Name: rs57194999
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.

rs57194999

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:128650527-128650548 (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(AT)₅ / del(AT)₄ / del(AT)₃ / d…
del(AT)₅ / del(AT)₄ / del(AT)₃ / delATAT / delAT / dupAT / dupATAT / dup(AT)₃ / dup(AT)₄ / dup(AT)₅ / dup(AT)₆ / dup(AT)₇ / dup(AT)₈ / dup(AT)₉ / dup(AT)₁₀ / dup(AT)₁₁ / ins(AT)₁₂ / ins(AT)₁₃ / ins(AT)₁₄ / ins(AT)₁₅ / ins(AT)₁₆ / ins(AT)₁₈ / ins(AT)₂₀ / ins(AT)₂₁ / insATT(AT)₁₁ / insATT(AT)₁₁AA(TA)₁₀T / insATT(AT)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: del(AT)₅=0.0000 (0/3758, ALFA)
del(AT)₄=0.0000 (0/3758, ALFA)
del(AT)₃=0.0000 (0/3758, ALFA) (+ 16 more)
delATAT=0.0000 (0/3758, ALFA)
delAT=0.0000 (0/3758, ALFA)
dupAT=0.0000 (0/3758, ALFA)
dupATAT=0.0000 (0/3758, ALFA)
dup(AT)₃=0.0000 (0/3758, ALFA)
dup(AT)₄=0.0000 (0/3758, ALFA)
dup(AT)₅=0.0000 (0/3758, ALFA)
dup(AT)₆=0.0000 (0/3758, ALFA)
dup(AT)₇=0.0000 (0/3758, ALFA)
dup(AT)₈=0.0000 (0/3758, ALFA)
dup(AT)₉=0.0000 (0/3758, ALFA)
dup(AT)₁₀=0.0000 (0/3758, ALFA)
dup(AT)₁₁=0.0000 (0/3758, ALFA)
ins(AT)₁₂=0.0000 (0/3758, ALFA)
ins(AT)₁₃=0.0000 (0/3758, ALFA)
insATT(AT)₁₁=0.0000 (0/3758, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DYNC2I2 : 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	HWEP
Total	Global	3758	ATATATATATATATATATATAT=1.0000	ATATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.0000	1.0	N/A
European	Sub	862	ATATATATATATATATATATAT=1.000	ATATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.000	1.0	N/A
African	Sub	1928	ATATATATATATATATATATAT=1.0000	ATATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.0000	1.0	N/A
African Others	Sub	68	ATATATATATATATATATATAT=1.00	ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.00	1.0	N/A
African American	Sub	1860	ATATATATATATATATATATAT=1.0000	ATATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.0000	1.0	N/A
Asian	Sub	58	ATATATATATATATATATATAT=1.00	ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.00	1.0	N/A
East Asian	Sub	46	ATATATATATATATATATATAT=1.00	ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.00	1.0	N/A
Other Asian	Sub	12	ATATATATATATATATATATAT=1.00	ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.00	1.0	N/A
Latin American 1	Sub	108	ATATATATATATATATATATAT=1.000	ATATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.000	1.0	N/A
Latin American 2	Sub	538	ATATATATATATATATATATAT=1.000	ATATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.000	1.0	N/A
South Asian	Sub	20	ATATATATATATATATATATAT=1.00	ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.00	1.0	N/A
Other	Sub	244	ATATATATATATATATATATAT=1.000	ATATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATTATATATATATATATATATATAT=0.000	1.0	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	3758	(AT)₁₁=1.0000	del(AT)₅=0.0000, del(AT)₄=0.0000, del(AT)₃=0.0000, delATAT=0.0000, delAT=0.0000, dupAT=0.0000, dupATAT=0.0000, dup(AT)₃=0.0000, dup(AT)₄=0.0000, dup(AT)₅=0.0000, dup(AT)₆=0.0000, dup(AT)₇=0.0000, dup(AT)₈=0.0000, dup(AT)₉=0.0000, dup(AT)₁₀=0.0000, dup(AT)₁₁=0.0000, ins(AT)₁₂=0.0000, ins(AT)₁₃=0.0000, insATT(AT)₁₁=0.0000
Allele Frequency Aggregator	African	Sub	1928	(AT)₁₁=1.0000	del(AT)₅=0.0000, del(AT)₄=0.0000, del(AT)₃=0.0000, delATAT=0.0000, delAT=0.0000, dupAT=0.0000, dupATAT=0.0000, dup(AT)₃=0.0000, dup(AT)₄=0.0000, dup(AT)₅=0.0000, dup(AT)₆=0.0000, dup(AT)₇=0.0000, dup(AT)₈=0.0000, dup(AT)₉=0.0000, dup(AT)₁₀=0.0000, dup(AT)₁₁=0.0000, ins(AT)₁₂=0.0000, ins(AT)₁₃=0.0000, insATT(AT)₁₁=0.0000
Allele Frequency Aggregator	European	Sub	862	(AT)₁₁=1.000	del(AT)₅=0.000, del(AT)₄=0.000, del(AT)₃=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000, dup(AT)₄=0.000, dup(AT)₅=0.000, dup(AT)₆=0.000, dup(AT)₇=0.000, dup(AT)₈=0.000, dup(AT)₉=0.000, dup(AT)₁₀=0.000, dup(AT)₁₁=0.000, ins(AT)₁₂=0.000, ins(AT)₁₃=0.000, insATT(AT)₁₁=0.000
