Name: rs10713074
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.

rs10713074

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:122422122-122422142 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₀ / del(T)₉ / del(T)₅ / del…
del(T)₁₀ / del(T)₉ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₁₁ / ins(T)₂₄
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.1513 (880/5816, ALFA)
delTT=0.4716 (2362/5008, 1000G)
delTT=0.4813 (1855/3854, ALSPAC) (+ 1 more)
delTT=0.4914 (1822/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADAD1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	5816	TTTTTTTTTTTTTTTTTTTTT=0.7503	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0906, TTTTTTTTTTTTTTTTTTTT=0.1513, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0046, TTTTTTTTTTTTTTTTTTTTTT=0.0022, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.766512	0.062684	0.170804	32
European	Sub	5392	TTTTTTTTTTTTTTTTTTTTT=0.7313	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0977, TTTTTTTTTTTTTTTTTTTT=0.1626, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0050, TTTTTTTTTTTTTTTTTTTTTT=0.0024, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.745035	0.068822	0.186143	32
African	Sub	172	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	166	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	20	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	12	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	146	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	66	TTTTTTTTTTTTTTTTTTTTT=0.95	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.05, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.909091	0.0	0.090909	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5816	(T)₂₁=0.7503	del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₅=0.0000, del(T)₄=0.0009, delTTT=0.0000, delTT=0.0906, delT=0.1513, dupT=0.0022, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0046
Allele Frequency Aggregator	European	Sub	5392	(T)₂₁=0.7313	del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₅=0.0000, del(T)₄=0.0009, delTTT=0.0000, delTT=0.0977, delT=0.1626, dupT=0.0024, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0050
Allele Frequency Aggregator	African	Sub	172	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₉=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	146	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₉=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	66	(T)₂₁=0.95	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.05, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	20	(T)₂₁=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₂₁=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(T)₂₁=1.0	del(T)₁₀=0.0, del(T)₉=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
1000Genomes	Global	Study-wide	5008	(T)₂₁=0.5284	delTT=0.4716
1000Genomes	African	Sub	1322	(T)₂₁=0.2814	delTT=0.7186
1000Genomes	East Asian	Sub	1008	(T)₂₁=0.6637	delTT=0.3363
