Name: rs773774279
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.

rs773774279

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:129344629-129344650 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₆ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₆ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₂ / dup(A)₁₃ / dup(A)₁₄ / dup(A)₁₅ / dup(A)₁₆ / dup(A)₁₇ / dup(A)₁₈ / dup(A)₁₉ / dup(A)₂₀ / dup(A)₂₁ / ins(A)₂₃ / ins(A)₂₄ / ins(A)₂₆ / ins(A)₃₀
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.000015 (4/264690, TOPMED)
del(A)₁₆=0.0000 (0/8596, ALFA)
del(A)₁₂=0.0000 (0/8596, ALFA) (+ 17 more)
del(A)₁₁=0.0000 (0/8596, ALFA)
del(A)₁₀=0.0000 (0/8596, ALFA)
del(A)₈=0.0000 (0/8596, ALFA)
del(A)₇=0.0000 (0/8596, ALFA)
del(A)₆=0.0000 (0/8596, ALFA)
del(A)₅=0.0000 (0/8596, ALFA)
del(A)₄=0.0000 (0/8596, ALFA)
delAAA=0.0000 (0/8596, ALFA)
delAA=0.0000 (0/8596, ALFA)
delA=0.0000 (0/8596, ALFA)
dupA=0.0000 (0/8596, ALFA)
dupAA=0.0000 (0/8596, ALFA)
dupAAA=0.0000 (0/8596, ALFA)
dup(A)₄=0.0000 (0/8596, ALFA)
dup(A)₅=0.0000 (0/8596, ALFA)
dup(A)₆=0.0000 (0/8596, ALFA)
dup(A)₇=0.0000 (0/8596, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01503 : 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	8596	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	6866	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	920	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	36	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	884	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	54	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	42	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	90	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	370	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	54	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	242	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₂₂=0.999985	del(A)₁₁=0.000015
Allele Frequency Aggregator	Total	Global	8596	(A)₂₂=1.0000	del(A)₁₆=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, 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
Allele Frequency Aggregator	European	Sub	6866	(A)₂₂=1.0000	del(A)₁₆=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, 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
Allele Frequency Aggregator	African	Sub	920	(A)₂₂=1.000	del(A)₁₆=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	370	(A)₂₂=1.000	del(A)₁₆=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Other	Sub	242	(A)₂₂=1.000	del(A)₁₆=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	90	(A)₂₂=1.00	del(A)₁₆=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	54	(A)₂₂=1.00	del(A)₁₆=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Asian	Sub	54	(A)₂₂=1.00	del(A)₁₆=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=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.129344635_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344638_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344639_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344640_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344641_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344643_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344644_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344645_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344646_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344647_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344648_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344649_129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344650del
GRCh38.p14 chr 9	NC_000009.12:g.129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344649_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344648_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344647_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344646_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344645_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344644_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344643_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344642_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344641_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344640_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344639_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344638_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344637_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344636_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344635_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344634_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344633_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344632_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344631_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344630_129344650dup
