Name: rs1210367064
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.

rs1210367064

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:149263325-149263334 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇
Variation Type: Indel Insertion and Deletion
Frequency: dup(T)₇=0.000004 (1/264690, TOPMED)
del(T)₄=0.00000 (0/11820, ALFA)
delTTT=0.00000 (0/11820, ALFA) (+ 10 more)
delTT=0.00000 (0/11820, ALFA)
delT=0.00000 (0/11820, ALFA)
dupT=0.00000 (0/11820, ALFA)
dupTT=0.00000 (0/11820, ALFA)
dupTTT=0.00000 (0/11820, ALFA)
dup(T)₄=0.00000 (0/11820, ALFA)
dup(T)₅=0.00000 (0/11820, ALFA)
dup(T)₆=0.00000 (0/11820, ALFA)
dup(T)₇=0.00000 (0/11820, ALFA)
dupTT=0.010 (6/592, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF783 : Intron Variant
LOC124901769 : 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	11820	TTTTTTTTTT=1.00000	TTTTTT=0.00000, TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7604	TTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2798	TTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	108	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African American	Sub	2690	TTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	106	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	82	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	24	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	146	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	610	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	94	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	462	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	- No frequency provided	dup(T)₇=0.000004
Allele Frequency Aggregator	Total	Global	11820	(T)₁₀=1.00000	del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	European	Sub	7604	(T)₁₀=1.0000	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	African	Sub	2798	(T)₁₀=1.0000	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	(T)₁₀=1.000	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, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	462	(T)₁₀=1.000	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, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(T)₁₀=1.000	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, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Asian	Sub	106	(T)₁₀=1.000	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, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(T)₁₀=1.00	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, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Northern Sweden	ACPOP	Study-wide	592	- No frequency provided	dupTT=0.010

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 7	NC_000007.14:g.149263331_149263334del
GRCh38.p14 chr 7	NC_000007.14:g.149263332_149263334del
GRCh38.p14 chr 7	NC_000007.14:g.149263333_149263334del
GRCh38.p14 chr 7	NC_000007.14:g.149263334del
GRCh38.p14 chr 7	NC_000007.14:g.149263334dup
GRCh38.p14 chr 7	NC_000007.14:g.149263333_149263334dup
GRCh38.p14 chr 7	NC_000007.14:g.149263332_149263334dup
GRCh38.p14 chr 7	NC_000007.14:g.149263331_149263334dup
GRCh38.p14 chr 7	NC_000007.14:g.149263330_149263334dup
GRCh38.p14 chr 7	NC_000007.14:g.149263329_149263334dup
GRCh38.p14 chr 7	NC_000007.14:g.149263328_149263334dup
GRCh37.p13 chr 7	NC_000007.13:g.148960422_148960425del
GRCh37.p13 chr 7	NC_000007.13:g.148960423_148960425del
GRCh37.p13 chr 7	NC_000007.13:g.148960424_148960425del
GRCh37.p13 chr 7	NC_000007.13:g.148960425del
GRCh37.p13 chr 7	NC_000007.13:g.148960425dup
GRCh37.p13 chr 7	NC_000007.13:g.148960424_148960425dup
GRCh37.p13 chr 7	NC_000007.13:g.148960423_148960425dup
GRCh37.p13 chr 7	NC_000007.13:g.148960422_148960425dup
GRCh37.p13 chr 7	NC_000007.13:g.148960421_148960425dup
GRCh37.p13 chr 7	NC_000007.13:g.148960420_148960425dup
GRCh37.p13 chr 7	NC_000007.13:g.148960419_148960425dup

