Name: rs56101324
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.

rs56101324

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:35738287-35738296 (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: delGG / delG / dupG / dupGG / dupG…
delGG / delG / dupG / dupGG / dupGGG / dup(G)₄ / dup(G)₅ / dup(G)₆ / dup(G)₇ / dup(G)₈ / dup(G)₉ / dup(G)₁₀ / ins(G)₁₁ / ins(G)₁₂ / ins(G)₁₃ / ins(G)₁₄ / ins(G)₁₅ / ins(G)₁₆ / ins(G)₁₇
Variation Type: Indel Insertion and Deletion
Frequency: delG=0.2049 (1026/5008, 1000G)
delGG=0.0000 (0/4816, ALFA)
delG=0.0000 (0/4816, ALFA) (+ 5 more)
dupG=0.0000 (0/4816, ALFA)
dupGG=0.0000 (0/4816, ALFA)
dupGGG=0.0000 (0/4816, ALFA)
dup(G)₄=0.0000 (0/4816, ALFA)
dup(G)₅=0.0000 (0/4816, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ARMC12 : Intron Variant
LOC285847 : 2KB Upstream 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	4816	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
European	Sub	3110	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
African	Sub	1182	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
African Others	Sub	60	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
African American	Sub	1122	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
Asian	Sub	58	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
East Asian	Sub	42	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Other Asian	Sub	16	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 1	Sub	68	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 2	Sub	170	GGGGGGGGGG=1.000	GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000	1.0	N/A
South Asian	Sub	48	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Other	Sub	180	GGGGGGGGGG=1.000	GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=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
1000Genomes	Global	Study-wide	5008	(G)₁₀=0.7951	delG=0.2049
1000Genomes	African	Sub	1322	(G)₁₀=0.7065	delG=0.2935
1000Genomes	East Asian	Sub	1008	(G)₁₀=0.7331	delG=0.2669
1000Genomes	Europe	Sub	1006	(G)₁₀=0.8807	delG=0.1193
1000Genomes	South Asian	Sub	978	(G)₁₀=0.844	delG=0.156
1000Genomes	American	Sub	694	(G)₁₀=0.862	delG=0.138
Allele Frequency Aggregator	Total	Global	4816	(G)₁₀=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	European	Sub	3110	(G)₁₀=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	African	Sub	1182	(G)₁₀=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	Other	Sub	180	(G)₁₀=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	170	(G)₁₀=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	68	(G)₁₀=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00
Allele Frequency Aggregator	Asian	Sub	58	(G)₁₀=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	48	(G)₁₀=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=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 6	NC_000006.12:g.35738295_35738296del
GRCh38.p14 chr 6	NC_000006.12:g.35738296del
GRCh38.p14 chr 6	NC_000006.12:g.35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738295_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738294_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738293_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738292_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738291_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738290_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738289_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738288_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738287_35738296dup
GRCh38.p14 chr 6	NC_000006.12:g.35738296_35738297insGGGGGGGGGGG
GRCh38.p14 chr 6	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGG
GRCh38.p14 chr 6	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGG
GRCh38.p14 chr 6	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGG
GRCh38.p14 chr 6	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGG
GRCh38.p14 chr 6	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGGG
GRCh38.p14 chr 6	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706072_35706073del
GRCh37.p13 chr 6	NC_000006.11:g.35706073del
GRCh37.p13 chr 6	NC_000006.11:g.35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706072_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706071_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706070_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706069_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706068_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706067_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706066_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706065_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706064_35706073dup
GRCh37.p13 chr 6	NC_000006.11:g.35706073_35706074insGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9570_9571del
ARMC12 RefSeqGene	NG_052798.1:g.9571del
ARMC12 RefSeqGene	NG_052798.1:g.9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9570_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9569_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9568_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9567_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9566_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9565_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9564_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9563_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9562_9571dup
ARMC12 RefSeqGene	NG_052798.1:g.9571_9572insGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9571_9572insGGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9571_9572insGGGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGGGG

Gene: ARMC12, armadillo repeat containing 12 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ARMC12 transcript variant 2	NM_001286574.2:c.310-89_3… NM_001286574.2:c.310-89_310-88del	N/A	Intron Variant
ARMC12 transcript variant 3	NM_001286576.2:c.310-89_3… NM_001286576.2:c.310-89_310-88del	N/A	Intron Variant
ARMC12 transcript variant 1	NM_145028.5:c.391-89_391-… NM_145028.5:c.391-89_391-88del	N/A	Intron Variant
ARMC12 transcript variant X2	XM_011514381.3:c.196-89_1… XM_011514381.3:c.196-89_196-88del	N/A	Intron Variant
ARMC12 transcript variant X3	XM_011514382.3:c.49-89_49… XM_011514382.3:c.49-89_49-88del	N/A	Intron Variant
ARMC12 transcript variant X4	XM_017010435.3:c.391-89_3… XM_017010435.3:c.391-89_391-88del	N/A	Intron Variant
ARMC12 transcript variant X5	XM_047418343.1:c.391-89_3… XM_047418343.1:c.391-89_391-88del	N/A	Intron Variant
ARMC12 transcript variant X6	XM_047418344.1:c.391-89_3… XM_047418344.1:c.391-89_391-88del	N/A	Intron Variant
ARMC12 transcript variant X7	XM_047418345.1:c.391-89_3… XM_047418345.1:c.391-89_391-88del	N/A	Intron Variant
ARMC12 transcript variant X8	XM_047418346.1:c.391-89_3… XM_047418346.1:c.391-89_391-88del	N/A	Intron Variant
ARMC12 transcript variant X9	XM_047418347.1:c.310-89_3… XM_047418347.1:c.310-89_310-88del	N/A	Intron Variant
ARMC12 transcript variant X1	XM_047418348.1:c.310-89_3… XM_047418348.1:c.310-89_310-88del	N/A	Intron Variant

Gene: LOC285847, uncharacterized LOC285847 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC285847 transcript	NR_027117.2:n.	N/A	Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(G)₁₀=	delGG	delG	dupG	dupGG	dupGGG	dup(G)₄	dup(G)₅	dup(G)₆	dup(G)₇	dup(G)₈	dup(G)₉	dup(G)₁₀	ins(G)₁₁	ins(G)₁₂	ins(G)₁₃	ins(G)₁₄	ins(G)₁₅	ins(G)₁₆	ins(G)₁₇