GRCh38.p14 chr 9	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 9	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 9	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 9	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 9	NC_000009.11:g.132106914_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106917_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106918_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106919_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106920_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106922_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106923_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106924_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106925_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106926_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106927_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106928_132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106929del
GRCh37.p13 chr 9	NC_000009.11:g.132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106928_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106927_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106926_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106925_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106924_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106923_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106922_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106921_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106920_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106919_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106918_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106917_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106916_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106915_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106914_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106913_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106912_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106911_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106910_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106909_132106929dup
GRCh37.p13 chr 9	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 9	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 9	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 9	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: LINC01503, long intergenic non-protein coding RNA 1503 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01503 transcript variant 1	NR_120685.1:n.	N/A	Intron Variant
LINC01503 transcript variant 2	NR_120686.1:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(A)₂₂=	del(A)₁₆	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₂	dup(A)₁₃	dup(A)₁₄	dup(A)₁₅	dup(A)₁₆	dup(A)₁₇	dup(A)₁₈	dup(A)₁₉	dup(A)₂₀	dup(A)₂₁	ins(A)₂₃	ins(A)₂₄	ins(A)₂₆	ins(A)₃₀
GRCh38.p14 chr 9	NC_000009.12:g.129344629_129344650=	NC_000009.12:g.129344635_129344650del	NC_000009.12:g.129344638_129344650del	NC_000009.12:g.129344639_129344650del	NC_000009.12:g.129344640_129344650del	NC_000009.12:g.129344641_129344650del	NC_000009.12:g.129344643_129344650del	NC_000009.12:g.129344644_129344650del	NC_000009.12:g.129344645_129344650del	NC_000009.12:g.129344646_129344650del	NC_000009.12:g.129344647_129344650del	NC_000009.12:g.129344648_129344650del	NC_000009.12:g.129344649_129344650del	NC_000009.12:g.129344650del	NC_000009.12:g.129344650dup	NC_000009.12:g.129344649_129344650dup	NC_000009.12:g.129344648_129344650dup	NC_000009.12:g.129344647_129344650dup	NC_000009.12:g.129344646_129344650dup	NC_000009.12:g.129344645_129344650dup	NC_000009.12:g.129344644_129344650dup	NC_000009.12:g.129344643_129344650dup	NC_000009.12:g.129344642_129344650dup	NC_000009.12:g.129344641_129344650dup	NC_000009.12:g.129344640_129344650dup	NC_000009.12:g.129344639_129344650dup	NC_000009.12:g.129344638_129344650dup	NC_000009.12:g.129344637_129344650dup	NC_000009.12:g.129344636_129344650dup	NC_000009.12:g.129344635_129344650dup	NC_000009.12:g.129344634_129344650dup	NC_000009.12:g.129344633_129344650dup	NC_000009.12:g.129344632_129344650dup	NC_000009.12:g.129344631_129344650dup	NC_000009.12:g.129344630_129344650dup	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:g.129344650_129344651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 9	NC_000009.11:g.132106908_132106929=	NC_000009.11:g.132106914_132106929del	NC_000009.11:g.132106917_132106929del	NC_000009.11:g.132106918_132106929del	NC_000009.11:g.132106919_132106929del	NC_000009.11:g.132106920_132106929del	NC_000009.11:g.132106922_132106929del	NC_000009.11:g.132106923_132106929del	NC_000009.11:g.132106924_132106929del	NC_000009.11:g.132106925_132106929del	NC_000009.11:g.132106926_132106929del	NC_000009.11:g.132106927_132106929del	NC_000009.11:g.132106928_132106929del	NC_000009.11:g.132106929del	NC_000009.11:g.132106929dup	NC_000009.11:g.132106928_132106929dup	NC_000009.11:g.132106927_132106929dup	