Name: rs371373270
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.

rs371373270

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:115144038-115144047 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.2349 (1808/7698, ALFA)
(T)₁₀=0.4397 (2202/5008, 1000G)
dupTT=0.4059 (1815/4472, Estonian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRIM36 : 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	7698	TTTTTTTTTT=0.7646	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0005, TTTTTTTTTTTT=0.2349, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	0.627308	0.096749	0.275943	32
European	Sub	7124	TTTTTTTTTT=0.7462	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0006, TTTTTTTTTTTT=0.2532, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	0.59837	0.104553	0.297077	32
African	Sub	264	TTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	10	TTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	254	TTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	14	TTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	10	TTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	38	TTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	110	TTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	TTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	110	TTTTTTTTTT=0.964	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.036, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	0.927273	0.0	0.072727	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7698	(T)₁₀=0.7646	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0005, dupTT=0.2349, dupTTT=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	European	Sub	7124	(T)₁₀=0.7462	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0006, dupTT=0.2532, dupTTT=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	African	Sub	264	(T)₁₀=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	110	(T)₁₀=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	110	(T)₁₀=0.964	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.036, dupTTT=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	38	(T)₁₀=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	38	(T)₁₀=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	14	(T)₁₀=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₆=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.0523, dupTT=0.5080
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.1884, dupTT=0.5106
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.0000, dupTT=0.7242
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.0000, dupTT=0.3857
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.004, dupTT=0.391
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.013, dupTT=0.532
Genetic variation in the Estonian population	Estonian	Study-wide	4472	- No frequency provided	dupTT=0.4059

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 5	NC_000005.10:g.115144045_115144047del
GRCh38.p14 chr 5	NC_000005.10:g.115144046_115144047del
GRCh38.p14 chr 5	NC_000005.10:g.115144047del
GRCh38.p14 chr 5	NC_000005.10:g.115144047dup
GRCh38.p14 chr 5	NC_000005.10:g.115144046_115144047dup
GRCh38.p14 chr 5	NC_000005.10:g.115144045_115144047dup
GRCh38.p14 chr 5	NC_000005.10:g.115144042_115144047dup
GRCh37.p13 chr 5	NC_000005.9:g.114479742_114479744del
GRCh37.p13 chr 5	NC_000005.9:g.114479743_114479744del
GRCh37.p13 chr 5	NC_000005.9:g.114479744del
GRCh37.p13 chr 5	NC_000005.9:g.114479744dup
GRCh37.p13 chr 5	NC_000005.9:g.114479743_114479744dup
GRCh37.p13 chr 5	NC_000005.9:g.114479742_114479744dup
GRCh37.p13 chr 5	NC_000005.9:g.114479739_114479744dup