Allele Frequency Aggregator	Latin American 2	Sub	538	(AT)₁₁=1.000	del(AT)₅=0.000, del(AT)₄=0.000, del(AT)₃=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000, dup(AT)₄=0.000, dup(AT)₅=0.000, dup(AT)₆=0.000, dup(AT)₇=0.000, dup(AT)₈=0.000, dup(AT)₉=0.000, dup(AT)₁₀=0.000, dup(AT)₁₁=0.000, ins(AT)₁₂=0.000, ins(AT)₁₃=0.000, insATT(AT)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	244	(AT)₁₁=1.000	del(AT)₅=0.000, del(AT)₄=0.000, del(AT)₃=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000, dup(AT)₄=0.000, dup(AT)₅=0.000, dup(AT)₆=0.000, dup(AT)₇=0.000, dup(AT)₈=0.000, dup(AT)₉=0.000, dup(AT)₁₀=0.000, dup(AT)₁₁=0.000, ins(AT)₁₂=0.000, ins(AT)₁₃=0.000, insATT(AT)₁₁=0.000
Allele Frequency Aggregator	Latin American 1	Sub	108	(AT)₁₁=1.000	del(AT)₅=0.000, del(AT)₄=0.000, del(AT)₃=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000, dup(AT)₄=0.000, dup(AT)₅=0.000, dup(AT)₆=0.000, dup(AT)₇=0.000, dup(AT)₈=0.000, dup(AT)₉=0.000, dup(AT)₁₀=0.000, dup(AT)₁₁=0.000, ins(AT)₁₂=0.000, ins(AT)₁₃=0.000, insATT(AT)₁₁=0.000
Allele Frequency Aggregator	Asian	Sub	58	(AT)₁₁=1.00	del(AT)₅=0.00, del(AT)₄=0.00, del(AT)₃=0.00, delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00, dup(AT)₃=0.00, dup(AT)₄=0.00, dup(AT)₅=0.00, dup(AT)₆=0.00, dup(AT)₇=0.00, dup(AT)₈=0.00, dup(AT)₉=0.00, dup(AT)₁₀=0.00, dup(AT)₁₁=0.00, ins(AT)₁₂=0.00, ins(AT)₁₃=0.00, insATT(AT)₁₁=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(AT)₁₁=1.00	del(AT)₅=0.00, del(AT)₄=0.00, del(AT)₃=0.00, delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00, dup(AT)₃=0.00, dup(AT)₄=0.00, dup(AT)₅=0.00, dup(AT)₆=0.00, dup(AT)₇=0.00, dup(AT)₈=0.00, dup(AT)₉=0.00, dup(AT)₁₀=0.00, dup(AT)₁₁=0.00, ins(AT)₁₂=0.00, ins(AT)₁₃=0.00, insATT(AT)₁₁=0.00

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 9	NC_000009.12:g.128650527AT[6]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[7]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[8]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[9]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[10]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[12]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[13]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[14]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[15]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[16]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[17]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[18]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[19]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[20]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[21]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[22]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[23]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[24]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[25]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[26]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[27]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[29]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[31]
GRCh38.p14 chr 9	NC_000009.12:g.128650527AT[32]
GRCh38.p14 chr 9	NC_000009.12:g.128650527_128650548AT[12]TA[11]T[1]
GRCh38.p14 chr 9	NC_000009.12:g.128650527_128650548AT[12]TA[12]AT[11]
