Name: rs376952972
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.

rs376952972

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:46941335-46941349 (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: delTATA / delTA / dupTA / dupTATA
Variation Type: Indel Insertion and Deletion
Frequency: dupTA=0.00085 (24/28258, 14KJPN)
dupTA=0.00095 (16/16760, 8.3KJPN)
delTATA=0.00000 (0/13610, ALFA) (+ 5 more)
delTA=0.00000 (0/13610, ALFA)
dupTA=0.00000 (0/13610, ALFA)
dupTATA=0.00000 (0/13610, ALFA)
delTATA=0.0188 (94/5008, 1000G)
delTA=0.0011 (2/1828, Korea1K)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TBC1D22A : Intron Variant
LOC105369161 : 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	13610	ATATATATATATATA=1.00000	ATATATATATA=0.00000, ATATATATATATA=0.00000, ATATATATATATATATA=0.00000, ATATATATATATATATATA=0.00000	1.0	N/A
European	Sub	9680	ATATATATATATATA=1.0000	ATATATATATA=0.0000, ATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000	1.0	N/A
African	Sub	2494	ATATATATATATATA=1.0000	ATATATATATA=0.0000, ATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000	1.0	N/A
African Others	Sub	94	ATATATATATATATA=1.00	ATATATATATA=0.00, ATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00	1.0	N/A
African American	Sub	2400	ATATATATATATATA=1.0000	ATATATATATA=0.0000, ATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000	1.0	N/A
Asian	Sub	112	ATATATATATATATA=1.000	ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000	1.0	N/A
East Asian	Sub	86	ATATATATATATATA=1.00	ATATATATATA=0.00, ATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00	1.0	N/A
Other Asian	Sub	26	ATATATATATATATA=1.00	ATATATATATA=0.00, ATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00	1.0	N/A
Latin American 1	Sub	146	ATATATATATATATA=1.000	ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000	1.0	N/A
Latin American 2	Sub	606	ATATATATATATATA=1.000	ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000	1.0	N/A
South Asian	Sub	98	ATATATATATATATA=1.00	ATATATATATA=0.00, ATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00	1.0	N/A
Other	Sub	474	ATATATATATATATA=1.000	ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=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
14KJPN	JAPANESE	Study-wide	28258	- No frequency provided	dupTA=0.00085
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	dupTA=0.00095
Allele Frequency Aggregator	Total	Global	13610	(AT)₇A=1.00000	delTATA=0.00000, delTA=0.00000, dupTA=0.00000, dupTATA=0.00000
Allele Frequency Aggregator	European	Sub	9680	(AT)₇A=1.0000	delTATA=0.0000, delTA=0.0000, dupTA=0.0000, dupTATA=0.0000
Allele Frequency Aggregator	African	Sub	2494	(AT)₇A=1.0000	delTATA=0.0000, delTA=0.0000, dupTA=0.0000, dupTATA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	606	(AT)₇A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000
Allele Frequency Aggregator	Other	Sub	474	(AT)₇A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(AT)₇A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000
Allele Frequency Aggregator	Asian	Sub	112	(AT)₇A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(AT)₇A=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00
1000Genomes	Global	Study-wide	5008	(AT)₇A=0.9798	delTATA=0.0188
1000Genomes	African	Sub	1322	(AT)₇A=0.9289	delTATA=0.0688
1000Genomes	East Asian	Sub	1008	(AT)₇A=0.9950	delTATA=0.0010
1000Genomes	Europe	Sub	1006	(AT)₇A=1.0000	delTATA=0.0000
1000Genomes	South Asian	Sub	978	(AT)₇A=1.000	delTATA=0.000
1000Genomes	American	Sub	694	(AT)₇A=0.997	delTATA=0.003
Korean Genome Project	KOREAN	Study-wide	1828	(AT)₇A=0.9989	delTA=0.0011

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 22	NC_000022.11:g.46941336TA[5]
GRCh38.p14 chr 22	NC_000022.11:g.46941336TA[6]
GRCh38.p14 chr 22	NC_000022.11:g.46941336TA[8]
GRCh38.p14 chr 22	NC_000022.11:g.46941336TA[9]
GRCh37.p13 chr 22	NC_000022.10:g.47337232TA[5]
GRCh37.p13 chr 22	NC_000022.10:g.47337232TA[6]
GRCh37.p13 chr 22	NC_000022.10:g.47337232TA[8]
GRCh37.p13 chr 22	NC_000022.10:g.47337232TA[9]