1000Genomes	Europe	Sub	1006	(T)₂₁=0.5676	delTT=0.4324
1000Genomes	South Asian	Sub	978	(T)₂₁=0.556	delTT=0.444
1000Genomes	American	Sub	694	(T)₂₁=0.706	delTT=0.294
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₂₁=0.5187	delTT=0.4813
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₂₁=0.5086	delTT=0.4914

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 4	NC_000004.12:g.122422133_122422142del
GRCh38.p14 chr 4	NC_000004.12:g.122422134_122422142del
GRCh38.p14 chr 4	NC_000004.12:g.122422138_122422142del
GRCh38.p14 chr 4	NC_000004.12:g.122422139_122422142del
GRCh38.p14 chr 4	NC_000004.12:g.122422140_122422142del
GRCh38.p14 chr 4	NC_000004.12:g.122422141_122422142del
GRCh38.p14 chr 4	NC_000004.12:g.122422142del
GRCh38.p14 chr 4	NC_000004.12:g.122422142dup
GRCh38.p14 chr 4	NC_000004.12:g.122422141_122422142dup
GRCh38.p14 chr 4	NC_000004.12:g.122422140_122422142dup
GRCh38.p14 chr 4	NC_000004.12:g.122422139_122422142dup
GRCh38.p14 chr 4	NC_000004.12:g.122422138_122422142dup
GRCh38.p14 chr 4	NC_000004.12:g.122422132_122422142dup
GRCh38.p14 chr 4	NC_000004.12:g.122422142_122422143insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.123343288_123343297del
GRCh37.p13 chr 4	NC_000004.11:g.123343289_123343297del
GRCh37.p13 chr 4	NC_000004.11:g.123343293_123343297del
GRCh37.p13 chr 4	NC_000004.11:g.123343294_123343297del
GRCh37.p13 chr 4	NC_000004.11:g.123343295_123343297del
GRCh37.p13 chr 4	NC_000004.11:g.123343296_123343297del
GRCh37.p13 chr 4	NC_000004.11:g.123343297del
GRCh37.p13 chr 4	NC_000004.11:g.123343297dup
GRCh37.p13 chr 4	NC_000004.11:g.123343296_123343297dup
GRCh37.p13 chr 4	NC_000004.11:g.123343295_123343297dup
GRCh37.p13 chr 4	NC_000004.11:g.123343294_123343297dup
GRCh37.p13 chr 4	NC_000004.11:g.123343293_123343297dup
GRCh37.p13 chr 4	NC_000004.11:g.123343287_123343297dup
GRCh37.p13 chr 4	NC_000004.11:g.123343297_123343298insTTTTTTTTTTTTTTTTTTTTTTTT

Gene: ADAD1, adenosine deaminase domain containing 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ADAD1 transcript variant 2	NM_001159285.2:c.1584+743… NM_001159285.2:c.1584+743_1584+752del	N/A	Intron Variant
ADAD1 transcript variant 3	NM_001159295.2:c.1563+743… NM_001159295.2:c.1563+743_1563+752del	N/A	Intron Variant
ADAD1 transcript variant 1	NM_139243.4:c.1617+743_16… NM_139243.4:c.1617+743_1617+752del	N/A	Intron Variant
ADAD1 transcript variant X1	XM_005262741.3:c.1617+743… XM_005262741.3:c.1617+743_1617+752del	N/A	Intron Variant
ADAD1 transcript variant X4	XM_005262743.4:c.1617+743… XM_005262743.4:c.1617+743_1617+752del	N/A	Intron Variant
ADAD1 transcript variant X5	XM_005262744.4:c.1584+743… XM_005262744.4:c.1584+743_1584+752del	N/A	Intron Variant
ADAD1 transcript variant X7	XM_005262745.4:c.1548+743… XM_005262745.4:c.1548+743_1548+752del	N/A	Intron Variant
ADAD1 transcript variant X3	XM_011531603.3:c.1617+743… XM_011531603.3:c.1617+743_1617+752del	N/A	Intron Variant
ADAD1 transcript variant X2	XM_024453888.1:c.1617+743… XM_024453888.1:c.1617+743_1617+752del	N/A	Intron Variant