GRCh38.p14 chr 9	NC_000009.12:g.128650527_128650548AT[12]TA[18]T[1]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[6]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[7]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[8]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[9]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[10]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[12]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[13]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[14]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[15]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[16]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[17]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[18]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[19]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[20]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[21]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[22]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[23]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[24]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[25]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[26]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[27]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[29]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[31]
GRCh37.p13 chr 9	NC_000009.11:g.131412806AT[32]
GRCh37.p13 chr 9	NC_000009.11:g.131412806_131412827AT[12]TA[11]T[1]
GRCh37.p13 chr 9	NC_000009.11:g.131412806_131412827AT[12]TA[12]AT[11]
GRCh37.p13 chr 9	NC_000009.11:g.131412806_131412827AT[12]TA[18]T[1]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[6]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[7]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[8]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[9]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[10]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[12]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[13]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[14]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[15]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[16]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[17]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[18]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[19]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[20]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[21]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[22]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[23]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[24]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[25]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[26]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[27]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[29]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[31]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303AT[32]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303_11324ATATATATATATATATATATATA[2]T[1]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303_11324AT[11]TA[12]AT[12]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303_11324AT[18]AATATATATATATATATATATATAT[1]

Gene: DYNC2I2, dynein 2 intermediate chain 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DYNC2I2 transcript	NM_052844.4:c.186+5993AT[… NM_052844.4:c.186+5993AT[6]	N/A	Intron Variant
DYNC2I2 transcript variant X2	XM_011519179.3:c.186+5993… XM_011519179.3:c.186+5993AT[6]	N/A	Intron Variant
DYNC2I2 transcript variant X1	XM_047424057.1:c.186+5993… XM_047424057.1:c.186+5993AT[6]	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(AT)₁₁=	del(AT)₅	del(AT)₄	del(AT)₃	delATAT	delAT	dupAT	dupATAT	dup(AT)₃	dup(AT)₄	dup(AT)₅	dup(AT)₆	dup(AT)₇	dup(AT)₈	dup(AT)₉	dup(AT)₁₀	dup(AT)₁₁	ins(AT)₁₂	ins(AT)₁₃	ins(AT)₁₄	ins(AT)₁₅	ins(AT)₁₆	ins(AT)₁₈	ins(AT)₂₀	ins(AT)₂₁	insATT(AT)₁₁	insATT(AT)₁₁AA(TA)₁₀T	insATT(AT)₁₈