Gene: TBC1D22A, TBC1 domain family member 22A (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TBC1D22A transcript variant 2	NM_001284303.2:c.781+2914… NM_001284303.2:c.781+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant 3	NM_001284304.2:c.925+2914… NM_001284304.2:c.925+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant 4	NM_001284305.2:c.874+2914… NM_001284305.2:c.874+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant 1	NM_014346.5:c.1015+29147A… NM_014346.5:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant 5	NR_104292.1:n.	N/A	Intron Variant
TBC1D22A transcript variant X5	XM_011530100.4:c.1015+291… XM_011530100.4:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X7	XM_011530101.4:c.1015+291… XM_011530101.4:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X12	XM_011530102.4:c.1015+291… XM_011530102.4:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X2	XM_017028742.3:c.1015+291… XM_017028742.3:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X3	XM_017028743.3:c.1015+291… XM_017028743.3:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X4	XM_017028745.3:c.838+2914… XM_017028745.3:c.838+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X6	XM_017028746.3:c.1015+291… XM_017028746.3:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X1	XM_047441306.1:c.1015+291… XM_047441306.1:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X4	XM_047441307.1:c.1015+291… XM_047441307.1:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X11	XM_047441308.1:c.1015+291… XM_047441308.1:c.1015+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X13	XM_047441309.1:c.838+2914… XM_047441309.1:c.838+29147AT[5]	N/A	Intron Variant
TBC1D22A transcript variant X10	XM_017028747.3:c.	N/A	Genic Downstream Transcript Variant
TBC1D22A transcript variant X8	XR_007067970.1:n.	N/A	Genic Downstream Transcript Variant
TBC1D22A transcript variant X9	XR_007067971.1:n.	N/A	Genic Downstream Transcript Variant

