318368.2:c.456+9448_456+9461dup	NM_001318368.2:c.456+9461_456+9462insAAAAAAAAAAAAAAA	NM_001318368.2:c.456+9461_456+9462insAAAAAAAAAAAAAAAA	NM_001318368.2:c.456+9461_456+9462insAAAAAAAAAAAAAAAAA	NM_001318368.2:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAA	NM_001318368.2:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAA	NM_001318368.2:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAA	NM_001318368.2:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAAAA
CDK8 transcript variant 3	NM_001346501.2:c.-6+9448=	NM_001346501.2:c.-6+9459_-6+9461del	NM_001346501.2:c.-6+9460_-6+9461del	NM_001346501.2:c.-6+9461del	NM_001346501.2:c.-6+9461dup	NM_001346501.2:c.-6+9460_-6+9461dup	NM_001346501.2:c.-6+9459_-6+9461dup	NM_001346501.2:c.-6+9458_-6+9461dup	NM_001346501.2:c.-6+9457_-6+9461dup	NM_001346501.2:c.-6+9456_-6+9461dup	NM_001346501.2:c.-6+9455_-6+9461dup	NM_001346501.2:c.-6+9454_-6+9461dup	NM_001346501.2:c.-6+9453_-6+9461dup	NM_001346501.2:c.-6+9452_-6+9461dup	NM_001346501.2:c.-6+9451_-6+9461dup	NM_001346501.2:c.-6+9450_-6+9461dup	NM_001346501.2:c.-6+9449_-6+9461dup	NM_001346501.2:c.-6+9448_-6+9461dup	NM_001346501.2:c.-6+9461_-6+9462insAAAAAAAAAAAAAAA	NM_001346501.2:c.-6+9461_-6+9462insAAAAAAAAAAAAAAAA	NM_001346501.2:c.-6+9461_-6+9462insAAAAAAAAAAAAAAAAA	NM_001346501.2:c.-6+9461_-6+9462insAAAAAAAAAAAAAAAAAA	NM_001346501.2:c.-6+9461_-6+9462insAAAAAAAAAAAAAAAAAAA	NM_001346501.2:c.-6+9461_-6+9462insAAAAAAAAAAAAAAAAAAAAAAA	NM_001346501.2:c.-6+9461_-6+9462insAAAAAAAAAAAAAAAAAAAAAAAAA
CDK8 transcript variant X1	XM_005266215.1:c.456+9448=	XM_005266215.1:c.456+9459_456+9461del	XM_005266215.1:c.456+9460_456+9461del	XM_005266215.1:c.456+9461del	XM_005266215.1:c.456+9461dup	XM_005266215.1:c.456+9460_456+9461dup	XM_005266215.1:c.456+9459_456+9461dup	XM_005266215.1:c.456+9458_456+9461dup	XM_005266215.1:c.456+9457_456+9461dup	XM_005266215.1:c.456+9456_456+9461dup	XM_005266215.1:c.456+9455_456+9461dup	XM_005266215.1:c.456+9454_456+9461dup	XM_005266215.1:c.456+9453_456+9461dup	XM_005266215.1:c.456+9452_456+9461dup	XM_005266215.1:c.456+9451_456+9461dup	XM_005266215.1:c.456+9450_456+9461dup	XM_005266215.1:c.456+9449_456+9461dup	XM_005266215.1:c.456+9448_456+9461dup	XM_005266215.1:c.456+9461_456+9462insAAAAAAAAAAAAAAA	XM_005266215.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAA	XM_005266215.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAA	XM_005266215.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAA	XM_005266215.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAA	XM_005266215.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAA	XM_005266215.1:c.456+9461_456+9462insAAAAAAAAAAAAAAAAAAAAAAAAA
CDK8 transcript variant X2	XM_005266216.1:c.276+9448=	XM_005266216.1:c.276+9459_276+9461del	XM_005266216.1:c.276+9460_276+9461del	XM_005266216.1:c.276+9461del	XM_005266216.1:c.276+9461dup	XM_005266216.1:c.276+9460_276+9461dup	XM_005266216.1:c.276+9459_276+9461dup	XM_005266216.1:c.276+9458_276+9461dup	XM_005266216.1:c.276+9457_276+9461dup	XM_005266216.1:c.276+9456_276+9461dup	XM_005266216.1:c.276+9455_276+9461dup	XM_005266216.1:c.276+9454_276+9461dup	XM_005266216.1:c.276+9453_276+9461dup	XM_005266216.1:c.276+9452_276+9461dup	XM_005266216.1:c.276+9451_276+9461dup	XM_005266216.1:c.276+9450_276+9461dup	XM_005266216.1:c.276+9449_276+9461dup	XM_005266216.1:c.276+9448_276+9461dup	XM_005266216.1:c.276+9461_276+9462insAAAAAAAAAAAAAAA	XM_005266216.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAA	XM_005266216.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAA	XM_005266216.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAA	XM_005266216.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAAA	XM_005266216.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAAAAAAA	XM_005266216.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAAAAAAAAA
CDK8 transcript variant X1	XM_047430033.1:c.276+9448=	XM_047430033.1:c.276+9459_276+9461del	XM_047430033.1:c.276+9460_276+9461del	XM_047430033.1:c.276+9461del	XM_047430033.1:c.276+9461dup	XM_047430033.1:c.276+9460_276+9461dup	XM_047430033.1:c.276+9459_276+9461dup	XM_047430033.1:c.276+9458_276+9461dup	XM_047430033.1:c.276+9457_276+9461dup	XM_047430033.1:c.276+9456_276+9461dup	XM_047430033.1:c.276+9455_276+9461dup	XM_047430033.1:c.276+9454_276+9461dup	XM_047430033.1:c.276+9453_276+9461dup	XM_047430033.1:c.276+9452_276+9461dup	XM_047430033.1:c.276+9451_276+9461dup	XM_047430033.1:c.276+9450_276+9461dup	XM_047430033.1:c.276+9449_276+9461dup	XM_047430033.1:c.276+9448_276+9461dup	XM_047430033.1:c.276+9461_276+9462insAAAAAAAAAAAAAAA	XM_047430033.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAA	XM_047430033.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAA	XM_047430033.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAA	XM_047430033.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAAA	XM_047430033.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAAAAAAA	XM_047430033.1:c.276+9461_276+9462insAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