NC_000009.11:g.132106926_132106929dup	NC_000009.11:g.132106925_132106929dup	NC_000009.11:g.132106924_132106929dup	NC_000009.11:g.132106923_132106929dup	NC_000009.11:g.132106922_132106929dup	NC_000009.11:g.132106921_132106929dup	NC_000009.11:g.132106920_132106929dup	NC_000009.11:g.132106919_132106929dup	NC_000009.11:g.132106918_132106929dup	NC_000009.11:g.132106917_132106929dup	NC_000009.11:g.132106916_132106929dup	NC_000009.11:g.132106915_132106929dup	NC_000009.11:g.132106914_132106929dup	NC_000009.11:g.132106913_132106929dup	NC_000009.11:g.132106912_132106929dup	NC_000009.11:g.132106911_132106929dup	NC_000009.11:g.132106910_132106929dup	NC_000009.11:g.132106909_132106929dup	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.11:g.132106929_132106930insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

81 SubSNP, 56 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss295441300	Oct 12, 2018 (152)
2	SSMP	ss663902359	Apr 01, 2015 (144)
3	SWEGEN	ss3005656640	Jan 10, 2018 (151)
4	SWEGEN	ss3005656641	Jan 10, 2018 (151)
5	SWEGEN	ss3005656642	Jan 10, 2018 (151)
6	SWEGEN	ss3005656643	Jan 10, 2018 (151)
7	EVA_DECODE	ss3724831194	Jul 13, 2019 (153)
8	EVA_DECODE	ss3724831195	Jul 13, 2019 (153)
9	EVA_DECODE	ss3724831196	Jul 13, 2019 (153)
10	EVA_DECODE	ss3724831197	Jul 13, 2019 (153)
11	EVA_DECODE	ss3724831198	Jul 13, 2019 (153)
12	PACBIO	ss3796612272	Jul 13, 2019 (153)
13	EVA	ss3831878497	Apr 26, 2020 (154)
14	KOGIC	ss3966838000	Apr 26, 2020 (154)
15	KOGIC	ss3966838001	Apr 26, 2020 (154)
16	KOGIC	ss3966838002	Apr 26, 2020 (154)
17	KOGIC	ss3966838003	Apr 26, 2020 (154)
18	KOGIC	ss3966838004	Apr 26, 2020 (154)
19	KOGIC	ss3966838005	Apr 26, 2020 (154)
20	GNOMAD	ss4210138266	Apr 26, 2021 (155)
21	GNOMAD	ss4210138267	Apr 26, 2021 (155)
22	GNOMAD	ss4210138268	Apr 26, 2021 (155)
23	GNOMAD	ss4210138269	Apr 26, 2021 (155)
24	GNOMAD	ss4210138270	Apr 26, 2021 (155)
25	GNOMAD	ss4210138271	Apr 26, 2021 (155)
26	GNOMAD	ss4210138272	Apr 26, 2021 (155)
27	GNOMAD	ss4210138273	Apr 26, 2021 (155)
28	GNOMAD	ss4210138274	Apr 26, 2021 (155)
29	GNOMAD	ss4210138275	Apr 26, 2021 (155)
30	GNOMAD	ss4210138276	Apr 26, 2021 (155)
31	GNOMAD	ss4210138277	Apr 26, 2021 (155)
32	GNOMAD	ss4210138278	Apr 26, 2021 (155)
33	GNOMAD	ss4210138279	Apr 26, 2021 (155)
34	GNOMAD	ss4210138280	Apr 26, 2021 (155)
35	GNOMAD	ss4210138281	Apr 26, 2021 (155)
36	GNOMAD	ss4210138282	Apr 26, 2021 (155)
37	GNOMAD	ss4210138283	Apr 26, 2021 (155)
38	GNOMAD	ss4210138284	Apr 26, 2021 (155)
39	GNOMAD	ss4210138285	Apr 26, 2021 (155)
40	GNOMAD	ss4210138286	Apr 26, 2021 (155)
41	GNOMAD	ss4210138287	Apr 26, 2021 (155)
42	GNOMAD	ss4210138288	Apr 26, 2021 (155)
43	GNOMAD	ss4210138289	Apr 26, 2021 (155)
44	GNOMAD	ss4210138290	Apr 26, 2021 (155)
45	GNOMAD	ss4210138291	Apr 26, 2021 (155)
46	GNOMAD	ss4210138292	Apr 26, 2021 (155)
47	GNOMAD	ss4210138293	Apr 26, 2021 (155)
48	GNOMAD	ss4210138294	Apr 26, 2021 (155)
49	GNOMAD	ss4210138295	Apr 26, 2021 (155)
50	GNOMAD	ss4210138296	Apr 26, 2021 (155)
51	GNOMAD	ss4210138297	Apr 26, 2021 (155)
52	GNOMAD	ss4210138298	Apr 26, 2021 (155)
53	GNOMAD	ss4210138299	Apr 26, 2021 (155)
54	GNOMAD	ss4210138300	Apr 26, 2021 (155)
55	GNOMAD	ss4210138301	Apr 26, 2021 (155)
56	TOPMED	ss4837093947	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5195488532	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5195488533	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5195488534	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5195488535	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5195488536	Apr 26, 2021 (155)
62	TOMMO_GENOMICS	ss5195488537	Apr 26, 2021 (155)
63	1000G_HIGH_COVERAGE	ss5282318984	Oct 13, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5282318985	Oct 13, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5282318986	Oct 13, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5282318987	Oct 13, 2022 (156)
67	1000G_HIGH_COVERAGE	ss5282318988	Oct 13, 2022 (156)
68	1000G_HIGH_COVERAGE	ss5282318989	Oct 13, 2022 (156)
69	HUGCELL_USP	ss5478173407	Oct 13, 2022 (156)
70	HUGCELL_USP	ss5478173408	Oct 13, 2022 (156)
71	HUGCELL_USP	ss5478173409	Oct 13, 2022 (156)
72	HUGCELL_USP	ss5478173410	Oct 13, 2022 (156)
73	HUGCELL_USP	ss5478173411	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5740079180	Oct 13, 2022 (156)
75	TOMMO_GENOMICS	ss5740079181	Oct 13, 2022 (156)
76	TOMMO_GENOMICS	ss5740079182	Oct 13, 2022 (156)
77	TOMMO_GENOMICS	ss5740079183	Oct 13, 2022 (156)
78	TOMMO_GENOMICS	ss5740079184	Oct 13, 2022 (156)
79	TOMMO_GENOMICS	ss5740079185	Oct 13, 2022 (156)
80	EVA	ss5829803034	Oct 13, 2022 (156)
81	EVA	ss5829803035	Oct 13, 2022 (156)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
111	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
112	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
113	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
114	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
115	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