Gene: TRIM36, tripartite motif containing 36 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TRIM36 transcript variant 4	NM_001300752.2:c.306+558_… NM_001300752.2:c.306+558_306+560del	N/A	Intron Variant
TRIM36 transcript variant 5	NM_001300759.2:c.735+558_… NM_001300759.2:c.735+558_735+560del	N/A	Intron Variant
TRIM36 transcript variant 1	NM_018700.4:c.771+558_771… NM_018700.4:c.771+558_771+560del	N/A	Intron Variant
TRIM36 transcript variant 2	NM_001017397.2:c.	N/A	Genic Downstream Transcript Variant
TRIM36 transcript variant 3	NM_001017398.2:c.	N/A	Genic Downstream Transcript Variant
TRIM36 transcript variant X1	XM_017009621.3:c.822+558_… XM_017009621.3:c.822+558_822+560del	N/A	Intron Variant
TRIM36 transcript variant X2	XM_017009622.3:c.786+558_… XM_017009622.3:c.786+558_786+560del	N/A	Intron Variant
TRIM36 transcript variant X5	XM_017009623.3:c.822+558_… XM_017009623.3:c.822+558_822+560del	N/A	Intron Variant
TRIM36 transcript variant X3	XM_047417360.1:c.504+558_… XM_047417360.1:c.504+558_504+560del	N/A	Intron Variant
TRIM36 transcript variant X4	XM_047417361.1:c.306+558_… XM_047417361.1:c.306+558_306+560del	N/A	Intron Variant
TRIM36 transcript variant X6	XM_047417362.1:c.822+558_… XM_047417362.1:c.822+558_822+560del	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)₁₀=	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₆
GRCh38.p14 chr 5	NC_000005.10:g.115144038_115144047=	NC_000005.10:g.115144045_115144047del	NC_000005.10:g.115144046_115144047del	NC_000005.10:g.115144047del	NC_000005.10:g.115144047dup	NC_000005.10:g.115144046_115144047dup	NC_000005.10:g.115144045_115144047dup	NC_000005.10:g.115144042_115144047dup
GRCh37.p13 chr 5	NC_000005.9:g.114479735_114479744=	NC_000005.9:g.114479742_114479744del	NC_000005.9:g.114479743_114479744del	NC_000005.9:g.114479744del	NC_000005.9:g.114479744dup	NC_000005.9:g.114479743_114479744dup	NC_000005.9:g.114479742_114479744dup	NC_000005.9:g.114479739_114479744dup
TRIM36 transcript variant 4	NM_001300752.2:c.306+560=	NM_001300752.2:c.306+558_306+560del	NM_001300752.2:c.306+559_306+560del	NM_001300752.2:c.306+560del	NM_001300752.2:c.306+560dup	NM_001300752.2:c.306+559_306+560dup	NM_001300752.2:c.306+558_306+560dup	NM_001300752.2:c.306+555_306+560dup
TRIM36 transcript variant 5	NM_001300759.2:c.735+560=	NM_001300759.2:c.735+558_735+560del	NM_001300759.2:c.735+559_735+560del	NM_001300759.2:c.735+560del	NM_001300759.2:c.735+560dup	NM_001300759.2:c.735+559_735+560dup	NM_001300759.2:c.735+558_735+560dup	NM_001300759.2:c.735+555_735+560dup
TRIM36 transcript variant 1	NM_018700.3:c.771+560=	NM_018700.3:c.771+558_771+560del	NM_018700.3:c.771+559_771+560del	NM_018700.3:c.771+560del	NM_018700.3:c.771+560dup	NM_018700.3:c.771+559_771+560dup	NM_018700.3:c.771+558_771+560dup	NM_018700.3:c.771+555_771+560dup
TRIM36 transcript variant 1	NM_018700.4:c.771+560=	NM_018700.4:c.771+558_771+560del	NM_018700.4:c.771+559_771+560del	NM_018700.4:c.771+560del	NM_018700.4:c.771+560dup	NM_018700.4:c.771+559_771+560dup	NM_018700.4:c.771+558_771+560dup	NM_018700.4:c.771+555_771+560dup