47 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82302002	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95615065	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss95762807	Feb 13, 2009 (130)
4	SWEGEN	ss3010745996	Nov 08, 2017 (151)
5	SWEGEN	ss3010745997	Nov 08, 2017 (151)
6	SWEGEN	ss3010745998	Nov 08, 2017 (151)
7	SWEGEN	ss3010745999	Nov 08, 2017 (151)
8	SWEGEN	ss3010746000	Nov 08, 2017 (151)
9	SWEGEN	ss3010746001	Nov 08, 2017 (151)
10	EVA_DECODE	ss3694956226	Jul 13, 2019 (153)
11	EVA_DECODE	ss3694956227	Jul 13, 2019 (153)
12	EVA_DECODE	ss3694956228	Jul 13, 2019 (153)
13	EVA_DECODE	ss3694956229	Jul 13, 2019 (153)
14	EVA_DECODE	ss3694956230	Jul 13, 2019 (153)
15	PACBIO	ss3787409089	Jul 13, 2019 (153)
16	PACBIO	ss3792482453	Jul 13, 2019 (153)
17	PACBIO	ss3792482454	Jul 13, 2019 (153)
18	PACBIO	ss3797366175	Jul 13, 2019 (153)
19	PACBIO	ss3797366176	Jul 13, 2019 (153)
20	EVA	ss3833456949	Apr 27, 2020 (154)
21	GNOMAD	ss4262971620	Apr 26, 2021 (155)
22	GNOMAD	ss4262971621	Apr 26, 2021 (155)
23	GNOMAD	ss4262971622	Apr 26, 2021 (155)
24	GNOMAD	ss4262971623	Apr 26, 2021 (155)
25	GNOMAD	ss4262971624	Apr 26, 2021 (155)
26	GNOMAD	ss4262971625	Apr 26, 2021 (155)
27	GNOMAD	ss4262971626	Apr 26, 2021 (155)
28	GNOMAD	ss4262971627	Apr 26, 2021 (155)
29	GNOMAD	ss4262971638	Apr 26, 2021 (155)
30	GNOMAD	ss4262971639	Apr 26, 2021 (155)
31	GNOMAD	ss4262971640	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5209242584	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5209242585	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5209242586	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5209242587	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5209242588	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5209242589	Apr 26, 2021 (155)
38	HUGCELL_USP	ss5487569556	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5487569557	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5487569558	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5487569559	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5760901902	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5760901903	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5760901904	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5760901905	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5760901906	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5760901907	Oct 16, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 425910398 (NC_000013.11:26363327::A 15/42928) Row 425910399 (NC_000013.11:26363327::AA 3/42926) Row 425910400 (NC_000013.11:26363327::AAA 78/42926)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 67211891 (NC_000013.10:26937464::AAAAAAAAAAAAA 4742/11128) Row 67211892 (NC_000013.10:26937464::AAAAAAAAAAAA 259/11128) Row 67211893 (NC_000013.10:26937464::AAAAAAAAA 613/11128)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 67211891 (NC_000013.10:26937464::AAAAAAAAAAAAA 4742/11128) Row 67211892 (NC_000013.10:26937464::AAAAAAAAAAAA 259/11128) Row 67211893 (NC_000013.10:26937464::AAAAAAAAA 613/11128)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 67211891 (NC_000013.10:26937464::AAAAAAAAAAAAA 4742/11128) Row 67211892 (NC_000013.10:26937464::AAAAAAAAAAAA 259/11128) Row 67211893 (NC_000013.10:26937464::AAAAAAAAA 613/11128)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 67211891 (NC_000013.10:26937464::AAAAAAAAAAAAA 4742/11128) Row 67211892 (NC_000013.10:26937464::AAAAAAAAAAAA 259/11128) Row 67211893 (NC_000013.10:26937464::AAAAAAAAA 613/11128)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 67211891 (NC_000013.10:26937464::AAAAAAAAAAAAA 4742/11128) Row 67211892 (NC_000013.10:26937464::AAAAAAAAAAAA 259/11128) Row 67211893 (NC_000013.10:26937464::AAAAAAAAA 613/11128)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 67211891 (NC_000013.10:26937464::AAAAAAAAAAAAA 4742/11128) Row 67211892 (NC_000013.10:26937464::AAAAAAAAAAAA 259/11128) Row 67211893 (NC_000013.10:26937464::AAAAAAAAA 613/11128)...	