Gene: ZNF783, zinc finger protein 783 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF783 transcript variant 1	NM_001195220.2:c.24+974_2… NM_001195220.2:c.24+974_24+977del	N/A	Intron Variant
ZNF783 transcript variant 2	NR_144366.2:n.	N/A	Intron Variant
ZNF783 transcript variant 3	NR_144367.1:n.	N/A	Genic Upstream Transcript Variant
ZNF783 transcript variant X2	XM_047419692.1:c.-1675_-1… XM_047419692.1:c.-1675_-1666=	N/A	5 Prime UTR Variant
ZNF783 transcript variant X1	XM_011515701.3:c.	N/A	Genic Upstream Transcript Variant
ZNF783 transcript variant X3	XR_001744503.2:n.	N/A	Genic Upstream Transcript Variant

Gene: LOC124901769, uncharacterized LOC124901769 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124901769 transcript	XR_007060582.1: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	(T)₁₀=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇
GRCh38.p14 chr 7	NC_000007.14:g.149263325_149263334=	NC_000007.14:g.149263331_149263334del	NC_000007.14:g.149263332_149263334del	NC_000007.14:g.149263333_149263334del	NC_000007.14:g.149263334del	NC_000007.14:g.149263334dup	NC_000007.14:g.149263333_149263334dup	NC_000007.14:g.149263332_149263334dup	NC_000007.14:g.149263331_149263334dup	NC_000007.14:g.149263330_149263334dup	NC_000007.14:g.149263329_149263334dup	NC_000007.14:g.149263328_149263334dup
GRCh37.p13 chr 7	NC_000007.13:g.148960416_148960425=	NC_000007.13:g.148960422_148960425del	NC_000007.13:g.148960423_148960425del	NC_000007.13:g.148960424_148960425del	NC_000007.13:g.148960425del	NC_000007.13:g.148960425dup	NC_000007.13:g.148960424_148960425dup	NC_000007.13:g.148960423_148960425dup	NC_000007.13:g.148960422_148960425dup	NC_000007.13:g.148960421_148960425dup	NC_000007.13:g.148960420_148960425dup	NC_000007.13:g.148960419_148960425dup
ZNF783 transcript variant X2	XM_047419692.1:c.-1675_-1666=	XM_047419692.1:c.-1669_-1666del	XM_047419692.1:c.-1668_-1666del	XM_047419692.1:c.-1667_-1666del	XM_047419692.1:c.-1666del	XM_047419692.1:c.-1666dup	XM_047419692.1:c.-1667_-1666dup	XM_047419692.1:c.-1668_-1666dup	XM_047419692.1:c.-1669_-1666dup	XM_047419692.1:c.-1670_-1666dup	XM_047419692.1:c.-1671_-1666dup	XM_047419692.1:c.-1672_-1666dup
ZNF783 transcript variant 1	NM_001195220.1:c.24+968=	NM_001195220.1:c.24+974_24+977del	NM_001195220.1:c.24+975_24+977del	NM_001195220.1:c.24+976_24+977del	NM_001195220.1:c.24+977del	NM_001195220.1:c.24+977dup	NM_001195220.1:c.24+976_24+977dup	NM_001195220.1:c.24+975_24+977dup	NM_001195220.1:c.24+974_24+977dup	NM_001195220.1:c.24+973_24+977dup	NM_001195220.1:c.24+972_24+977dup	NM_001195220.1:c.24+971_24+977dup
ZNF783 transcript variant 1	NM_001195220.2:c.24+968=	NM_001195220.2:c.24+974_24+977del	NM_001195220.2:c.24+975_24+977del	NM_001195220.2:c.24+976_24+977del	NM_001195220.2:c.24+977del	NM_001195220.2:c.24+977dup	NM_001195220.2:c.24+976_24+977dup	NM_001195220.2:c.24+975_24+977dup	NM_001195220.2:c.24+974_24+977dup	NM_001195220.2:c.24+973_24+977dup	NM_001195220.2:c.24+972_24+977dup	NM_001195220.2:c.24+971_24+977dup
ZNF783 transcript variant X1	XM_005249929.1:c.24+968=	XM_005249929.1:c.24+974_24+977del	XM_005249929.1:c.24+975_24+977del	XM_005249929.1:c.24+976_24+977del	XM_005249929.1:c.24+977del	XM_005249929.1:c.24+977dup	XM_005249929.1:c.24+976_24+977dup	XM_005249929.1:c.24+975_24+977dup	XM_005249929.1:c.24+974_24+977dup	XM_005249929.1:c.24+973_24+977dup	XM_005249929.1:c.24+972_24+977dup	XM_005249929.1:c.24+971_24+977dup
ZNF783 transcript variant X2	XM_005249930.1:c.24+968=	XM_005249930.1:c.24+974_24+977del	XM_005249930.1:c.24+975_24+977del	XM_005249930.1:c.24+976_24+977del	XM_005249930.1:c.24+977del	XM_005249930.1:c.24+977dup	XM_005249930.1:c.24+976_24+977dup	XM_005249930.1:c.24+975_24+977dup	XM_005249930.1:c.24+974_24+977dup	XM_005249930.1:c.24+973_24+977dup	XM_005249930.1:c.24+972_24+977dup	XM_005249930.1:c.24+971_24+977dup