GRCh38.p14 chr 9	NC_000009.12:g.128650527_128650548=	NC_000009.12:g.128650527AT[6]	NC_000009.12:g.128650527AT[7]	NC_000009.12:g.128650527AT[8]	NC_000009.12:g.128650527AT[9]	NC_000009.12:g.128650527AT[10]	NC_000009.12:g.128650527AT[12]	NC_000009.12:g.128650527AT[13]	NC_000009.12:g.128650527AT[14]	NC_000009.12:g.128650527AT[15]	NC_000009.12:g.128650527AT[16]	NC_000009.12:g.128650527AT[17]	NC_000009.12:g.128650527AT[18]	NC_000009.12:g.128650527AT[19]	NC_000009.12:g.128650527AT[20]	NC_000009.12:g.128650527AT[21]	NC_000009.12:g.128650527AT[22]	NC_000009.12:g.128650527AT[23]	NC_000009.12:g.128650527AT[24]	NC_000009.12:g.128650527AT[25]	NC_000009.12:g.128650527AT[26]	NC_000009.12:g.128650527AT[27]	NC_000009.12:g.128650527AT[29]	NC_000009.12:g.128650527AT[31]	NC_000009.12:g.128650527AT[32]	NC_000009.12:g.128650527_128650548AT[12]TA[11]T[1]	NC_000009.12:g.128650527_128650548AT[12]TA[12]AT[11]	NC_000009.12:g.128650527_128650548AT[12]TA[18]T[1]
GRCh37.p13 chr 9	NC_000009.11:g.131412806_131412827=	NC_000009.11:g.131412806AT[6]	NC_000009.11:g.131412806AT[7]	NC_000009.11:g.131412806AT[8]	NC_000009.11:g.131412806AT[9]	NC_000009.11:g.131412806AT[10]	NC_000009.11:g.131412806AT[12]	NC_000009.11:g.131412806AT[13]	NC_000009.11:g.131412806AT[14]	NC_000009.11:g.131412806AT[15]	NC_000009.11:g.131412806AT[16]	NC_000009.11:g.131412806AT[17]	NC_000009.11:g.131412806AT[18]	NC_000009.11:g.131412806AT[19]	NC_000009.11:g.131412806AT[20]	NC_000009.11:g.131412806AT[21]	NC_000009.11:g.131412806AT[22]	NC_000009.11:g.131412806AT[23]	NC_000009.11:g.131412806AT[24]	NC_000009.11:g.131412806AT[25]	NC_000009.11:g.131412806AT[26]	NC_000009.11:g.131412806AT[27]	NC_000009.11:g.131412806AT[29]	NC_000009.11:g.131412806AT[31]	NC_000009.11:g.131412806AT[32]	NC_000009.11:g.131412806_131412827AT[12]TA[11]T[1]	NC_000009.11:g.131412806_131412827AT[12]TA[12]AT[11]	NC_000009.11:g.131412806_131412827AT[12]TA[18]T[1]
DYNC2I2 RefSeqGene	NG_034056.1:g.11303_11324=	NG_034056.1:g.11303AT[6]	NG_034056.1:g.11303AT[7]	NG_034056.1:g.11303AT[8]	NG_034056.1:g.11303AT[9]	NG_034056.1:g.11303AT[10]	NG_034056.1:g.11303AT[12]	NG_034056.1:g.11303AT[13]	NG_034056.1:g.11303AT[14]	NG_034056.1:g.11303AT[15]	NG_034056.1:g.11303AT[16]	NG_034056.1:g.11303AT[17]	NG_034056.1:g.11303AT[18]	NG_034056.1:g.11303AT[19]	NG_034056.1:g.11303AT[20]	NG_034056.1:g.11303AT[21]	NG_034056.1:g.11303AT[22]	NG_034056.1:g.11303AT[23]	NG_034056.1:g.11303AT[24]	NG_034056.1:g.11303AT[25]	NG_034056.1:g.11303AT[26]	NG_034056.1:g.11303AT[27]	NG_034056.1:g.11303AT[29]	NG_034056.1:g.11303AT[31]	NG_034056.1:g.11303AT[32]	NG_034056.1:g.11303_11324ATATATATATATATATATATATA[2]T[1]	NG_034056.1:g.11303_11324AT[11]TA[12]AT[12]	NG_034056.1:g.11303_11324AT[18]AATATATATATATATATATATATAT[1]
DYNC2I2 transcript	NM_052844.3:c.186+6014=	NM_052844.3:c.186+5993AT[6]	NM_052844.3:c.186+5993AT[7]	NM_052844.3:c.186+5993AT[8]	NM_052844.3:c.186+5993AT[9]	NM_052844.3:c.186+5993AT[10]	NM_052844.3:c.186+5993AT[12]	NM_052844.3:c.186+5993AT[13]	NM_052844.3:c.186+5993AT[14]	NM_052844.3:c.186+5993AT[15]	NM_052844.3:c.186+5993AT[16]	NM_052844.3:c.186+5993AT[17]	NM_052844.3:c.186+5993AT[18]	NM_052844.3:c.186+5993AT[19]	NM_052844.3:c.186+5993AT[20]	NM_052844.3:c.186+5993AT[21]	NM_052844.3:c.186+5993AT[22]	NM_052844.3:c.186+5993AT[23]	NM_052844.3:c.186+5993AT[24]	NM_052844.3:c.186+5993AT[25]	NM_052844.3:c.186+5993AT[26]	NM_052844.3:c.186+5993AT[27]	NM_052844.3:c.186+5993AT[29]	NM_052844.3:c.186+5993AT[31]	NM_052844.3:c.186+5993AT[32]	NM_052844.3:c.186+6014_186+6015insATATATATATATATATATATATAAT	NM_052844.3:c.186+6014_186+6015insATATATATATATATATATATATTATATATATATATATATATATATAAT	NM_052844.3:c.186+6014_186+6015insATATATATATATATATATATATATATATATATATATAAT