TRIM36 transcript variant X1	XM_005272031.1:c.735+560=	XM_005272031.1:c.735+558_735+560del	XM_005272031.1:c.735+559_735+560del	XM_005272031.1:c.735+560del	XM_005272031.1:c.735+560dup	XM_005272031.1:c.735+559_735+560dup	XM_005272031.1:c.735+558_735+560dup	XM_005272031.1:c.735+555_735+560dup
TRIM36 transcript variant X2	XM_005272032.1:c.477+560=	XM_005272032.1:c.477+558_477+560del	XM_005272032.1:c.477+559_477+560del	XM_005272032.1:c.477+560del	XM_005272032.1:c.477+560dup	XM_005272032.1:c.477+559_477+560dup	XM_005272032.1:c.477+558_477+560dup	XM_005272032.1:c.477+555_477+560dup
TRIM36 transcript variant X3	XM_005272033.1:c.306+560=	XM_005272033.1:c.306+558_306+560del	XM_005272033.1:c.306+559_306+560del	XM_005272033.1:c.306+560del	XM_005272033.1:c.306+560dup	XM_005272033.1:c.306+559_306+560dup	XM_005272033.1:c.306+558_306+560dup	XM_005272033.1:c.306+555_306+560dup
TRIM36 transcript variant X4	XM_005272034.1:c.771+560=	XM_005272034.1:c.771+558_771+560del	XM_005272034.1:c.771+559_771+560del	XM_005272034.1:c.771+560del	XM_005272034.1:c.771+560dup	XM_005272034.1:c.771+559_771+560dup	XM_005272034.1:c.771+558_771+560dup	XM_005272034.1:c.771+555_771+560dup
TRIM36 transcript variant X1	XM_017009621.3:c.822+560=	XM_017009621.3:c.822+558_822+560del	XM_017009621.3:c.822+559_822+560del	XM_017009621.3:c.822+560del	XM_017009621.3:c.822+560dup	XM_017009621.3:c.822+559_822+560dup	XM_017009621.3:c.822+558_822+560dup	XM_017009621.3:c.822+555_822+560dup
TRIM36 transcript variant X2	XM_017009622.3:c.786+560=	XM_017009622.3:c.786+558_786+560del	XM_017009622.3:c.786+559_786+560del	XM_017009622.3:c.786+560del	XM_017009622.3:c.786+560dup	XM_017009622.3:c.786+559_786+560dup	XM_017009622.3:c.786+558_786+560dup	XM_017009622.3:c.786+555_786+560dup
TRIM36 transcript variant X5	XM_017009623.3:c.822+560=	XM_017009623.3:c.822+558_822+560del	XM_017009623.3:c.822+559_822+560del	XM_017009623.3:c.822+560del	XM_017009623.3:c.822+560dup	XM_017009623.3:c.822+559_822+560dup	XM_017009623.3:c.822+558_822+560dup	XM_017009623.3:c.822+555_822+560dup
TRIM36 transcript variant X3	XM_047417360.1:c.504+560=	XM_047417360.1:c.504+558_504+560del	XM_047417360.1:c.504+559_504+560del	XM_047417360.1:c.504+560del	XM_047417360.1:c.504+560dup	XM_047417360.1:c.504+559_504+560dup	XM_047417360.1:c.504+558_504+560dup	XM_047417360.1:c.504+555_504+560dup
TRIM36 transcript variant X4	XM_047417361.1:c.306+560=	XM_047417361.1:c.306+558_306+560del	XM_047417361.1:c.306+559_306+560del	XM_047417361.1:c.306+560del	XM_047417361.1:c.306+560dup	XM_047417361.1:c.306+559_306+560dup	XM_047417361.1:c.306+558_306+560dup	XM_047417361.1:c.306+555_306+560dup
TRIM36 transcript variant X6	XM_047417362.1:c.822+560=	XM_047417362.1:c.822+558_822+560del	XM_047417362.1:c.822+559_822+560del	XM_047417362.1:c.822+560del	XM_047417362.1:c.822+560dup	XM_047417362.1:c.822+559_822+560dup	XM_047417362.1:c.822+558_822+560dup	XM_047417362.1:c.822+555_822+560dup