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#.

29 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3720968446	Jul 13, 2019 (153)
2	EVA_DECODE	ss3720968449	Jul 13, 2019 (153)
3	EVA_DECODE	ss3720968450	Jul 13, 2019 (153)
4	EVA_DECODE	ss3720968451	Jul 13, 2019 (153)
5	ACPOP	ss3735191816	Jul 13, 2019 (153)
6	KOGIC	ss3962844653	Apr 26, 2020 (154)
7	KOGIC	ss3962844654	Apr 26, 2020 (154)
8	KOGIC	ss3962844655	Apr 26, 2020 (154)
9	KOGIC	ss3962844656	Apr 26, 2020 (154)
10	GNOMAD	ss4175571232	Apr 26, 2021 (155)
11	GNOMAD	ss4175571235	Apr 26, 2021 (155)
12	GNOMAD	ss4175571236	Apr 26, 2021 (155)
13	GNOMAD	ss4175571237	Apr 26, 2021 (155)
14	GNOMAD	ss4175571238	Apr 26, 2021 (155)
15	GNOMAD	ss4175571239	Apr 26, 2021 (155)
16	GNOMAD	ss4175571240	Apr 26, 2021 (155)
17	GNOMAD	ss4175571241	Apr 26, 2021 (155)
18	GNOMAD	ss4175571242	Apr 26, 2021 (155)
19	GNOMAD	ss4175571243	Apr 26, 2021 (155)
20	TOPMED	ss4768567295	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5186222687	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5186222689	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5186222690	Apr 26, 2021 (155)
24	HUGCELL_USP	ss5472065291	Oct 15, 2022 (156)
25	HUGCELL_USP	ss5472065292	Oct 15, 2022 (156)
26	HUGCELL_USP	ss5472065293	Oct 15, 2022 (156)
27	TOMMO_GENOMICS	ss5727421647	Oct 15, 2022 (156)
28	TOMMO_GENOMICS	ss5727421648	Oct 15, 2022 (156)
29	TOMMO_GENOMICS	ss5727421650	Oct 15, 2022 (156)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 280730475 (NC_000007.14:149263324::T 277/98530) Row 280730478 (NC_000007.14:149263324::TT 1791/98478) Row 280730479 (NC_000007.14:149263324::TTT 7/98548)...	-	Apr 26, 2021 (155)
40	Korean Genome Project Submission ignored due to conflicting rows: Row 19222654 (NC_000007.14:149263326::T 11/1828) Row 19222655 (NC_000007.14:149263326::TT 16/1828) Row 19222656 (NC_000007.14:149263324:TT: 9/1828)...	-	Apr 26, 2020 (154)
41	Korean Genome Project Submission ignored due to conflicting rows: Row 19222654 (NC_000007.14:149263326::T 11/1828) Row 19222655 (NC_000007.14:149263326::TT 16/1828) Row 19222656 (NC_000007.14:149263324:TT: 9/1828)...	-	Apr 26, 2020 (154)
42	Korean Genome Project Submission ignored due to conflicting rows: Row 19222654 (NC_000007.14:149263326::T 11/1828) Row 19222655 (NC_000007.14:149263326::TT 16/1828) Row 19222656 (NC_000007.14:149263324:TT: 9/1828)...	-	Apr 26, 2020 (154)
43	Korean Genome Project Submission ignored due to conflicting rows: Row 19222654 (NC_000007.14:149263326::T 11/1828) Row 19222655 (NC_000007.14:149263326::TT 16/1828) Row 19222656 (NC_000007.14:149263324:TT: 9/1828)...	-	Apr 26, 2020 (154)
44	Northern Sweden	NC_000007.13 - 148960416	Jul 13, 2019 (153)
45	8.3KJPN Submission ignored due to conflicting rows: Row 44191994 (NC_000007.13:148960415::T 242/16732) Row 44191996 (NC_000007.13:148960415::TT 43/16732) Row 44191997 (NC_000007.13:148960415:TT: 50/16732)	-	Apr 26, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 44191994 (NC_000007.13:148960415::T 242/16732) Row 44191996 (NC_000007.13:148960415::TT 43/16732) Row 44191997 (NC_000007.13:148960415:TT: 50/16732)	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 44191994 (NC_000007.13:148960415::T 242/16732) Row 44191996 (NC_000007.13:148960415::TT 43/16732) Row 44191997 (NC_000007.13:148960415:TT: 50/16732)	-	Apr 26, 2021 (155)