GRCh38.p14 chr 6	NC_000006.12:g.35738287_35738296=	NC_000006.12:g.35738295_35738296del	NC_000006.12:g.35738296del	NC_000006.12:g.35738296dup	NC_000006.12:g.35738295_35738296dup	NC_000006.12:g.35738294_35738296dup	NC_000006.12:g.35738293_35738296dup	NC_000006.12:g.35738292_35738296dup	NC_000006.12:g.35738291_35738296dup	NC_000006.12:g.35738290_35738296dup	NC_000006.12:g.35738289_35738296dup	NC_000006.12:g.35738288_35738296dup	NC_000006.12:g.35738287_35738296dup	NC_000006.12:g.35738296_35738297insGGGGGGGGGGG	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGG	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGG	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGG	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGG	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGGG	NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 6	NC_000006.11:g.35706064_35706073=	NC_000006.11:g.35706072_35706073del	NC_000006.11:g.35706073del	NC_000006.11:g.35706073dup	NC_000006.11:g.35706072_35706073dup	NC_000006.11:g.35706071_35706073dup	NC_000006.11:g.35706070_35706073dup	NC_000006.11:g.35706069_35706073dup	NC_000006.11:g.35706068_35706073dup	NC_000006.11:g.35706067_35706073dup	NC_000006.11:g.35706066_35706073dup	NC_000006.11:g.35706065_35706073dup	NC_000006.11:g.35706064_35706073dup	NC_000006.11:g.35706073_35706074insGGGGGGGGGGG	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGG	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGG	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGG	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGG	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGGG	NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGGGG
ARMC12 RefSeqGene	NG_052798.1:g.9562_9571=	NG_052798.1:g.9570_9571del	NG_052798.1:g.9571del	NG_052798.1:g.9571dup	NG_052798.1:g.9570_9571dup	NG_052798.1:g.9569_9571dup	NG_052798.1:g.9568_9571dup	NG_052798.1:g.9567_9571dup	NG_052798.1:g.9566_9571dup	NG_052798.1:g.9565_9571dup	NG_052798.1:g.9564_9571dup	NG_052798.1:g.9563_9571dup	NG_052798.1:g.9562_9571dup	NG_052798.1:g.9571_9572insGGGGGGGGGGG	NG_052798.1:g.9571_9572insGGGGGGGGGGGG	NG_052798.1:g.9571_9572insGGGGGGGGGGGGG	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGG	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGG	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGGG	NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant 2	NM_001286574.2:c.310-97=	NM_001286574.2:c.310-89_310-88del	NM_001286574.2:c.310-88del	NM_001286574.2:c.310-88dup	NM_001286574.2:c.310-89_310-88dup	NM_001286574.2:c.310-90_310-88dup	NM_001286574.2:c.310-91_310-88dup	NM_001286574.2:c.310-92_310-88dup	NM_001286574.2:c.310-93_310-88dup	NM_001286574.2:c.310-94_310-88dup	NM_001286574.2:c.310-95_310-88dup	NM_001286574.2:c.310-96_310-88dup	NM_001286574.2:c.310-97_310-88dup	NM_001286574.2:c.310-88_310-87insGGGGGGGGGGG	NM_001286574.2:c.310-88_310-87insGGGGGGGGGGGG	NM_001286574.2:c.310-88_310-87insGGGGGGGGGGGGG	NM_001286574.2:c.310-88_310-87insGGGGGGGGGGGGGG	NM_001286574.2:c.310-88_310-87insGGGGGGGGGGGGGGG	NM_001286574.2:c.310-88_310-87insGGGGGGGGGGGGGGGG	NM_001286574.2:c.310-88_310-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant 3	NM_001286576.2:c.310-97=	NM_001286576.2:c.310-89_310-88del	NM_001286576.2:c.310-88del	NM_001286576.2:c.310-88dup	NM_001286576.2:c.310-89_310-88dup	NM_001286576.2:c.310-90_310-88dup	NM_001286576.2:c.310-91_310-88dup	NM_001286576.2:c.310-92_310-88dup	NM_001286576.2:c.310-93_310-88dup	NM_001286576.2:c.310-94_310-88dup	NM_001286576.2:c.310-95_310-88dup	NM_001286576.2:c.310-96_310-88dup	NM_001286576.2:c.310-97_310-88dup	NM_001286576.2:c.310-88_310-87insGGGGGGGGGGG	NM_001286576.2:c.310-88_310-87insGGGGGGGGGGGG	NM_001286576.2:c.310-88_310-87insGGGGGGGGGGGGG	NM_001286576.2:c.310-88_310-87insGGGGGGGGGGGGGG	NM_001286576.2:c.310-88_310-87insGGGGGGGGGGGGGGG	NM_001286576.2:c.310-88_310-87insGGGGGGGGGGGGGGGG	NM_001286576.2:c.310-88_310-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript	NM_145028.3:c.391-97=	NM_145028.3:c.391-89_391-88del	NM_145028.3:c.391-88del	NM_145028.3:c.391-88dup	NM_145028.3:c.391-89_391-88dup	