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 94739006 (NC_000013.11:26363327::AAAAAAAAAAAAA 9740/20746) Row 94739007 (NC_000013.11:26363327::AAAAAAAAAAAAAA 336/20746) Row 94739008 (NC_000013.11:26363327::AAAAAAAAAAAAAAAA 6227/20746)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 94739006 (NC_000013.11:26363327::AAAAAAAAAAAAA 9740/20746) Row 94739007 (NC_000013.11:26363327::AAAAAAAAAAAAAA 336/20746) Row 94739008 (NC_000013.11:26363327::AAAAAAAAAAAAAAAA 6227/20746)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 94739006 (NC_000013.11:26363327::AAAAAAAAAAAAA 9740/20746) Row 94739007 (NC_000013.11:26363327::AAAAAAAAAAAAAA 336/20746) Row 94739008 (NC_000013.11:26363327::AAAAAAAAAAAAAAAA 6227/20746)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 94739006 (NC_000013.11:26363327::AAAAAAAAAAAAA 9740/20746) Row 94739007 (NC_000013.11:26363327::AAAAAAAAAAAAAA 336/20746) Row 94739008 (NC_000013.11:26363327::AAAAAAAAAAAAAAAA 6227/20746)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 94739006 (NC_000013.11:26363327::AAAAAAAAAAAAA 9740/20746) Row 94739007 (NC_000013.11:26363327::AAAAAAAAAAAAAA 336/20746) Row 94739008 (NC_000013.11:26363327::AAAAAAAAAAAAAAAA 6227/20746)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 94739006 (NC_000013.11:26363327::AAAAAAAAAAAAA 9740/20746) Row 94739007 (NC_000013.11:26363327::AAAAAAAAAAAAAA 336/20746) Row 94739008 (NC_000013.11:26363327::AAAAAAAAAAAAAAAA 6227/20746)...	-	Oct 16, 2022 (156)
71	ALFA	NC_000013.11 - 26363328	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4262971640	NC_000013.11:26363327:AAA:	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4262971639	NC_000013.11:26363327:AA:	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4262971638	NC_000013.11:26363327:A:	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4262971620	NC_000013.11:26363327::A	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4262971621	NC_000013.11:26363327::AA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4262971622	NC_000013.11:26363327::AAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss95762807	NT_024524.14:7917464::AAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4262971623	NC_000013.11:26363327::AAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4262971624	NC_000013.11:26363327::AAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3833456949	NC_000013.10:26937464::AAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5209242586	NC_000013.10:26937464::AAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694956230, ss4262971625	NC_000013.11:26363327::AAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3787409089, ss3792482453, ss3797366175, ss5209242585	NC_000013.10:26937464::AAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694956229	NC_000013.11:26363327::AAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3010745996, ss3792482454, ss3797366176, ss5209242584	NC_000013.10:26937464::AAAAAAAAAAA… NC_000013.10:26937464::AAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694956228, ss5487569557, ss5760901902	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3010745997	NC_000013.10:26937464::AAAAAAAAAAA… NC_000013.10:26937464::AAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694956227, ss5487569558, ss5760901903	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3010746000, ss5209242588	NC_000013.10:26937464::AAAAAAAAAAA… NC_000013.10:26937464::AAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5487569559, ss5760901906	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3010745998, ss5209242587	NC_000013.10:26937464::AAAAAAAAAAA… NC_000013.10:26937464::AAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694956226, ss5487569556, ss5760901904	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss82302002, ss95615065	NT_024524.14:7917478::AAAAAAAAAAAA… NT_024524.14:7917478::AAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3010746001	NC_000013.10:26937464::AAAAAAAAAAA… NC_000013.10:26937464::AAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5760901905	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3010745999, ss5209242589	NC_000013.10:26937464::AAAAAAAAAAA… NC_000013.10:26937464::AAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5760901907	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5639637788	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4262971626	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4262971627	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3188357209	NC_000013.11:26363327::AAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
ss3188357211	NC_000013.11:26363327::AAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA
ss3188357212	NC_000013.11:26363327::AAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
ss3188357213	NC_000013.11:26363327::AAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
ss3188357215	NC_000013.11:26363327::AAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
ss3188357223	NC_000013.11:26363327::AAAAAAAAAAA… NC_000013.11:26363327::AAAAAAAAAAAAAAAAAAA	NC_000013.11:26363327:AAAAAAAAAAAA… NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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

No publications for rs71188725

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

rs71188725