48	14KJPN Submission ignored due to conflicting rows: Row 61258751 (NC_000007.14:149263324::T 454/28246) Row 61258752 (NC_000007.14:149263324::TT 85/28246) Row 61258754 (NC_000007.14:149263324:TT: 72/28246)	-	Oct 15, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 61258751 (NC_000007.14:149263324::T 454/28246) Row 61258752 (NC_000007.14:149263324::TT 85/28246) Row 61258754 (NC_000007.14:149263324:TT: 72/28246)	-	Oct 15, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 61258751 (NC_000007.14:149263324::T 454/28246) Row 61258752 (NC_000007.14:149263324::TT 85/28246) Row 61258754 (NC_000007.14:149263324:TT: 72/28246)	-	Oct 15, 2022 (156)
51	TopMed	NC_000007.14 - 149263325	Apr 26, 2021 (155)
52	ALFA	NC_000007.14 - 149263325	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
ss4175571243	NC_000007.14:149263324:TTTT:	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTT	(self)
ss4175571242	NC_000007.14:149263324:TTT:	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTT	(self)
ss5186222690	NC_000007.13:148960415:TT:	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTT	(self)
ss3720968446, ss3962844655, ss4175571241, ss5727421650	NC_000007.14:149263324:TT:	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTT	(self)
ss4175571240	NC_000007.14:149263324:T:	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTT	(self)
ss3720968449, ss3962844656	NC_000007.14:149263325:T:	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTT	(self)
ss5186222687	NC_000007.13:148960415::T	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss4175571232, ss5472065292, ss5727421647	NC_000007.14:149263324::T	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3720968450, ss3962844653	NC_000007.14:149263326::T	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTT	(self)
8476681, ss3735191816, ss5186222689	NC_000007.13:148960415::TT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4175571235, ss5472065291, ss5727421648	NC_000007.14:149263324::TT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3720968451, ss3962844654	NC_000007.14:149263326::TT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4175571236	NC_000007.14:149263324::TTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4175571237, ss5472065293	NC_000007.14:149263324::TTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4175571238	NC_000007.14:149263324::TTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4175571239	NC_000007.14:149263324::TTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
605944854, ss4768567295	NC_000007.14:149263324::TTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10951660709	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:149263324:TTTTTTTTTT:… NC_000007.14:149263324:TTTTTTTTTT:TTTTTTTTTTTTTTTTT	(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 rs1210367064

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

rs1210367064