NM_145028.3:c.391-90_391-88dup	NM_145028.3:c.391-91_391-88dup	NM_145028.3:c.391-92_391-88dup	NM_145028.3:c.391-93_391-88dup	NM_145028.3:c.391-94_391-88dup	NM_145028.3:c.391-95_391-88dup	NM_145028.3:c.391-96_391-88dup	NM_145028.3:c.391-97_391-88dup	NM_145028.3:c.391-88_391-87insGGGGGGGGGGG	NM_145028.3:c.391-88_391-87insGGGGGGGGGGGG	NM_145028.3:c.391-88_391-87insGGGGGGGGGGGGG	NM_145028.3:c.391-88_391-87insGGGGGGGGGGGGGG	NM_145028.3:c.391-88_391-87insGGGGGGGGGGGGGGG	NM_145028.3:c.391-88_391-87insGGGGGGGGGGGGGGGG	NM_145028.3:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant 1	NM_145028.5:c.391-97=	NM_145028.5:c.391-89_391-88del	NM_145028.5:c.391-88del	NM_145028.5:c.391-88dup	NM_145028.5:c.391-89_391-88dup	NM_145028.5:c.391-90_391-88dup	NM_145028.5:c.391-91_391-88dup	NM_145028.5:c.391-92_391-88dup	NM_145028.5:c.391-93_391-88dup	NM_145028.5:c.391-94_391-88dup	NM_145028.5:c.391-95_391-88dup	NM_145028.5:c.391-96_391-88dup	NM_145028.5:c.391-97_391-88dup	NM_145028.5:c.391-88_391-87insGGGGGGGGGGG	NM_145028.5:c.391-88_391-87insGGGGGGGGGGGG	NM_145028.5:c.391-88_391-87insGGGGGGGGGGGGG	NM_145028.5:c.391-88_391-87insGGGGGGGGGGGGGG	NM_145028.5:c.391-88_391-87insGGGGGGGGGGGGGGG	NM_145028.5:c.391-88_391-87insGGGGGGGGGGGGGGGG	NM_145028.5:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X1	XM_005248919.1:c.391-97=	XM_005248919.1:c.391-89_391-88del	XM_005248919.1:c.391-88del	XM_005248919.1:c.391-88dup	XM_005248919.1:c.391-89_391-88dup	XM_005248919.1:c.391-90_391-88dup	XM_005248919.1:c.391-91_391-88dup	XM_005248919.1:c.391-92_391-88dup	XM_005248919.1:c.391-93_391-88dup	XM_005248919.1:c.391-94_391-88dup	XM_005248919.1:c.391-95_391-88dup	XM_005248919.1:c.391-96_391-88dup	XM_005248919.1:c.391-97_391-88dup	XM_005248919.1:c.391-88_391-87insGGGGGGGGGGG	XM_005248919.1:c.391-88_391-87insGGGGGGGGGGGG	XM_005248919.1:c.391-88_391-87insGGGGGGGGGGGGG	XM_005248919.1:c.391-88_391-87insGGGGGGGGGGGGGG	XM_005248919.1:c.391-88_391-87insGGGGGGGGGGGGGGG	XM_005248919.1:c.391-88_391-87insGGGGGGGGGGGGGGGG	XM_005248919.1:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X2	XM_005248920.1:c.391-97=	XM_005248920.1:c.391-89_391-88del	XM_005248920.1:c.391-88del	XM_005248920.1:c.391-88dup	XM_005248920.1:c.391-89_391-88dup	XM_005248920.1:c.391-90_391-88dup	XM_005248920.1:c.391-91_391-88dup	XM_005248920.1:c.391-92_391-88dup	XM_005248920.1:c.391-93_391-88dup	XM_005248920.1:c.391-94_391-88dup	XM_005248920.1:c.391-95_391-88dup	XM_005248920.1:c.391-96_391-88dup	XM_005248920.1:c.391-97_391-88dup	XM_005248920.1:c.391-88_391-87insGGGGGGGGGGG	XM_005248920.1:c.391-88_391-87insGGGGGGGGGGGG	XM_005248920.1:c.391-88_391-87insGGGGGGGGGGGGG	XM_005248920.1:c.391-88_391-87insGGGGGGGGGGGGGG	XM_005248920.1:c.391-88_391-87insGGGGGGGGGGGGGGG	XM_005248920.1:c.391-88_391-87insGGGGGGGGGGGGGGGG	XM_005248920.1:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X3	XM_005248921.1:c.310-97=	XM_005248921.1:c.310-89_310-88del	XM_005248921.1:c.310-88del	XM_005248921.1:c.310-88dup	XM_005248921.1:c.310-89_310-88dup	XM_005248921.1:c.310-90_310-88dup	XM_005248921.1:c.310-91_310-88dup	XM_005248921.1:c.310-92_310-88dup	XM_005248921.1:c.310-93_310-88dup	XM_005248921.1:c.310-94_310-88dup	XM_005248921.1:c.310-95_310-88dup	XM_005248921.1:c.310-96_310-88dup	XM_005248921.1:c.310-97_310-88dup	XM_005248921.1:c.310-88_310-87insGGGGGGGGGGG	XM_005248921.1:c.310-88_310-87insGGGGGGGGGGGG	XM_005248921.1:c.310-88_310-87insGGGGGGGGGGGGG	XM_005248921.1:c.310-88_310-87insGGGGGGGGGGGGGG	XM_005248921.1:c.310-88_310-87insGGGGGGGGGGGGGGG	XM_005248921.1:c.310-88_310-87insGGGGGGGGGGGGGGGG	XM_005248921.1:c.310-88_310-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X4	XM_005248922.1:c.310-97=	XM_005248922.1:c.310-89_310-88del	XM_005248922.1:c.310-88del	XM_005248922.1:c.310-88dup	XM_005248922.1:c.310-89_310-88dup	XM_005248922.1:c.310-90_310-88dup	