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#.

50 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	LUNTER	ss551534058	Apr 25, 2013 (138)
2	LUNTER	ss551699733	Apr 25, 2013 (138)
3	LUNTER	ss553212985	Apr 25, 2013 (138)
4	SSMP	ss663551218	Apr 01, 2015 (144)
5	1000GENOMES	ss1374339651	Aug 21, 2014 (142)
6	1000GENOMES	ss1374339654	Aug 21, 2014 (142)
7	DDI	ss1536475994	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1704827216	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1704827218	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1704827223	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1704827225	Apr 01, 2015 (144)
12	JJLAB	ss2030707889	Sep 14, 2016 (149)
13	SYSTEMSBIOZJU	ss2626106392	Nov 08, 2017 (151)
14	SWEGEN	ss2997597816	Nov 08, 2017 (151)
15	SWEGEN	ss2997597817	Nov 08, 2017 (151)
16	MCHAISSO	ss3065047056	Nov 08, 2017 (151)
17	MCHAISSO	ss3066037065	Nov 08, 2017 (151)
18	BIOINF_KMB_FNS_UNIBA	ss3645901103	Oct 12, 2018 (152)
19	EGCUT_WGS	ss3665500010	Jul 13, 2019 (153)
20	EVA_DECODE	ss3715467152	Jul 13, 2019 (153)
21	EVA_DECODE	ss3715467153	Jul 13, 2019 (153)
22	ACPOP	ss3732711306	Jul 13, 2019 (153)
23	ACPOP	ss3732711307	Jul 13, 2019 (153)
24	PACBIO	ss3785217863	Jul 13, 2019 (153)
25	PACBIO	ss3790606628	Jul 13, 2019 (153)
26	PACBIO	ss3795483404	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3807085289	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3807085290	Jul 13, 2019 (153)
29	EVA	ss3829444281	Apr 26, 2020 (154)
30	KOGIC	ss3957430738	Apr 26, 2020 (154)
31	KOGIC	ss3957430739	Apr 26, 2020 (154)
32	GNOMAD	ss4127207504	Apr 26, 2021 (155)
33	GNOMAD	ss4127207505	Apr 26, 2021 (155)
34	GNOMAD	ss4127207506	Apr 26, 2021 (155)
35	GNOMAD	ss4127207507	Apr 26, 2021 (155)
36	GNOMAD	ss4127207508	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5173599124	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5173599125	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5265411895	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5265411896	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5265411897	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5463425848	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5463425849	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5463425850	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5710521471	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5710521473	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5710521474	Oct 13, 2022 (156)
48	YY_MCH	ss5806664852	Oct 13, 2022 (156)
49	EVA	ss5835477818	Oct 13, 2022 (156)
50	EVA	ss5854970615	Oct 13, 2022 (156)
51	1000Genomes	NC_000005.9 - 114479735	Oct 12, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 15785929 (NC_000005.9:114479734::TT 1544/3854) Row 15785930 (NC_000005.9:114479734::TTT 17/3854)	-	Oct 12, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 15785929 (NC_000005.9:114479734::TT 1544/3854) Row 15785930 (NC_000005.9:114479734::TTT 17/3854)	-	Oct 12, 2018 (152)
54	Genetic variation in the Estonian population	NC_000005.9 - 114479735	Oct 12, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 200805313 (NC_000005.10:115144037::T 7319/137808) Row 200805314 (NC_000005.10:115144037::TT 62474/137706) Row 200805315 (NC_000005.10:115144037::TTT 699/137902)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 200805313 (NC_000005.10:115144037::T 7319/137808) Row 200805314 (NC_000005.10:115144037::TT 62474/137706) Row 200805315 (NC_000005.10:115144037::TTT 699/137902)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 200805313 (NC_000005.10:115144037::T 7319/137808) Row 200805314 (NC_000005.10:115144037::TT 62474/137706) Row 200805315 (NC_000005.10:115144037::TTT 699/137902)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 200805313 (NC_000005.10:115144037::T 7319/137808) Row 200805314 (NC_000005.10:115144037::TT 62474/137706) Row 200805315 (NC_000005.10:115144037::TTT 699/137902)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 200805313 (NC_000005.10:115144037::T 7319/137808) Row 200805314 (NC_000005.10:115144037::TT 62474/137706) Row 200805315 (NC_000005.10:115144037::TTT 699/137902)...	-	Apr 26, 2021 (155)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 13808739 (NC_000005.10:115144037::TT 1208/1832) Row 13808740 (NC_000005.10:115144037::TTT 13/1832)	-	Apr 26, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 13808739 (NC_000005.10:115144037::TT 1208/1832) Row 13808740 (NC_000005.10:115144037::TTT 13/1832)	-	Apr 26, 2020 (154)