ADAD1 transcript variant X6	XM_024453889.1:c.1584+743… XM_024453889.1:c.1584+743_1584+752del	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	(T)₂₁=	del(T)₁₀	del(T)₉	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₁₁	ins(T)₂₄
GRCh38.p14 chr 4	NC_000004.12:g.122422122_122422142=	NC_000004.12:g.122422133_122422142del	NC_000004.12:g.122422134_122422142del	NC_000004.12:g.122422138_122422142del	NC_000004.12:g.122422139_122422142del	NC_000004.12:g.122422140_122422142del	NC_000004.12:g.122422141_122422142del	NC_000004.12:g.122422142del	NC_000004.12:g.122422142dup	NC_000004.12:g.122422141_122422142dup	NC_000004.12:g.122422140_122422142dup	NC_000004.12:g.122422139_122422142dup	NC_000004.12:g.122422138_122422142dup	NC_000004.12:g.122422132_122422142dup	NC_000004.12:g.122422142_122422143insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.123343277_123343297=	NC_000004.11:g.123343288_123343297del	NC_000004.11:g.123343289_123343297del	NC_000004.11:g.123343293_123343297del	NC_000004.11:g.123343294_123343297del	NC_000004.11:g.123343295_123343297del	NC_000004.11:g.123343296_123343297del	NC_000004.11:g.123343297del	NC_000004.11:g.123343297dup	NC_000004.11:g.123343296_123343297dup	NC_000004.11:g.123343295_123343297dup	NC_000004.11:g.123343294_123343297dup	NC_000004.11:g.123343293_123343297dup	NC_000004.11:g.123343287_123343297dup	NC_000004.11:g.123343297_123343298insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant 2	NM_001159285.1:c.1584+732=	NM_001159285.1:c.1584+743_1584+752del	NM_001159285.1:c.1584+744_1584+752del	NM_001159285.1:c.1584+748_1584+752del	NM_001159285.1:c.1584+749_1584+752del	NM_001159285.1:c.1584+750_1584+752del	NM_001159285.1:c.1584+751_1584+752del	NM_001159285.1:c.1584+752del	NM_001159285.1:c.1584+752dup	NM_001159285.1:c.1584+751_1584+752dup	NM_001159285.1:c.1584+750_1584+752dup	NM_001159285.1:c.1584+749_1584+752dup	NM_001159285.1:c.1584+748_1584+752dup	NM_001159285.1:c.1584+742_1584+752dup	NM_001159285.1:c.1584+752_1584+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant 2	NM_001159285.2:c.1584+732=	NM_001159285.2:c.1584+743_1584+752del	NM_001159285.2:c.1584+744_1584+752del	NM_001159285.2:c.1584+748_1584+752del	NM_001159285.2:c.1584+749_1584+752del	NM_001159285.2:c.1584+750_1584+752del	NM_001159285.2:c.1584+751_1584+752del	NM_001159285.2:c.1584+752del	NM_001159285.2:c.1584+752dup	NM_001159285.2:c.1584+751_1584+752dup	NM_001159285.2:c.1584+750_1584+752dup	NM_001159285.2:c.1584+749_1584+752dup	NM_001159285.2:c.1584+748_1584+752dup	NM_001159285.2:c.1584+742_1584+752dup	NM_001159285.2:c.1584+752_1584+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant 3	NM_001159295.1:c.1563+732=	NM_001159295.1:c.1563+743_1563+752del	NM_001159295.1:c.1563+744_1563+752del	NM_001159295.1:c.1563+748_1563+752del	NM_001159295.1:c.1563+749_1563+752del	NM_001159295.1:c.1563+750_1563+752del	NM_001159295.1:c.1563+751_1563+752del	NM_001159295.1:c.1563+752del	NM_001159295.1:c.1563+752dup	NM_001159295.1:c.1563+751_1563+752dup	