XM_005248922.1:c.310-91_310-88dup	XM_005248922.1:c.310-92_310-88dup	XM_005248922.1:c.310-93_310-88dup	XM_005248922.1:c.310-94_310-88dup	XM_005248922.1:c.310-95_310-88dup	XM_005248922.1:c.310-96_310-88dup	XM_005248922.1:c.310-97_310-88dup	XM_005248922.1:c.310-88_310-87insGGGGGGGGGGG	XM_005248922.1:c.310-88_310-87insGGGGGGGGGGGG	XM_005248922.1:c.310-88_310-87insGGGGGGGGGGGGG	XM_005248922.1:c.310-88_310-87insGGGGGGGGGGGGGG	XM_005248922.1:c.310-88_310-87insGGGGGGGGGGGGGGG	XM_005248922.1:c.310-88_310-87insGGGGGGGGGGGGGGGG	XM_005248922.1:c.310-88_310-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X2	XM_011514381.3:c.196-97=	XM_011514381.3:c.196-89_196-88del	XM_011514381.3:c.196-88del	XM_011514381.3:c.196-88dup	XM_011514381.3:c.196-89_196-88dup	XM_011514381.3:c.196-90_196-88dup	XM_011514381.3:c.196-91_196-88dup	XM_011514381.3:c.196-92_196-88dup	XM_011514381.3:c.196-93_196-88dup	XM_011514381.3:c.196-94_196-88dup	XM_011514381.3:c.196-95_196-88dup	XM_011514381.3:c.196-96_196-88dup	XM_011514381.3:c.196-97_196-88dup	XM_011514381.3:c.196-88_196-87insGGGGGGGGGGG	XM_011514381.3:c.196-88_196-87insGGGGGGGGGGGG	XM_011514381.3:c.196-88_196-87insGGGGGGGGGGGGG	XM_011514381.3:c.196-88_196-87insGGGGGGGGGGGGGG	XM_011514381.3:c.196-88_196-87insGGGGGGGGGGGGGGG	XM_011514381.3:c.196-88_196-87insGGGGGGGGGGGGGGGG	XM_011514381.3:c.196-88_196-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X3	XM_011514382.3:c.49-97=	XM_011514382.3:c.49-89_49-88del	XM_011514382.3:c.49-88del	XM_011514382.3:c.49-88dup	XM_011514382.3:c.49-89_49-88dup	XM_011514382.3:c.49-90_49-88dup	XM_011514382.3:c.49-91_49-88dup	XM_011514382.3:c.49-92_49-88dup	XM_011514382.3:c.49-93_49-88dup	XM_011514382.3:c.49-94_49-88dup	XM_011514382.3:c.49-95_49-88dup	XM_011514382.3:c.49-96_49-88dup	XM_011514382.3:c.49-97_49-88dup	XM_011514382.3:c.49-88_49-87insGGGGGGGGGGG	XM_011514382.3:c.49-88_49-87insGGGGGGGGGGGG	XM_011514382.3:c.49-88_49-87insGGGGGGGGGGGGG	XM_011514382.3:c.49-88_49-87insGGGGGGGGGGGGGG	XM_011514382.3:c.49-88_49-87insGGGGGGGGGGGGGGG	XM_011514382.3:c.49-88_49-87insGGGGGGGGGGGGGGGG	XM_011514382.3:c.49-88_49-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X4	XM_017010435.3:c.391-97=	XM_017010435.3:c.391-89_391-88del	XM_017010435.3:c.391-88del	XM_017010435.3:c.391-88dup	XM_017010435.3:c.391-89_391-88dup	XM_017010435.3:c.391-90_391-88dup	XM_017010435.3:c.391-91_391-88dup	XM_017010435.3:c.391-92_391-88dup	XM_017010435.3:c.391-93_391-88dup	XM_017010435.3:c.391-94_391-88dup	XM_017010435.3:c.391-95_391-88dup	XM_017010435.3:c.391-96_391-88dup	XM_017010435.3:c.391-97_391-88dup	XM_017010435.3:c.391-88_391-87insGGGGGGGGGGG	XM_017010435.3:c.391-88_391-87insGGGGGGGGGGGG	XM_017010435.3:c.391-88_391-87insGGGGGGGGGGGGG	XM_017010435.3:c.391-88_391-87insGGGGGGGGGGGGGG	XM_017010435.3:c.391-88_391-87insGGGGGGGGGGGGGGG	XM_017010435.3:c.391-88_391-87insGGGGGGGGGGGGGGGG	XM_017010435.3:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X5	XM_047418343.1:c.391-97=	XM_047418343.1:c.391-89_391-88del	XM_047418343.1:c.391-88del	XM_047418343.1:c.391-88dup	XM_047418343.1:c.391-89_391-88dup	XM_047418343.1:c.391-90_391-88dup	XM_047418343.1:c.391-91_391-88dup	XM_047418343.1:c.391-92_391-88dup	XM_047418343.1:c.391-93_391-88dup	XM_047418343.1:c.391-94_391-88dup	XM_047418343.1:c.391-95_391-88dup	XM_047418343.1:c.391-96_391-88dup	XM_047418343.1:c.391-97_391-88dup	XM_047418343.1:c.391-88_391-87insGGGGGGGGGGG	XM_047418343.1:c.391-88_391-87insGGGGGGGGGGGG	XM_047418343.1:c.391-88_391-87insGGGGGGGGGGGGG	XM_047418343.1:c.391-88_391-87insGGGGGGGGGGGGGG	XM_047418343.1:c.391-88_391-87insGGGGGGGGGGGGGGG	XM_047418343.1:c.391-88_391-87insGGGGGGGGGGGGGGGG	XM_047418343.1:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X6	XM_047418344.1:c.391-97=	XM_047418344.1:c.391-89_391-88del	XM_047418344.1:c.391-88del	XM_047418344.1:c.391-88dup	