DYNC2I2 transcript	NM_052844.4:c.186+6014=	NM_052844.4:c.186+5993AT[6]	NM_052844.4:c.186+5993AT[7]	NM_052844.4:c.186+5993AT[8]	NM_052844.4:c.186+5993AT[9]	NM_052844.4:c.186+5993AT[10]	NM_052844.4:c.186+5993AT[12]	NM_052844.4:c.186+5993AT[13]	NM_052844.4:c.186+5993AT[14]	NM_052844.4:c.186+5993AT[15]	NM_052844.4:c.186+5993AT[16]	NM_052844.4:c.186+5993AT[17]	NM_052844.4:c.186+5993AT[18]	NM_052844.4:c.186+5993AT[19]	NM_052844.4:c.186+5993AT[20]	NM_052844.4:c.186+5993AT[21]	NM_052844.4:c.186+5993AT[22]	NM_052844.4:c.186+5993AT[23]	NM_052844.4:c.186+5993AT[24]	NM_052844.4:c.186+5993AT[25]	NM_052844.4:c.186+5993AT[26]	NM_052844.4:c.186+5993AT[27]	NM_052844.4:c.186+5993AT[29]	NM_052844.4:c.186+5993AT[31]	NM_052844.4:c.186+5993AT[32]	NM_052844.4:c.186+6014_186+6015insATATATATATATATATATATATAAT	NM_052844.4:c.186+6014_186+6015insATATATATATATATATATATATTATATATATATATATATATATATAAT	NM_052844.4:c.186+6014_186+6015insATATATATATATATATATATATATATATATATATATAAT
DYNC2I2 transcript variant X2	XM_011519179.3:c.186+6014=	XM_011519179.3:c.186+5993AT[6]	XM_011519179.3:c.186+5993AT[7]	XM_011519179.3:c.186+5993AT[8]	XM_011519179.3:c.186+5993AT[9]	XM_011519179.3:c.186+5993AT[10]	XM_011519179.3:c.186+5993AT[12]	XM_011519179.3:c.186+5993AT[13]	XM_011519179.3:c.186+5993AT[14]	XM_011519179.3:c.186+5993AT[15]	XM_011519179.3:c.186+5993AT[16]	XM_011519179.3:c.186+5993AT[17]	XM_011519179.3:c.186+5993AT[18]	XM_011519179.3:c.186+5993AT[19]	XM_011519179.3:c.186+5993AT[20]	XM_011519179.3:c.186+5993AT[21]	XM_011519179.3:c.186+5993AT[22]	XM_011519179.3:c.186+5993AT[23]	XM_011519179.3:c.186+5993AT[24]	XM_011519179.3:c.186+5993AT[25]	XM_011519179.3:c.186+5993AT[26]	XM_011519179.3:c.186+5993AT[27]	XM_011519179.3:c.186+5993AT[29]	XM_011519179.3:c.186+5993AT[31]	XM_011519179.3:c.186+5993AT[32]	XM_011519179.3:c.186+6014_186+6015insATATATATATATATATATATATAAT	XM_011519179.3:c.186+6014_186+6015insATATATATATATATATATATATTATATATATATATATATATATATAAT	XM_011519179.3:c.186+6014_186+6015insATATATATATATATATATATATATATATATATATATAAT
DYNC2I2 transcript variant X1	XM_047424057.1:c.186+6014=	XM_047424057.1:c.186+5993AT[6]	XM_047424057.1:c.186+5993AT[7]	XM_047424057.1:c.186+5993AT[8]	XM_047424057.1:c.186+5993AT[9]	XM_047424057.1:c.186+5993AT[10]	XM_047424057.1:c.186+5993AT[12]	XM_047424057.1:c.186+5993AT[13]	XM_047424057.1:c.186+5993AT[14]	XM_047424057.1:c.186+5993AT[15]	XM_047424057.1:c.186+5993AT[16]	XM_047424057.1:c.186+5993AT[17]	XM_047424057.1:c.186+5993AT[18]	XM_047424057.1:c.186+5993AT[19]	XM_047424057.1:c.186+5993AT[20]	XM_047424057.1:c.186+5993AT[21]	XM_047424057.1:c.186+5993AT[22]	XM_047424057.1:c.186+5993AT[23]	XM_047424057.1:c.186+5993AT[24]	XM_047424057.1:c.186+5993AT[25]	XM_047424057.1:c.186+5993AT[26]	XM_047424057.1:c.186+5993AT[27]	XM_047424057.1:c.186+5993AT[29]	XM_047424057.1:c.186+5993AT[31]	XM_047424057.1:c.186+5993AT[32]	XM_047424057.1:c.186+6014_186+6015insATATATATATATATATATATATAAT	XM_047424057.1:c.186+6014_186+6015insATATATATATATATATATATATTATATATATATATATATATATATAAT	XM_047424057.1:c.186+6014_186+6015insATATATATATATATATATATATATATATATATATATAAT

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

67 SubSNP, 43 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83422777	Dec 14, 2007 (129)
2	BUSHMAN	ss194043584	Jul 04, 2010 (137)
3	GMI	ss288986708	May 04, 2012 (137)
4	GMI	ss288986709	May 04, 2012 (137)
5	LUNTER	ss551983464	Apr 25, 2013 (138)
6	LUNTER	ss552218534	Apr 25, 2013 (138)
7	LUNTER	ss553393653	Apr 25, 2013 (138)
8	SSMP	ss663901930	Apr 01, 2015 (144)
9	DDI	ss1536635776	Apr 01, 2015 (144)
10	SWEGEN	ss3005647459	Nov 08, 2017 (151)
11	MCHAISSO	ss3066270803	Nov 08, 2017 (151)
12	EVA_DECODE	ss3724820655	Jul 13, 2019 (153)
13	EVA_DECODE	ss3724820656	Jul 13, 2019 (153)
14	EVA_DECODE	ss3724820657	Jul 13, 2019 (153)
15	EVA_DECODE	ss3724820658	Jul 13, 2019 (153)
16	EVA_DECODE	ss3724820659	Jul 13, 2019 (153)
17	PACBIO	ss3786532240	Jul 13, 2019 (153)
18	PACBIO	ss3791729480	Jul 13, 2019 (153)
19	PACBIO	ss3796611046	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3812896225	Jul 13, 2019 (153)
21	EVA	ss3831876511	Apr 26, 2020 (154)
22	KOGIC	ss3966823890	Apr 26, 2020 (154)