NM_001159295.1:c.1563+750_1563+752dup	NM_001159295.1:c.1563+749_1563+752dup	NM_001159295.1:c.1563+748_1563+752dup	NM_001159295.1:c.1563+742_1563+752dup	NM_001159295.1:c.1563+752_1563+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant 3	NM_001159295.2:c.1563+732=	NM_001159295.2:c.1563+743_1563+752del	NM_001159295.2:c.1563+744_1563+752del	NM_001159295.2:c.1563+748_1563+752del	NM_001159295.2:c.1563+749_1563+752del	NM_001159295.2:c.1563+750_1563+752del	NM_001159295.2:c.1563+751_1563+752del	NM_001159295.2:c.1563+752del	NM_001159295.2:c.1563+752dup	NM_001159295.2:c.1563+751_1563+752dup	NM_001159295.2:c.1563+750_1563+752dup	NM_001159295.2:c.1563+749_1563+752dup	NM_001159295.2:c.1563+748_1563+752dup	NM_001159295.2:c.1563+742_1563+752dup	NM_001159295.2:c.1563+752_1563+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant 1	NM_139243.3:c.1617+732=	NM_139243.3:c.1617+743_1617+752del	NM_139243.3:c.1617+744_1617+752del	NM_139243.3:c.1617+748_1617+752del	NM_139243.3:c.1617+749_1617+752del	NM_139243.3:c.1617+750_1617+752del	NM_139243.3:c.1617+751_1617+752del	NM_139243.3:c.1617+752del	NM_139243.3:c.1617+752dup	NM_139243.3:c.1617+751_1617+752dup	NM_139243.3:c.1617+750_1617+752dup	NM_139243.3:c.1617+749_1617+752dup	NM_139243.3:c.1617+748_1617+752dup	NM_139243.3:c.1617+742_1617+752dup	NM_139243.3:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant 1	NM_139243.4:c.1617+732=	NM_139243.4:c.1617+743_1617+752del	NM_139243.4:c.1617+744_1617+752del	NM_139243.4:c.1617+748_1617+752del	NM_139243.4:c.1617+749_1617+752del	NM_139243.4:c.1617+750_1617+752del	NM_139243.4:c.1617+751_1617+752del	NM_139243.4:c.1617+752del	NM_139243.4:c.1617+752dup	NM_139243.4:c.1617+751_1617+752dup	NM_139243.4:c.1617+750_1617+752dup	NM_139243.4:c.1617+749_1617+752dup	NM_139243.4:c.1617+748_1617+752dup	NM_139243.4:c.1617+742_1617+752dup	NM_139243.4:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X1	XM_005262741.1:c.1617+732=	XM_005262741.1:c.1617+743_1617+752del	XM_005262741.1:c.1617+744_1617+752del	XM_005262741.1:c.1617+748_1617+752del	XM_005262741.1:c.1617+749_1617+752del	XM_005262741.1:c.1617+750_1617+752del	XM_005262741.1:c.1617+751_1617+752del	XM_005262741.1:c.1617+752del	XM_005262741.1:c.1617+752dup	XM_005262741.1:c.1617+751_1617+752dup	XM_005262741.1:c.1617+750_1617+752dup	XM_005262741.1:c.1617+749_1617+752dup	XM_005262741.1:c.1617+748_1617+752dup	XM_005262741.1:c.1617+742_1617+752dup	XM_005262741.1:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X1	XM_005262741.3:c.1617+732=	XM_005262741.3:c.1617+743_1617+752del	XM_005262741.3:c.1617+744_1617+752del	XM_005262741.3:c.1617+748_1617+752del	XM_005262741.3:c.1617+749_1617+752del	XM_005262741.3:c.1617+750_1617+752del	XM_005262741.3:c.1617+751_1617+752del	XM_005262741.3:c.1617+752del	XM_005262741.3:c.1617+752dup	XM_005262741.3:c.1617+751_1617+752dup	XM_005262741.3:c.1617+750_1617+752dup	XM_005262741.3:c.1617+749_1617+752dup	XM_005262741.3:c.1617+748_1617+752dup	XM_005262741.3:c.1617+742_1617+752dup	