116	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
117	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338840723 (NC_000009.12:129344628::A 3705/50490) Row 338840724 (NC_000009.12:129344628::AA 9948/50492) Row 338840725 (NC_000009.12:129344628::AAA 2908/50690)...	-	Apr 26, 2021 (155)
118	Korean Genome Project Submission ignored due to conflicting rows: Row 23216001 (NC_000009.12:129344630::AA 205/1616) Row 23216002 (NC_000009.12:129344630::AAA 68/1616) Row 23216003 (NC_000009.12:129344630::AAAAA 37/1616)...	-	Apr 26, 2020 (154)
119	Korean Genome Project Submission ignored due to conflicting rows: Row 23216001 (NC_000009.12:129344630::AA 205/1616) Row 23216002 (NC_000009.12:129344630::AAA 68/1616) Row 23216003 (NC_000009.12:129344630::AAAAA 37/1616)...	-	Apr 26, 2020 (154)
120	Korean Genome Project Submission ignored due to conflicting rows: Row 23216001 (NC_000009.12:129344630::AA 205/1616) Row 23216002 (NC_000009.12:129344630::AAA 68/1616) Row 23216003 (NC_000009.12:129344630::AAAAA 37/1616)...	-	Apr 26, 2020 (154)
121	Korean Genome Project Submission ignored due to conflicting rows: Row 23216001 (NC_000009.12:129344630::AA 205/1616) Row 23216002 (NC_000009.12:129344630::AAA 68/1616) Row 23216003 (NC_000009.12:129344630::AAAAA 37/1616)...	-	Apr 26, 2020 (154)
122	Korean Genome Project Submission ignored due to conflicting rows: Row 23216001 (NC_000009.12:129344630::AA 205/1616) Row 23216002 (NC_000009.12:129344630::AAA 68/1616) Row 23216003 (NC_000009.12:129344630::AAAAA 37/1616)...	-	Apr 26, 2020 (154)
123	Korean Genome Project Submission ignored due to conflicting rows: Row 23216001 (NC_000009.12:129344630::AA 205/1616) Row 23216002 (NC_000009.12:129344630::AAA 68/1616) Row 23216003 (NC_000009.12:129344630::AAAAA 37/1616)...	-	Apr 26, 2020 (154)
124	8.3KJPN Submission ignored due to conflicting rows: Row 53457839 (NC_000009.11:132106907::AA 1354/15080) Row 53457840 (NC_000009.11:132106907::AAAA 1750/15080) Row 53457841 (NC_000009.11:132106907:AA: 524/15080)...	-	Apr 26, 2021 (155)
125	8.3KJPN Submission ignored due to conflicting rows: Row 53457839 (NC_000009.11:132106907::AA 1354/15080) Row 53457840 (NC_000009.11:132106907::AAAA 1750/15080) Row 53457841 (NC_000009.11:132106907:AA: 524/15080)...	-	Apr 26, 2021 (155)
126	8.3KJPN Submission ignored due to conflicting rows: Row 53457839 (NC_000009.11:132106907::AA 1354/15080) Row 53457840 (NC_000009.11:132106907::AAAA 1750/15080) Row 53457841 (NC_000009.11:132106907:AA: 524/15080)...	-	Apr 26, 2021 (155)
127	8.3KJPN Submission ignored due to conflicting rows: Row 53457839 (NC_000009.11:132106907::AA 1354/15080) Row 53457840 (NC_000009.11:132106907::AAAA 1750/15080) Row 53457841 (NC_000009.11:132106907:AA: 524/15080)...	-	Apr 26, 2021 (155)
128	8.3KJPN Submission ignored due to conflicting rows: Row 53457839 (NC_000009.11:132106907::AA 1354/15080) Row 53457840 (NC_000009.11:132106907::AAAA 1750/15080) Row 53457841 (NC_000009.11:132106907:AA: 524/15080)...	-	Apr 26, 2021 (155)
129	8.3KJPN Submission ignored due to conflicting rows: Row 53457839 (NC_000009.11:132106907::AA 1354/15080) Row 53457840 (NC_000009.11:132106907::AAAA 1750/15080) Row 53457841 (NC_000009.11:132106907:AA: 524/15080)...	-	Apr 26, 2021 (155)
130	14KJPN Submission ignored due to conflicting rows: Row 73916284 (NC_000009.12:129344628::AA 1902/22452) Row 73916285 (NC_000009.12:129344628:A: 161/22452) Row 73916286 (NC_000009.12:129344628:AA: 819/22452)...	-	Oct 13, 2022 (156)
131	14KJPN Submission ignored due to conflicting rows: Row 73916284 (NC_000009.12:129344628::AA 1902/22452) Row 73916285 (NC_000009.12:129344628:A: 161/22452) Row 73916286 (NC_000009.12:129344628:AA: 819/22452)...	-	Oct 13, 2022 (156)
132	14KJPN Submission ignored due to conflicting rows: Row 73916284 (NC_000009.12:129344628::AA 1902/22452) Row 73916285 (NC_000009.12:129344628:A: 161/22452) Row 73916286 (NC_000009.12:129344628:AA: 819/22452)...	-	Oct 13, 2022 (156)
133	14KJPN Submission ignored due to conflicting rows: Row 73916284 (NC_000009.12:129344628::AA 1902/22452) Row 73916285 (NC_000009.12:129344628:A: 161/22452) Row 73916286 (NC_000009.12:129344628:AA: 819/22452)...	-	Oct 13, 2022 (156)
134	14KJPN Submission ignored due to conflicting rows: Row 73916284 (NC_000009.12:129344628::AA 1902/22452) Row 73916285 (NC_000009.12:129344628:A: 161/22452) Row 73916286 (NC_000009.12:129344628:AA: 819/22452)...	-	Oct 13, 2022 (156)
135	14KJPN Submission ignored due to conflicting rows: Row 73916284 (NC_000009.12:129344628::AA 1902/22452) Row 73916285 (NC_000009.12:129344628:A: 161/22452) Row 73916286 (NC_000009.12:129344628:AA: 819/22452)...	-	Oct 13, 2022 (156)
136	TopMed	NC_000009.12 - 129344629	Apr 26, 2021 (155)
137	ALFA	NC_000009.12 - 129344629	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
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAA	(self)