23	KOGIC	ss3966823891	Apr 26, 2020 (154)
24	KOGIC	ss3966823892	Apr 26, 2020 (154)
25	KOGIC	ss3966823893	Apr 26, 2020 (154)
26	KOGIC	ss3966823894	Apr 26, 2020 (154)
27	GNOMAD	ss4210046593	Apr 26, 2021 (155)
28	GNOMAD	ss4210046594	Apr 26, 2021 (155)
29	GNOMAD	ss4210046595	Apr 26, 2021 (155)
30	GNOMAD	ss4210046596	Apr 26, 2021 (155)
31	GNOMAD	ss4210046597	Apr 26, 2021 (155)
32	GNOMAD	ss4210046598	Apr 26, 2021 (155)
33	GNOMAD	ss4210046599	Apr 26, 2021 (155)
34	GNOMAD	ss4210046600	Apr 26, 2021 (155)
35	GNOMAD	ss4210046601	Apr 26, 2021 (155)
36	GNOMAD	ss4210046602	Apr 26, 2021 (155)
37	GNOMAD	ss4210046603	Apr 26, 2021 (155)
38	GNOMAD	ss4210046604	Apr 26, 2021 (155)
39	GNOMAD	ss4210046605	Apr 26, 2021 (155)
40	GNOMAD	ss4210046606	Apr 26, 2021 (155)
41	GNOMAD	ss4210046607	Apr 26, 2021 (155)
42	GNOMAD	ss4210046608	Apr 26, 2021 (155)
43	GNOMAD	ss4210046609	Apr 26, 2021 (155)
44	GNOMAD	ss4210046610	Apr 26, 2021 (155)
45	GNOMAD	ss4210046611	Apr 26, 2021 (155)
46	GNOMAD	ss4210046612	Apr 26, 2021 (155)
47	GNOMAD	ss4210046613	Apr 26, 2021 (155)
48	GNOMAD	ss4210046616	Apr 26, 2021 (155)
49	GNOMAD	ss4210046617	Apr 26, 2021 (155)
50	GNOMAD	ss4210046618	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5195461208	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5195461209	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5195461210	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5195461211	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5195461212	Apr 26, 2021 (155)
56	HUGCELL_USP	ss5478157246	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5478157247	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5478157248	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5478157249	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5740042222	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5740042223	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5740042224	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5740042225	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5740042226	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5740042227	Oct 16, 2022 (156)
66	EVA	ss5829795862	Oct 16, 2022 (156)
67	EVA	ss5829795863	Oct 16, 2022 (156)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338685590 (NC_000009.12:128650526::AT 667/37618) Row 338685591 (NC_000009.12:128650526::ATAT 110/37666) Row 338685592 (NC_000009.12:128650526::ATATAT 6/37670)...	-	Apr 26, 2021 (155)
92	Korean Genome Project Submission ignored due to conflicting rows: Row 23201891 (NC_000009.12:128650528:ATAT: 469/1304) Row 23201892 (NC_000009.12:128650530:AT: 109/1304) Row 23201893 (NC_000009.12:128650532::AT 26/1304)...	-	Apr 26, 2020 (154)
93	Korean Genome Project Submission ignored due to conflicting rows: Row 23201891 (NC_000009.12:128650528:ATAT: 469/1304) Row 23201892 (NC_000009.12:128650530:AT: 109/1304) Row 23201893 (NC_000009.12:128650532::AT 26/1304)...	-	Apr 26, 2020 (154)
94	Korean Genome Project Submission ignored due to conflicting rows: Row 23201891 (NC_000009.12:128650528:ATAT: 469/1304) Row 23201892 (NC_000009.12:128650530:AT: 109/1304) Row 23201893 (NC_000009.12:128650532::AT 26/1304)...	-	Apr 26, 2020 (154)
95	Korean Genome Project Submission ignored due to conflicting rows: Row 23201891 (NC_000009.12:128650528:ATAT: 469/1304) Row 23201892 (NC_000009.12:128650530:AT: 109/1304) Row 23201893 (NC_000009.12:128650532::AT 26/1304)...	-	Apr 26, 2020 (154)
96	Korean Genome Project Submission ignored due to conflicting rows: Row 23201891 (NC_000009.12:128650528:ATAT: 469/1304) Row 23201892 (NC_000009.12:128650530:AT: 109/1304) Row 23201893 (NC_000009.12:128650532::AT 26/1304)...	-	Apr 26, 2020 (154)