XM_005262741.3:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X2	XM_005262742.1:c.1617+732=	XM_005262742.1:c.1617+743_1617+752del	XM_005262742.1:c.1617+744_1617+752del	XM_005262742.1:c.1617+748_1617+752del	XM_005262742.1:c.1617+749_1617+752del	XM_005262742.1:c.1617+750_1617+752del	XM_005262742.1:c.1617+751_1617+752del	XM_005262742.1:c.1617+752del	XM_005262742.1:c.1617+752dup	XM_005262742.1:c.1617+751_1617+752dup	XM_005262742.1:c.1617+750_1617+752dup	XM_005262742.1:c.1617+749_1617+752dup	XM_005262742.1:c.1617+748_1617+752dup	XM_005262742.1:c.1617+742_1617+752dup	XM_005262742.1:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X3	XM_005262743.1:c.1617+732=	XM_005262743.1:c.1617+743_1617+752del	XM_005262743.1:c.1617+744_1617+752del	XM_005262743.1:c.1617+748_1617+752del	XM_005262743.1:c.1617+749_1617+752del	XM_005262743.1:c.1617+750_1617+752del	XM_005262743.1:c.1617+751_1617+752del	XM_005262743.1:c.1617+752del	XM_005262743.1:c.1617+752dup	XM_005262743.1:c.1617+751_1617+752dup	XM_005262743.1:c.1617+750_1617+752dup	XM_005262743.1:c.1617+749_1617+752dup	XM_005262743.1:c.1617+748_1617+752dup	XM_005262743.1:c.1617+742_1617+752dup	XM_005262743.1:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X4	XM_005262743.4:c.1617+732=	XM_005262743.4:c.1617+743_1617+752del	XM_005262743.4:c.1617+744_1617+752del	XM_005262743.4:c.1617+748_1617+752del	XM_005262743.4:c.1617+749_1617+752del	XM_005262743.4:c.1617+750_1617+752del	XM_005262743.4:c.1617+751_1617+752del	XM_005262743.4:c.1617+752del	XM_005262743.4:c.1617+752dup	XM_005262743.4:c.1617+751_1617+752dup	XM_005262743.4:c.1617+750_1617+752dup	XM_005262743.4:c.1617+749_1617+752dup	XM_005262743.4:c.1617+748_1617+752dup	XM_005262743.4:c.1617+742_1617+752dup	XM_005262743.4:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X4	XM_005262744.1:c.1584+732=	XM_005262744.1:c.1584+743_1584+752del	XM_005262744.1:c.1584+744_1584+752del	XM_005262744.1:c.1584+748_1584+752del	XM_005262744.1:c.1584+749_1584+752del	XM_005262744.1:c.1584+750_1584+752del	XM_005262744.1:c.1584+751_1584+752del	XM_005262744.1:c.1584+752del	XM_005262744.1:c.1584+752dup	XM_005262744.1:c.1584+751_1584+752dup	XM_005262744.1:c.1584+750_1584+752dup	XM_005262744.1:c.1584+749_1584+752dup	XM_005262744.1:c.1584+748_1584+752dup	XM_005262744.1:c.1584+742_1584+752dup	XM_005262744.1:c.1584+752_1584+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X5	XM_005262744.4:c.1584+732=	XM_005262744.4:c.1584+743_1584+752del	XM_005262744.4:c.1584+744_1584+752del	XM_005262744.4:c.1584+748_1584+752del	XM_005262744.4:c.1584+749_1584+752del	XM_005262744.4:c.1584+750_1584+752del	XM_005262744.4:c.1584+751_1584+752del	XM_005262744.4:c.1584+752del	XM_005262744.4:c.1584+752dup	XM_005262744.4:c.1584+751_1584+752dup	XM_005262744.4:c.1584+750_1584+752dup	XM_005262744.4:c.1584+749_1584+752dup	XM_005262744.4:c.1584+748_1584+752dup	XM_005262744.4:c.1584+742_1584+752dup	XM_005262744.4:c.1584+752_1584+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X5	