Gene: LOC105369161, uncharacterized LOC105369161 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105369161 transcript variant X1	XR_938320.3: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	(AT)₇A=	delTATA	delTA	dupTA	dupTATA
GRCh38.p14 chr 22	NC_000022.11:g.46941335_46941349=	NC_000022.11:g.46941336TA[5]	NC_000022.11:g.46941336TA[6]	NC_000022.11:g.46941336TA[8]	NC_000022.11:g.46941336TA[9]
GRCh37.p13 chr 22	NC_000022.10:g.47337231_47337245=	NC_000022.10:g.47337232TA[5]	NC_000022.10:g.47337232TA[6]	NC_000022.10:g.47337232TA[8]	NC_000022.10:g.47337232TA[9]
TBC1D22A transcript variant 2	NM_001284303.2:c.781+29147=	NM_001284303.2:c.781+29147AT[5]	NM_001284303.2:c.781+29147AT[6]	NM_001284303.2:c.781+29147AT[8]	NM_001284303.2:c.781+29147AT[9]
TBC1D22A transcript variant 3	NM_001284304.2:c.925+29147=	NM_001284304.2:c.925+29147AT[5]	NM_001284304.2:c.925+29147AT[6]	NM_001284304.2:c.925+29147AT[8]	NM_001284304.2:c.925+29147AT[9]
TBC1D22A transcript variant 4	NM_001284305.2:c.874+29147=	NM_001284305.2:c.874+29147AT[5]	NM_001284305.2:c.874+29147AT[6]	NM_001284305.2:c.874+29147AT[8]	NM_001284305.2:c.874+29147AT[9]
TBC1D22A transcript	NM_014346.2:c.1015+29147=	NM_014346.2:c.1015+29147AT[5]	NM_014346.2:c.1015+29147AT[6]	NM_014346.2:c.1015+29147AT[8]	NM_014346.2:c.1015+29147AT[9]
TBC1D22A transcript variant 1	NM_014346.5:c.1015+29147=	NM_014346.5:c.1015+29147AT[5]	NM_014346.5:c.1015+29147AT[6]	NM_014346.5:c.1015+29147AT[8]	NM_014346.5:c.1015+29147AT[9]
TBC1D22A transcript variant X1	XM_005261492.1:c.925+29147=	XM_005261492.1:c.925+29147AT[5]	XM_005261492.1:c.925+29147AT[6]	XM_005261492.1:c.925+29147AT[8]	XM_005261492.1:c.925+29147AT[9]
TBC1D22A transcript variant X2	XM_005261493.1:c.874+29147=	XM_005261493.1:c.874+29147AT[5]	XM_005261493.1:c.874+29147AT[6]	XM_005261493.1:c.874+29147AT[8]	XM_005261493.1:c.874+29147AT[9]
TBC1D22A transcript variant X3	XM_005261494.1:c.781+29147=	XM_005261494.1:c.781+29147AT[5]	XM_005261494.1:c.781+29147AT[6]	XM_005261494.1:c.781+29147AT[8]	XM_005261494.1:c.781+29147AT[9]
TBC1D22A transcript variant X4	XM_005261495.1:c.673+29147=	XM_005261495.1:c.673+29147AT[5]	XM_005261495.1:c.673+29147AT[6]	XM_005261495.1:c.673+29147AT[8]	XM_005261495.1:c.673+29147AT[9]
TBC1D22A transcript variant X5	XM_011530100.4:c.1015+29147=	XM_011530100.4:c.1015+29147AT[5]	XM_011530100.4:c.1015+29147AT[6]	XM_011530100.4:c.1015+29147AT[8]	XM_011530100.4:c.1015+29147AT[9]
TBC1D22A transcript variant X7	XM_011530101.4:c.1015+29147=	XM_011530101.4:c.1015+29147AT[5]	XM_011530101.4:c.1015+29147AT[6]	XM_011530101.4:c.1015+29147AT[8]	XM_011530101.4:c.1015+29147AT[9]
TBC1D22A transcript variant X12	XM_011530102.4:c.1015+29147=	XM_011530102.4:c.1015+29147AT[5]	XM_011530102.4:c.1015+29147AT[6]	XM_011530102.4:c.1015+29147AT[8]	XM_011530102.4:c.1015+29147AT[9]
TBC1D22A transcript variant X2	XM_017028742.3:c.1015+29147=	XM_017028742.3:c.1015+29147AT[5]	XM_017028742.3:c.1015+29147AT[6]	XM_017028742.3:c.1015+29147AT[8]	XM_017028742.3:c.1015+29147AT[9]
TBC1D22A transcript variant X3	XM_017028743.3:c.1015+29147=	XM_017028743.3:c.1015+29147AT[5]	XM_017028743.3:c.1015+29147AT[6]	XM_017028743.3:c.1015+29147AT[8]	XM_017028743.3:c.1015+29147AT[9]
TBC1D22A transcript variant X4	XM_017028745.3:c.838+29147=	XM_017028745.3:c.838+29147AT[5]	XM_017028745.3:c.838+29147AT[6]	XM_017028745.3:c.838+29147AT[8]	XM_017028745.3:c.838+29147AT[9]
TBC1D22A transcript variant X6	XM_017028746.3:c.1015+29147=	XM_017028746.3:c.1015+29147AT[5]	XM_017028746.3:c.1015+29147AT[6]	XM_017028746.3:c.1015+29147AT[8]	XM_017028746.3:c.1015+29147AT[9]
TBC1D22A transcript variant X1	XM_047441306.1:c.1015+29147=	XM_047441306.1:c.1015+29147AT[5]	XM_047441306.1:c.1015+29147AT[6]	XM_047441306.1:c.1015+29147AT[8]	XM_047441306.1:c.1015+29147AT[9]
TBC1D22A transcript variant X4	XM_047441307.1:c.1015+29147=	XM_047441307.1:c.1015+29147AT[5]	XM_047441307.1:c.1015+29147AT[6]	XM_047441307.1:c.1015+29147AT[8]	XM_047441307.1:c.1015+29147AT[9]
TBC1D22A transcript variant X11	XM_047441308.1:c.1015+29147=	XM_047441308.1:c.1015+29147AT[5]	XM_047441308.1:c.1015+29147AT[6]	XM_047441308.1:c.1015+29147AT[8]	XM_047441308.1:c.1015+29147AT[9]
TBC1D22A transcript variant X13	XM_047441309.1:c.838+29147=	XM_047441309.1:c.838+29147AT[5]	XM_047441309.1:c.838+29147AT[6]	XM_047441309.1:c.838+29147AT[8]	XM_047441309.1:c.838+29147AT[9]

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#.