ss4210138301	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4210138300	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
674471508, ss4210138299, ss4837093947	NC_000009.12:129344628:AAAAAAAAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4210138298	NC_000009.12:129344628:AAAAAAAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4210138297	NC_000009.12:129344628:AAAAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4210138296	NC_000009.12:129344628:AAAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5195488536	NC_000009.11:132106907:AAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4210138295, ss5740079184	NC_000009.12:129344628:AAAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4210138294	NC_000009.12:129344628:AAAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4210138293	NC_000009.12:129344628:AAA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5195488534	NC_000009.11:132106907:AA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3966838003, ss4210138292, ss5282318989, ss5740079182	NC_000009.12:129344628:AA:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5195488535	NC_000009.11:132106907:A:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3724831198, ss4210138291, ss5282318986, ss5478173411, ss5740079181	NC_000009.12:129344628:A:	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss295441300	NC_000009.10:131146750::A	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3005656643, ss3796612272, ss5195488537	NC_000009.11:132106907::A	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138266, ss5282318985, ss5478173407, ss5740079185	NC_000009.12:129344628::A	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3724831197	NC_000009.12:129344629::A	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3966838004	NC_000009.12:129344630::A	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss663902359, ss3005656640, ss3831878497, ss5195488532, ss5829803034	NC_000009.11:132106907::AA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138267, ss5282318984, ss5478173408, ss5740079180	NC_000009.12:129344628::AA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3724831196	NC_000009.12:129344629::AA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3966838000	NC_000009.12:129344630::AA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3005656642, ss5829803035	NC_000009.11:132106907::AAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138268, ss5282318987, ss5478173409	NC_000009.12:129344628::AAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3724831195	NC_000009.12:129344629::AAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3966838001	NC_000009.12:129344630::AAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3005656641, ss5195488533	NC_000009.11:132106907::AAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138269, ss5282318988, ss5478173410, ss5740079183	NC_000009.12:129344628::AAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3724831194	NC_000009.12:129344629::AAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3966838005	NC_000009.12:129344630::AAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138270	NC_000009.12:129344628::AAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3966838002	NC_000009.12:129344630::AAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138271	NC_000009.12:129344628::AAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138272	NC_000009.12:129344628::AAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13510025986	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138273	NC_000009.12:129344628::AAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138274	NC_000009.12:129344628::AAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138275	NC_000009.12:129344628::AAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138276	NC_000009.12:129344628::AAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138277	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138278	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138279	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138280	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138281	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138282	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138283	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138284	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138285	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138286	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138287	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138288	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138289	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4210138290	NC_000009.12:129344628::AAAAAAAAAA… NC_000009.12:129344628::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:129344628:AAAAAAAAAAA… NC_000009.12:129344628:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs773774279

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

rs773774279