XM_005262745.1:c.1548+732=	XM_005262745.1:c.1548+743_1548+752del	XM_005262745.1:c.1548+744_1548+752del	XM_005262745.1:c.1548+748_1548+752del	XM_005262745.1:c.1548+749_1548+752del	XM_005262745.1:c.1548+750_1548+752del	XM_005262745.1:c.1548+751_1548+752del	XM_005262745.1:c.1548+752del	XM_005262745.1:c.1548+752dup	XM_005262745.1:c.1548+751_1548+752dup	XM_005262745.1:c.1548+750_1548+752dup	XM_005262745.1:c.1548+749_1548+752dup	XM_005262745.1:c.1548+748_1548+752dup	XM_005262745.1:c.1548+742_1548+752dup	XM_005262745.1:c.1548+752_1548+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X7	XM_005262745.4:c.1548+732=	XM_005262745.4:c.1548+743_1548+752del	XM_005262745.4:c.1548+744_1548+752del	XM_005262745.4:c.1548+748_1548+752del	XM_005262745.4:c.1548+749_1548+752del	XM_005262745.4:c.1548+750_1548+752del	XM_005262745.4:c.1548+751_1548+752del	XM_005262745.4:c.1548+752del	XM_005262745.4:c.1548+752dup	XM_005262745.4:c.1548+751_1548+752dup	XM_005262745.4:c.1548+750_1548+752dup	XM_005262745.4:c.1548+749_1548+752dup	XM_005262745.4:c.1548+748_1548+752dup	XM_005262745.4:c.1548+742_1548+752dup	XM_005262745.4:c.1548+752_1548+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X3	XM_011531603.3:c.1617+732=	XM_011531603.3:c.1617+743_1617+752del	XM_011531603.3:c.1617+744_1617+752del	XM_011531603.3:c.1617+748_1617+752del	XM_011531603.3:c.1617+749_1617+752del	XM_011531603.3:c.1617+750_1617+752del	XM_011531603.3:c.1617+751_1617+752del	XM_011531603.3:c.1617+752del	XM_011531603.3:c.1617+752dup	XM_011531603.3:c.1617+751_1617+752dup	XM_011531603.3:c.1617+750_1617+752dup	XM_011531603.3:c.1617+749_1617+752dup	XM_011531603.3:c.1617+748_1617+752dup	XM_011531603.3:c.1617+742_1617+752dup	XM_011531603.3:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X2	XM_024453888.1:c.1617+732=	XM_024453888.1:c.1617+743_1617+752del	XM_024453888.1:c.1617+744_1617+752del	XM_024453888.1:c.1617+748_1617+752del	XM_024453888.1:c.1617+749_1617+752del	XM_024453888.1:c.1617+750_1617+752del	XM_024453888.1:c.1617+751_1617+752del	XM_024453888.1:c.1617+752del	XM_024453888.1:c.1617+752dup	XM_024453888.1:c.1617+751_1617+752dup	XM_024453888.1:c.1617+750_1617+752dup	XM_024453888.1:c.1617+749_1617+752dup	XM_024453888.1:c.1617+748_1617+752dup	XM_024453888.1:c.1617+742_1617+752dup	XM_024453888.1:c.1617+752_1617+753insTTTTTTTTTTTTTTTTTTTTTTTT
ADAD1 transcript variant X6	XM_024453889.1:c.1584+732=	XM_024453889.1:c.1584+743_1584+752del	XM_024453889.1:c.1584+744_1584+752del	XM_024453889.1:c.1584+748_1584+752del	XM_024453889.1:c.1584+749_1584+752del	XM_024453889.1:c.1584+750_1584+752del	XM_024453889.1:c.1584+751_1584+752del	XM_024453889.1:c.1584+752del	XM_024453889.1:c.1584+752dup	XM_024453889.1:c.1584+751_1584+752dup	XM_024453889.1:c.1584+750_1584+752dup	XM_024453889.1:c.1584+749_1584+752dup	XM_024453889.1:c.1584+748_1584+752dup	XM_024453889.1:c.1584+742_1584+752dup	XM_024453889.1:c.1584+752_1584+753insTTTTTTTTTTTTTTTTTTTTTTTT

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#.