XM_047418344.1:c.391-89_391-88dup	XM_047418344.1:c.391-90_391-88dup	XM_047418344.1:c.391-91_391-88dup	XM_047418344.1:c.391-92_391-88dup	XM_047418344.1:c.391-93_391-88dup	XM_047418344.1:c.391-94_391-88dup	XM_047418344.1:c.391-95_391-88dup	XM_047418344.1:c.391-96_391-88dup	XM_047418344.1:c.391-97_391-88dup	XM_047418344.1:c.391-88_391-87insGGGGGGGGGGG	XM_047418344.1:c.391-88_391-87insGGGGGGGGGGGG	XM_047418344.1:c.391-88_391-87insGGGGGGGGGGGGG	XM_047418344.1:c.391-88_391-87insGGGGGGGGGGGGGG	XM_047418344.1:c.391-88_391-87insGGGGGGGGGGGGGGG	XM_047418344.1:c.391-88_391-87insGGGGGGGGGGGGGGGG	XM_047418344.1:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X7	XM_047418345.1:c.391-97=	XM_047418345.1:c.391-89_391-88del	XM_047418345.1:c.391-88del	XM_047418345.1:c.391-88dup	XM_047418345.1:c.391-89_391-88dup	XM_047418345.1:c.391-90_391-88dup	XM_047418345.1:c.391-91_391-88dup	XM_047418345.1:c.391-92_391-88dup	XM_047418345.1:c.391-93_391-88dup	XM_047418345.1:c.391-94_391-88dup	XM_047418345.1:c.391-95_391-88dup	XM_047418345.1:c.391-96_391-88dup	XM_047418345.1:c.391-97_391-88dup	XM_047418345.1:c.391-88_391-87insGGGGGGGGGGG	XM_047418345.1:c.391-88_391-87insGGGGGGGGGGGG	XM_047418345.1:c.391-88_391-87insGGGGGGGGGGGGG	XM_047418345.1:c.391-88_391-87insGGGGGGGGGGGGGG	XM_047418345.1:c.391-88_391-87insGGGGGGGGGGGGGGG	XM_047418345.1:c.391-88_391-87insGGGGGGGGGGGGGGGG	XM_047418345.1:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X8	XM_047418346.1:c.391-97=	XM_047418346.1:c.391-89_391-88del	XM_047418346.1:c.391-88del	XM_047418346.1:c.391-88dup	XM_047418346.1:c.391-89_391-88dup	XM_047418346.1:c.391-90_391-88dup	XM_047418346.1:c.391-91_391-88dup	XM_047418346.1:c.391-92_391-88dup	XM_047418346.1:c.391-93_391-88dup	XM_047418346.1:c.391-94_391-88dup	XM_047418346.1:c.391-95_391-88dup	XM_047418346.1:c.391-96_391-88dup	XM_047418346.1:c.391-97_391-88dup	XM_047418346.1:c.391-88_391-87insGGGGGGGGGGG	XM_047418346.1:c.391-88_391-87insGGGGGGGGGGGG	XM_047418346.1:c.391-88_391-87insGGGGGGGGGGGGG	XM_047418346.1:c.391-88_391-87insGGGGGGGGGGGGGG	XM_047418346.1:c.391-88_391-87insGGGGGGGGGGGGGGG	XM_047418346.1:c.391-88_391-87insGGGGGGGGGGGGGGGG	XM_047418346.1:c.391-88_391-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X9	XM_047418347.1:c.310-97=	XM_047418347.1:c.310-89_310-88del	XM_047418347.1:c.310-88del	XM_047418347.1:c.310-88dup	XM_047418347.1:c.310-89_310-88dup	XM_047418347.1:c.310-90_310-88dup	XM_047418347.1:c.310-91_310-88dup	XM_047418347.1:c.310-92_310-88dup	XM_047418347.1:c.310-93_310-88dup	XM_047418347.1:c.310-94_310-88dup	XM_047418347.1:c.310-95_310-88dup	XM_047418347.1:c.310-96_310-88dup	XM_047418347.1:c.310-97_310-88dup	XM_047418347.1:c.310-88_310-87insGGGGGGGGGGG	XM_047418347.1:c.310-88_310-87insGGGGGGGGGGGG	XM_047418347.1:c.310-88_310-87insGGGGGGGGGGGGG	XM_047418347.1:c.310-88_310-87insGGGGGGGGGGGGGG	XM_047418347.1:c.310-88_310-87insGGGGGGGGGGGGGGG	XM_047418347.1:c.310-88_310-87insGGGGGGGGGGGGGGGG	XM_047418347.1:c.310-88_310-87insGGGGGGGGGGGGGGGGG
ARMC12 transcript variant X1	XM_047418348.1:c.310-97=	XM_047418348.1:c.310-89_310-88del	XM_047418348.1:c.310-88del	XM_047418348.1:c.310-88dup	XM_047418348.1:c.310-89_310-88dup	XM_047418348.1:c.310-90_310-88dup	XM_047418348.1:c.310-91_310-88dup	XM_047418348.1:c.310-92_310-88dup	XM_047418348.1:c.310-93_310-88dup	XM_047418348.1:c.310-94_310-88dup	XM_047418348.1:c.310-95_310-88dup	XM_047418348.1:c.310-96_310-88dup	XM_047418348.1:c.310-97_310-88dup	XM_047418348.1:c.310-88_310-87insGGGGGGGGGGG	XM_047418348.1:c.310-88_310-87insGGGGGGGGGGGG	XM_047418348.1:c.310-88_310-87insGGGGGGGGGGGGG	XM_047418348.1:c.310-88_310-87insGGGGGGGGGGGGGG	XM_047418348.1:c.310-88_310-87insGGGGGGGGGGGGGGG	XM_047418348.1:c.310-88_310-87insGGGGGGGGGGGGGGGG	XM_047418348.1:c.310-88_310-87insGGGGGGGGGGGGGGGGG

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#.