62	Northern Sweden Submission ignored due to conflicting rows: Row 5996171 (NC_000005.9:114479734::TT 280/600) Row 5996172 (NC_000005.9:114479734::T 1/600)	-	Jul 13, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 5996171 (NC_000005.9:114479734::TT 280/600) Row 5996172 (NC_000005.9:114479734::T 1/600)	-	Jul 13, 2019 (153)
64	8.3KJPN Submission ignored due to conflicting rows: Row 31568431 (NC_000005.9:114479734::TT 11496/16760) Row 31568432 (NC_000005.9:114479734::TTT 14/16760)	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 31568431 (NC_000005.9:114479734::TT 11496/16760) Row 31568432 (NC_000005.9:114479734::TTT 14/16760)	-	Apr 26, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 44358575 (NC_000005.10:115144037::TT 19402/28258) Row 44358577 (NC_000005.10:115144037::TTT 23/28258) Row 44358578 (NC_000005.10:115144037::T 12/28258)	-	Oct 13, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 44358575 (NC_000005.10:115144037::TT 19402/28258) Row 44358577 (NC_000005.10:115144037::TTT 23/28258) Row 44358578 (NC_000005.10:115144037::T 12/28258)	-	Oct 13, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 44358575 (NC_000005.10:115144037::TT 19402/28258) Row 44358577 (NC_000005.10:115144037::TTT 23/28258) Row 44358578 (NC_000005.10:115144037::T 12/28258)	-	Oct 13, 2022 (156)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 15785929 (NC_000005.9:114479734::TT 1519/3708) Row 15785930 (NC_000005.9:114479734::TTT 12/3708)	-	Oct 12, 2018 (152)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 15785929 (NC_000005.9:114479734::TT 1519/3708) Row 15785930 (NC_000005.9:114479734::TTT 12/3708)	-	Oct 12, 2018 (152)
71	ALFA	NC_000005.10 - 115144038	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)
rs375796677	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4127207508	NC_000005.10:115144037:TTT:	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTT	(self)
8280565372	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTT	(self)
8280565372	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTT	(self)
ss4127207507	NC_000005.10:115144037:T:	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTT	(self)
8280565372	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTT	(self)
ss551699733	NC_000005.8:114507633::T	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTT	(self)
28386968, ss1374339651, ss2997597817, ss3732711307	NC_000005.9:114479734::T	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3715467152, ss3807085290, ss4127207504, ss5265411896, ss5463425849, ss5710521474	NC_000005.10:115144037::T	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTT	(self)
8280565372	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss551534058, ss553212985	NC_000005.8:114507633::TT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTT	(self)
28386968, 11238258, ss663551218, ss1374339654, ss1536475994, ss1704827216, ss1704827223, ss2030707889, ss2626106392, ss2997597816, ss3665500010, ss3732711306, ss3785217863, ss3790606628, ss3795483404, ss3829444281, ss5173599124, ss5835477818	NC_000005.9:114479734::TT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3065047056, ss3066037065, ss3645901103, ss3715467153, ss3807085289, ss3957430738, ss4127207505, ss5265411895, ss5463425848, ss5710521471, ss5806664852, ss5854970615	NC_000005.10:115144037::TT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTT	(self)
8280565372	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1704827218, ss1704827225, ss5173599125	NC_000005.9:114479734::TTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3957430739, ss4127207506, ss5265411897, ss5463425850, ss5710521473	NC_000005.10:115144037::TTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
8280565372	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
8280565372	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3475449270	NC_000005.10:115144037:TT:	NC_000005.10:115144037:TTTTTTTTTT:… NC_000005.10:115144037:TTTTTTTTTT:TTTTTTTT

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

No publications for rs371373270

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

rs371373270