54 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77972527	Dec 07, 2007 (135)
2	HGSV	ss83852671	Aug 21, 2014 (142)
3	HUMANGENOME_JCVI	ss95367842	Dec 05, 2013 (138)
4	PJP	ss295185947	Jan 10, 2018 (151)
5	1000GENOMES	ss1372733280	Jan 10, 2018 (151)
6	EVA_UK10K_ALSPAC	ss1704338773	Jan 10, 2018 (151)
7	EVA_UK10K_TWINSUK	ss1704339434	Jan 10, 2018 (151)
8	SWEGEN	ss2995471206	Nov 08, 2017 (151)
9	EVA_DECODE	ss3712964625	Jul 13, 2019 (153)
10	EVA_DECODE	ss3712964627	Jul 13, 2019 (153)
11	EVA_DECODE	ss3712964628	Jul 13, 2019 (153)
12	EVA_DECODE	ss3712964629	Jul 13, 2019 (153)
13	PACBIO	ss3784845849	Jul 13, 2019 (153)
14	PACBIO	ss3790283898	Jul 13, 2019 (153)
15	PACBIO	ss3790283899	Jul 13, 2019 (153)
16	PACBIO	ss3795159360	Jul 13, 2019 (153)
17	PACBIO	ss3795159361	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3805505629	Jul 13, 2019 (153)
19	EVA	ss3828783258	Apr 26, 2020 (154)
20	KOGIC	ss3955026961	Apr 26, 2020 (154)
21	KOGIC	ss3955026962	Apr 26, 2020 (154)
22	KOGIC	ss3955026963	Apr 26, 2020 (154)
23	KOGIC	ss3955026964	Apr 26, 2020 (154)
24	GNOMAD	ss4119516544	Apr 26, 2021 (155)
25	GNOMAD	ss4119516548	Apr 26, 2021 (155)
26	GNOMAD	ss4119516549	Apr 26, 2021 (155)
27	GNOMAD	ss4119516550	Apr 26, 2021 (155)
28	GNOMAD	ss4119516551	Apr 26, 2021 (155)
29	GNOMAD	ss4119516552	Apr 26, 2021 (155)
30	GNOMAD	ss4119516553	Apr 26, 2021 (155)
31	GNOMAD	ss4119516554	Apr 26, 2021 (155)
32	GNOMAD	ss4119516555	Apr 26, 2021 (155)
33	GNOMAD	ss4119516556	Apr 26, 2021 (155)
34	GNOMAD	ss4119516557	Apr 26, 2021 (155)
35	GNOMAD	ss4119516558	Apr 26, 2021 (155)
36	GNOMAD	ss4119516559	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5167774409	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5167774410	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5167774411	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5260842459	Oct 17, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5260842460	Oct 17, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5260842461	Oct 17, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5260842462	Oct 17, 2022 (156)
44	HUGCELL_USP	ss5459419396	Oct 17, 2022 (156)
45	HUGCELL_USP	ss5459419397	Oct 17, 2022 (156)
46	HUGCELL_USP	ss5459419398	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5459419399	Oct 17, 2022 (156)
48	HUGCELL_USP	ss5459419400	Oct 17, 2022 (156)
49	TOMMO_GENOMICS	ss5702701560	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5702701561	Oct 17, 2022 (156)
51	TOMMO_GENOMICS	ss5702701562	Oct 17, 2022 (156)
52	EVA	ss5844641032	Oct 17, 2022 (156)
53	EVA	ss5844641033	Oct 17, 2022 (156)
54	EVA	ss5854421193	Oct 17, 2022 (156)
55	1000Genomes	NC_000004.11 - 123343277	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 123343277	Oct 12, 2018 (152)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 163472167 (NC_000004.12:122422121::T 426/103692) Row 163472175 (NC_000004.12:122422121::TT 642/103696) Row 163472176 (NC_000004.12:122422121::TTT 33/103720)...	-	Apr 26, 2021 (155)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 11404962 (NC_000004.12:122422123:T: 564/1816) Row 11404963 (NC_000004.12:122422124::T 106/1816) Row 11404964 (NC_000004.12:122422122:TT: 219/1816)...	-	Apr 26, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 11404962 (NC_000004.12:122422123:T: 564/1816) Row 11404963 (NC_000004.12:122422124::T 106/1816) Row 11404964 (NC_000004.12:122422122:TT: 219/1816)...	-	Apr 26, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 11404962 (NC_000004.12:122422123:T: 564/1816) Row 11404963 (NC_000004.12:122422124::T 106/1816) Row 11404964 (NC_000004.12:122422122:TT: 219/1816)...	-	Apr 26, 2020 (154)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 11404962 (NC_000004.12:122422123:T: 564/1816) Row 11404963 (NC_000004.12:122422124::T 106/1816) Row 11404964 (NC_000004.12:122422122:TT: 219/1816)...	-	Apr 26, 2020 (154)