55 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77982251	Dec 07, 2007 (129)
2	HGSV	ss79886290	Dec 15, 2007 (130)
3	HGSV	ss83359255	Dec 15, 2007 (130)
4	HUMANGENOME_JCVI	ss95425604	Feb 06, 2009 (130)
5	BILGI_BIOE	ss666350581	Apr 25, 2013 (138)
6	1000GENOMES	ss1375374585	Aug 21, 2014 (142)
7	URBANLAB	ss3648328272	Oct 12, 2018 (152)
8	EVA_DECODE	ss3716991364	Jul 13, 2019 (153)
9	EVA_DECODE	ss3716991365	Jul 13, 2019 (153)
10	EVA_DECODE	ss3716991366	Jul 13, 2019 (153)
11	EVA_DECODE	ss3716991367	Jul 13, 2019 (153)
12	ACPOP	ss3733407082	Jul 13, 2019 (153)
13	ACPOP	ss3733407084	Jul 13, 2019 (153)
14	ACPOP	ss3733407085	Jul 13, 2019 (153)
15	PACBIO	ss3785444718	Jul 13, 2019 (153)
16	PACBIO	ss3790800651	Jul 13, 2019 (153)
17	PACBIO	ss3795679274	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3808034558	Jul 13, 2019 (153)
19	EVA	ss3829866485	Apr 26, 2020 (154)
20	GNOMAD	ss4139854506	Apr 26, 2021 (155)
21	GNOMAD	ss4139854511	Apr 26, 2021 (155)
22	GNOMAD	ss4139854512	Apr 26, 2021 (155)
23	GNOMAD	ss4139854513	Apr 26, 2021 (155)
24	GNOMAD	ss4139854514	Apr 26, 2021 (155)
25	GNOMAD	ss4139854515	Apr 26, 2021 (155)
26	GNOMAD	ss4139854516	Apr 26, 2021 (155)
27	GNOMAD	ss4139854517	Apr 26, 2021 (155)
28	GNOMAD	ss4139854518	Apr 26, 2021 (155)
29	GNOMAD	ss4139854519	Apr 26, 2021 (155)
30	GNOMAD	ss4139854520	Apr 26, 2021 (155)
31	GNOMAD	ss4139854521	Apr 26, 2021 (155)
32	GNOMAD	ss4139854522	Apr 26, 2021 (155)
33	GNOMAD	ss4139854523	Apr 26, 2021 (155)
34	GNOMAD	ss4139854524	Apr 26, 2021 (155)
35	GNOMAD	ss4139854525	Apr 26, 2021 (155)
36	GNOMAD	ss4139854526	Apr 26, 2021 (155)
37	GNOMAD	ss4139854530	Apr 26, 2021 (155)
38	GNOMAD	ss4139854531	Apr 26, 2021 (155)
39	EVA	ss5141923541	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5177013259	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5177013260	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5177013261	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5177013262	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5268056317	Oct 17, 2022 (156)
45	HUGCELL_USP	ss5465767151	Oct 17, 2022 (156)
46	HUGCELL_USP	ss5465767152	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5465767153	Oct 17, 2022 (156)
48	HUGCELL_USP	ss5465767154	Oct 17, 2022 (156)
49	TOMMO_GENOMICS	ss5714915504	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5714915505	Oct 17, 2022 (156)
51	TOMMO_GENOMICS	ss5714915508	Oct 17, 2022 (156)
52	EVA	ss5842088195	Oct 17, 2022 (156)
53	EVA	ss5842088196	Oct 17, 2022 (156)
54	EVA	ss5848656681	Oct 17, 2022 (156)
55	EVA	ss5935808459	Oct 17, 2022 (156)
56	1000Genomes	NC_000006.11 - 35706064	Oct 12, 2018 (152)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222035066 (NC_000006.12:35738286::G 2632/79366) Row 222035071 (NC_000006.12:35738286::GG 22403/78578) Row 222035072 (NC_000006.12:35738286::GGG 2854/79164)...	-	Apr 26, 2021 (155)
76	Northern Sweden Submission ignored due to conflicting rows: Row 6691947 (NC_000006.11:35706063::GG 180/544) Row 6691949 (NC_000006.11:35706063::G 8/544) Row 6691950 (NC_000006.11:35706063::GGG 15/544)	-	Jul 13, 2019 (153)
77	Northern Sweden Submission ignored due to conflicting rows: Row 6691947 (NC_000006.11:35706063::GG 180/544) Row 6691949 (NC_000006.11:35706063::G 8/544) Row 6691950 (NC_000006.11:35706063::GGG 15/544)	-	Jul 13, 2019 (153)
78	Northern Sweden Submission ignored due to conflicting rows: Row 6691947 (NC_000006.11:35706063::GG 180/544) Row 6691949 (NC_000006.11:35706063::G 8/544) Row 6691950 (NC_000006.11:35706063::GGG 15/544)	-	Jul 13, 2019 (153)
79	8.3KJPN Submission ignored due to conflicting rows: Row 34982566 (NC_000006.11:35706063::G 367/14746) Row 34982567 (NC_000006.11:35706063::GGG 170/14746) Row 34982568 (NC_000006.11:35706063::GG 2807/14746)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 34982566 (NC_000006.11:35706063::G 367/14746) Row 34982567 (NC_000006.11:35706063::GGG 170/14746) Row 34982568 (NC_000006.11:35706063::GG 2807/14746)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 34982566 (NC_000006.11:35706063::G 367/14746) Row 34982567 (NC_000006.11:35706063::GGG 170/14746) Row 34982568 (NC_000006.11:35706063::GG 2807/14746)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 34982566 (NC_000006.11:35706063::G 367/14746) Row 34982567 (NC_000006.11:35706063::GGG 170/14746) Row 34982568 (NC_000006.11:35706063::GG 2807/14746)...	-	Apr 26, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 48752608 (NC_000006.12:35738286::G 674/26864) Row 48752609 (NC_000006.12:35738286::GGG 353/26864) Row 48752612 (NC_000006.12:35738286::GG 5619/26864)	-	Oct 17, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 48752608 (NC_000006.12:35738286::G 674/26864) Row 48752609 (NC_000006.12:35738286::GGG 353/26864) Row 48752612 (NC_000006.12:35738286::GG 5619/26864)	-	Oct 17, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 48752608 (NC_000006.12:35738286::G 674/26864) Row 48752609 (NC_000006.12:35738286::GGG 353/26864) Row 48752612 (NC_000006.12:35738286::GG 5619/26864)	-	Oct 17, 2022 (156)