97	8.3KJPN Submission ignored due to conflicting rows: Row 53430515 (NC_000009.11:131412805:ATAT: 6882/13046) Row 53430516 (NC_000009.11:131412805:AT: 53/13046) Row 53430517 (NC_000009.11:131412805::AT 29/13046)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 53430515 (NC_000009.11:131412805:ATAT: 6882/13046) Row 53430516 (NC_000009.11:131412805:AT: 53/13046) Row 53430517 (NC_000009.11:131412805::AT 29/13046)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 53430515 (NC_000009.11:131412805:ATAT: 6882/13046) Row 53430516 (NC_000009.11:131412805:AT: 53/13046) Row 53430517 (NC_000009.11:131412805::AT 29/13046)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 53430515 (NC_000009.11:131412805:ATAT: 6882/13046) Row 53430516 (NC_000009.11:131412805:AT: 53/13046) Row 53430517 (NC_000009.11:131412805::AT 29/13046)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 53430515 (NC_000009.11:131412805:ATAT: 6882/13046) Row 53430516 (NC_000009.11:131412805:AT: 53/13046) Row 53430517 (NC_000009.11:131412805::AT 29/13046)...	-	Apr 26, 2021 (155)
102	14KJPN Submission ignored due to conflicting rows: Row 73879326 (NC_000009.12:128650526:ATAT: 11631/22086) Row 73879327 (NC_000009.12:128650526::AT 42/22086) Row 73879328 (NC_000009.12:128650526:AT: 88/22086)...	-	Oct 16, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 73879326 (NC_000009.12:128650526:ATAT: 11631/22086) Row 73879327 (NC_000009.12:128650526::AT 42/22086) Row 73879328 (NC_000009.12:128650526:AT: 88/22086)...	-	Oct 16, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 73879326 (NC_000009.12:128650526:ATAT: 11631/22086) Row 73879327 (NC_000009.12:128650526::AT 42/22086) Row 73879328 (NC_000009.12:128650526:AT: 88/22086)...	-	Oct 16, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 73879326 (NC_000009.12:128650526:ATAT: 11631/22086) Row 73879327 (NC_000009.12:128650526::AT 42/22086) Row 73879328 (NC_000009.12:128650526:AT: 88/22086)...	-	Oct 16, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 73879326 (NC_000009.12:128650526:ATAT: 11631/22086) Row 73879327 (NC_000009.12:128650526::AT 42/22086) Row 73879328 (NC_000009.12:128650526:AT: 88/22086)...	-	Oct 16, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 73879326 (NC_000009.12:128650526:ATAT: 11631/22086) Row 73879327 (NC_000009.12:128650526::AT 42/22086) Row 73879328 (NC_000009.12:128650526:AT: 88/22086)...	-	Oct 16, 2022 (156)
108	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 5913455 (NC_000009.11:131412805::AT 2/103) Row 5913456 (NC_000009.11:131412805:ATAT: 49/150)	-	Jul 13, 2019 (153)
109	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 5913455 (NC_000009.11:131412805::AT 2/103) Row 5913456 (NC_000009.11:131412805:ATAT: 49/150)	-	Jul 13, 2019 (153)
110	ALFA	NC_000009.12 - 128650527	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)
rs72122223	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATAT	(self)
ss3724820659	NC_000009.12:128650526:ATATATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATAT	(self)
ss3966823893, ss4210046618, ss5740042226	NC_000009.12:128650526:ATATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATAT	(self)
ss3724820658	NC_000009.12:128650528:ATATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATAT	(self)
ss288986708, ss551983464, ss552218534, ss553393653	NC_000009.10:130452626:ATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATAT	(self)
ss663901930, ss1536635776, ss3005647459, ss3786532240, ss3791729480, ss3796611046, ss3831876511, ss5195461208, ss5829795862	NC_000009.11:131412805:ATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATAT	(self)
ss3812896225, ss4210046617, ss5478157247, ss5740042222	NC_000009.12:128650526:ATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATAT	(self)
ss3966823890	NC_000009.12:128650528:ATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATAT	(self)