18 SubSNP, 9 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	LUNTER	ss553154765	Apr 25, 2013 (138)
2	1000GENOMES	ss1379129189	Aug 21, 2014 (142)
3	EVA_DECODE	ss3708370328	Jul 13, 2019 (153)
4	EVA_DECODE	ss3708370329	Jul 13, 2019 (153)
5	EVA_DECODE	ss3708370330	Jul 13, 2019 (153)
6	KHV_HUMAN_GENOMES	ss3822644390	Jul 13, 2019 (153)
7	KOGIC	ss3983822648	Apr 27, 2020 (154)
8	GNOMAD	ss4366024270	Apr 27, 2021 (155)
9	GNOMAD	ss4366024271	Apr 27, 2021 (155)
10	GNOMAD	ss4366024275	Apr 27, 2021 (155)
11	GNOMAD	ss4366024276	Apr 27, 2021 (155)
12	TOMMO_GENOMICS	ss5233029670	Apr 27, 2021 (155)
13	1000G_HIGH_COVERAGE	ss5311402430	Oct 16, 2022 (156)
14	1000G_HIGH_COVERAGE	ss5311402431	Oct 16, 2022 (156)
15	HUGCELL_USP	ss5503214957	Oct 16, 2022 (156)
16	HUGCELL_USP	ss5503214958	Oct 16, 2022 (156)
17	SANFORD_IMAGENETICS	ss5664659628	Oct 16, 2022 (156)
18	TOMMO_GENOMICS	ss5794283219	Oct 16, 2022 (156)
19	1000Genomes	NC_000022.10 - 47337231	Oct 12, 2018 (152)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 572404588 (NC_000022.11:46941334::AT 122/131256) Row 572404589 (NC_000022.11:46941334::ATAT 0/131268) Row 572404593 (NC_000022.11:46941334:AT: 13/131252)...	-	Apr 27, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 572404588 (NC_000022.11:46941334::AT 122/131256) Row 572404589 (NC_000022.11:46941334::ATAT 0/131268) Row 572404593 (NC_000022.11:46941334:AT: 13/131252)...	-	Apr 27, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 572404588 (NC_000022.11:46941334::AT 122/131256) Row 572404589 (NC_000022.11:46941334::ATAT 0/131268) Row 572404593 (NC_000022.11:46941334:AT: 13/131252)...	-	Apr 27, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 572404588 (NC_000022.11:46941334::AT 122/131256) Row 572404589 (NC_000022.11:46941334::ATAT 0/131268) Row 572404593 (NC_000022.11:46941334:AT: 13/131252)...	-	Apr 27, 2021 (155)
24	Korean Genome Project	NC_000022.11 - 46941335	Apr 27, 2020 (154)
25	8.3KJPN	NC_000022.10 - 47337231	Apr 27, 2021 (155)
26	14KJPN	NC_000022.11 - 46941335	Oct 16, 2022 (156)
27	ALFA	NC_000022.11 - 46941335	Apr 27, 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
ss553154765	NC_000022.9:45715894:ATAT:	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATA	(self)
81063592, ss1379129189, ss5664659628	NC_000022.10:47337230:ATAT:	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATA	(self)
ss3708370330, ss3822644390, ss4366024276, ss5311402430, ss5503214957	NC_000022.11:46941334:ATAT:	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATA	(self)
1284929811	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATA	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATA	(self)
40200649, ss3983822648, ss4366024275	NC_000022.11:46941334:AT:	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATA	(self)
1284929811	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATA	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATA	(self)
ss3708370329	NC_000022.11:46941336:AT:	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATA	(self)
90998977, ss5233029670	NC_000022.10:47337230::AT	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATA	(self)
128120323, ss4366024270, ss5311402431, ss5503214958, ss5794283219	NC_000022.11:46941334::AT	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATA	(self)
1284929811	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATA	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATA	(self)
ss3708370328	NC_000022.11:46941338::AT	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATA	(self)
ss4366024271	NC_000022.11:46941334::ATAT	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATATA	(self)
1284929811	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATATA	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATATATATA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2415024247	NC_000022.10:47337230:AT:	NC_000022.11:46941334:ATATATATATAT… NC_000022.11:46941334:ATATATATATATATA:ATATATATATATA

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

No publications for rs376952972

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs376952972