86	ALFA	NC_000006.12 - 35738287	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)
rs58642743	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4139854531	NC_000006.12:35738286:GG:	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGG	(self)
12327255253	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGG	(self)
31459804, ss1375374585, ss5935808459	NC_000006.11:35706063:G:	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGG	(self)
ss3808034558, ss4139854530, ss5141923541, ss5465767154	NC_000006.12:35738286:G:	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGG	(self)
12327255253	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGG	(self)
ss3733407084, ss5177013259	NC_000006.11:35706063::G	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss3716991367, ss4139854506, ss5465767152, ss5714915504	NC_000006.12:35738286::G	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGG	(self)
12327255253	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss77982251	NT_007592.15:35646073::G	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss666350581, ss3733407082, ss3785444718, ss3790800651, ss3795679274, ss3829866485, ss5177013261, ss5842088195	NC_000006.11:35706063::GG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGG	(self)
ss5848656681	NC_000006.11:35706073::GG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGG
ss3648328272, ss3716991366, ss4139854511, ss5268056317, ss5465767151, ss5714915508	NC_000006.12:35738286::GG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGG	(self)
12327255253	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGG	(self)
ss83359255, ss95425604	NT_007592.15:35646073::GG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3733407085, ss5177013260, ss5842088196	NC_000006.11:35706063::GGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss3716991365, ss4139854512, ss5465767153, ss5714915505	NC_000006.12:35738286::GGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGG	(self)
12327255253	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss79886290	NT_007592.15:35646073::GGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss5177013262	NC_000006.11:35706063::GGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss3716991364, ss4139854513	NC_000006.12:35738286::GGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGG	(self)
12327255253	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss4139854514	NC_000006.12:35738286::GGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
12327255253	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
ss4139854515	NC_000006.12:35738286::GGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss4139854516	NC_000006.12:35738286::GGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)
ss4139854517	NC_000006.12:35738286::GGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGG	(self)
ss4139854518	NC_000006.12:35738286::GGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGG	(self)
ss4139854519	NC_000006.12:35738286::GGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG	(self)
ss4139854520	NC_000006.12:35738286::GGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG	(self)
ss4139854521	NC_000006.12:35738286::GGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG	(self)
ss4139854522	NC_000006.12:35738286::GGGGGGGGGGG… NC_000006.12:35738286::GGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4139854523	NC_000006.12:35738286::GGGGGGGGGGG… NC_000006.12:35738286::GGGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4139854524	NC_000006.12:35738286::GGGGGGGGGGG… NC_000006.12:35738286::GGGGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4139854525	NC_000006.12:35738286::GGGGGGGGGGG… NC_000006.12:35738286::GGGGGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4139854526	NC_000006.12:35738286::GGGGGGGGGGG… NC_000006.12:35738286::GGGGGGGGGGGGGGGGG	NC_000006.12:35738286:GGGGGGGGGG:G… NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGG	(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 rs56101324

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs56101324