ss3724820657	NC_000009.12:128650530:ATAT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATAT	(self)
ss83422777	NC_000009.9:128492379:AT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
ss5195461209, ss5829795863	NC_000009.11:131412805:AT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
ss4210046616, ss5478157246, ss5740042224	NC_000009.12:128650526:AT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
ss3966823891	NC_000009.12:128650530:AT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
ss3724820656	NC_000009.12:128650532:AT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
ss194043584	NT_008470.20:60429974:AT:	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
ss288986709	NC_000009.10:130452648::AT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
ss5195461210	NC_000009.11:131412805::AT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
ss4210046593, ss5478157248, ss5740042223	NC_000009.12:128650526::AT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
ss3966823892	NC_000009.12:128650532::AT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
ss3724820655	NC_000009.12:128650534::AT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
ss5195461211	NC_000009.11:131412805::ATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATAT	(self)
ss4210046594, ss5478157249, ss5740042225	NC_000009.12:128650526::ATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATAT	(self)
ss3966823894	NC_000009.12:128650532::ATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATAT	(self)
ss5195461212	NC_000009.11:131412805::ATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATAT	(self)
ss4210046595, ss5740042227	NC_000009.12:128650526::ATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATAT	(self)
ss4210046596	NC_000009.12:128650526::ATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT	(self)
ss4210046597	NC_000009.12:128650526::ATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT	(self)
ss4210046598	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT	(self)
ss4210046599	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT	(self)
ss4210046600	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046601	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046602	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046603	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046604	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss3066270803	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046605	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046606	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046607	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046608	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046609	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046610	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4210046611	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATTATATATATATATATATATATAT	(self)
5806589584	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATTATATATATATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATTATATATATATATATATATATAT	(self)
ss4210046613	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATTATATATATATATATATATATATA	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATTATATATATATATATATATATATAATATATATATATATATATATAT	(self)
ss4210046612	NC_000009.12:128650526::ATATATATAT… NC_000009.12:128650526::ATATATATATATATATATATATATTATATATATATATAT	NC_000009.12:128650526:ATATATATATA… NC_000009.12:128650526:ATATATATATATATATATATAT:ATATATATATATATATATATATATTATATATATATATATATATATATATATATATATATAT	(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 rs57194999

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
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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

rs57194999