74	8.3KJPN Submission ignored due to conflicting rows: Row 25743716 (NC_000004.11:123343276:T: 4889/16652) Row 25743717 (NC_000004.11:123343276:TT: 1969/16652) Row 25743718 (NC_000004.11:123343276::T 43/16652)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 25743716 (NC_000004.11:123343276:T: 4889/16652) Row 25743717 (NC_000004.11:123343276:TT: 1969/16652) Row 25743718 (NC_000004.11:123343276::T 43/16652)	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 25743716 (NC_000004.11:123343276:T: 4889/16652) Row 25743717 (NC_000004.11:123343276:TT: 1969/16652) Row 25743718 (NC_000004.11:123343276::T 43/16652)	-	Apr 26, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 36538664 (NC_000004.12:122422121:T: 8907/28232) Row 36538665 (NC_000004.12:122422121:TT: 3878/28232) Row 36538666 (NC_000004.12:122422121::T 83/28232)	-	Oct 17, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 36538664 (NC_000004.12:122422121:T: 8907/28232) Row 36538665 (NC_000004.12:122422121:TT: 3878/28232) Row 36538666 (NC_000004.12:122422121::T 83/28232)	-	Oct 17, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 36538664 (NC_000004.12:122422121:T: 8907/28232) Row 36538665 (NC_000004.12:122422121:TT: 3878/28232) Row 36538666 (NC_000004.12:122422121::T 83/28232)	-	Oct 17, 2022 (156)
80	UK 10K study - Twins	NC_000004.11 - 123343277	Oct 12, 2018 (152)
81	ALFA	NC_000004.12 - 122422122	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)
rs56172758	Oct 06, 2011 (135)
rs57550742	Oct 06, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4119516559	NC_000004.12:122422121:TTTTTTTTTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4119516558	NC_000004.12:122422121:TTTTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss83852671	NC_000004.9:123700898:TTTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss2995471206	NC_000004.11:123343276:TTTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3712964625, ss4119516557, ss5260842462, ss5459419399	NC_000004.12:122422121:TTTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5844641033	NC_000004.11:123343276:TTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
ss3955026964, ss4119516556, ss5260842461, ss5459419398	NC_000004.12:122422121:TTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3712964627	NC_000004.12:122422122:TTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss77972527	NC_000004.9:123700900:TT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss295185947	NC_000004.10:123562726:TT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
23076880, 12838770, 12838770, ss1372733280, ss1704338773, ss1704339434, ss3790283898, ss3795159360, ss5167774410, ss5844641032	NC_000004.11:123343276:TT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3805505629, ss4119516555, ss5260842459, ss5459419396, ss5702701561	NC_000004.12:122422121:TT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3955026963	NC_000004.12:122422122:TT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3712964628	NC_000004.12:122422123:TT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3784845849, ss3790283899, ss3795159361, ss3828783258, ss5167774409	NC_000004.11:123343276:T:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4119516554, ss5260842460, ss5459419397, ss5702701560, ss5854421193	NC_000004.12:122422121:T:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3955026961	NC_000004.12:122422123:T:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3712964629	NC_000004.12:122422124:T:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss95367842	NT_016354.19:47891017:T:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5167774411	NC_000004.11:123343276::T	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4119516544, ss5459419400, ss5702701562	NC_000004.12:122422121::T	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3955026962	NC_000004.12:122422124::T	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss95367842	NT_016354.19:47891017:T:TT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4119516548	NC_000004.12:122422121::TT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4119516549	NC_000004.12:122422121::TTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4119516550	NC_000004.12:122422121::TTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
851056157	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4119516551	NC_000004.12:122422121::TTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4119516552	NC_000004.12:122422121::TTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4119516553	NC_000004.12:122422121::TTTTTTTTTT… NC_000004.12:122422121::TTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3441416656	NC_000004.12:122422121:TTTTTTTTT:	NC_000004.12:122422121:TTTTTTTTTTT… NC_000004.12:122422121:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT

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

No publications for rs10713074

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

rs10713074