Name: rs371166684
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.

rs371166684

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:112075069-112075084 (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)₆ / del(T)₄ / delTTT / delTT…
del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₅ / dup(T)₁₅ / dup(T)₁₆ / ins(T)₂₅C(T)₂₀
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₆=0.0000 (0/8224, ALFA)
delTT=0.0000 (0/8224, ALFA)
delT=0.0000 (0/8224, ALFA) (+ 4 more)
dupT=0.0000 (0/8224, ALFA)
dupTT=0.0000 (0/8224, ALFA)
(T)₁₆=0.3305 (1655/5008, 1000G)
delT=0.102 (52/510, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TUBE1 : 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	HWEP
Total	Global	8224	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	5592	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	1760	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	78	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	1682	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	44	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	40	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0	1.0	N/A
Latin American 1	Sub	96	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	384	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	26	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	322	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	8224	(T)₁₆=1.0000	del(T)₆=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	5592	(T)₁₆=1.0000	del(T)₆=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1760	(T)₁₆=1.0000	del(T)₆=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	384	(T)₁₆=1.000	del(T)₆=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	322	(T)₁₆=1.000	del(T)₆=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	96	(T)₁₆=1.00	del(T)₆=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	44	(T)₁₆=1.00	del(T)₆=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(T)₁₆=1.00	del(T)₆=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₆=0.3305	delT=0.6695
1000Genomes	African	Sub	1322	(T)₁₆=0.3631	delT=0.6369
1000Genomes	East Asian	Sub	1008	(T)₁₆=0.1687	delT=0.8313
1000Genomes	Europe	Sub	1006	(T)₁₆=0.4225	delT=0.5775
1000Genomes	South Asian	Sub	978	(T)₁₆=0.310	delT=0.690
1000Genomes	American	Sub	694	(T)₁₆=0.399	delT=0.601
Northern Sweden	ACPOP	Study-wide	510	(T)₁₆=0.898	delT=0.102

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 6	NC_000006.12:g.112075079_112075084del
GRCh38.p14 chr 6	NC_000006.12:g.112075081_112075084del
GRCh38.p14 chr 6	NC_000006.12:g.112075082_112075084del
GRCh38.p14 chr 6	NC_000006.12:g.112075083_112075084del
GRCh38.p14 chr 6	NC_000006.12:g.112075084del
GRCh38.p14 chr 6	NC_000006.12:g.112075084dup
GRCh38.p14 chr 6	NC_000006.12:g.112075083_112075084dup
GRCh38.p14 chr 6	NC_000006.12:g.112075082_112075084dup
GRCh38.p14 chr 6	NC_000006.12:g.112075080_112075084dup
GRCh38.p14 chr 6	NC_000006.12:g.112075070_112075084dup
GRCh38.p14 chr 6	NC_000006.12:g.112075069_112075084dup
GRCh38.p14 chr 6	NC_000006.12:g.112075069_112075084T[41]CTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72601_72606del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72603_72606del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72604_72606del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72605_72606del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72606del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72606dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72605_72606dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72604_72606dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72602_72606dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72592_72606dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72591_72606dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72591_72606T[41]CTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 6	NC_000006.11:g.112396282_112396287del
GRCh37.p13 chr 6	NC_000006.11:g.112396284_112396287del
GRCh37.p13 chr 6	NC_000006.11:g.112396285_112396287del
GRCh37.p13 chr 6	NC_000006.11:g.112396286_112396287del
GRCh37.p13 chr 6	NC_000006.11:g.112396287del
GRCh37.p13 chr 6	NC_000006.11:g.112396287dup
GRCh37.p13 chr 6	NC_000006.11:g.112396286_112396287dup
GRCh37.p13 chr 6	NC_000006.11:g.112396285_112396287dup
GRCh37.p13 chr 6	NC_000006.11:g.112396283_112396287dup
GRCh37.p13 chr 6	NC_000006.11:g.112396273_112396287dup
GRCh37.p13 chr 6	NC_000006.11:g.112396272_112396287dup
GRCh37.p13 chr 6	NC_000006.11:g.112396272_112396287T[41]CTTTTTTTTTTTTTTTTTTTT[1]

Gene: TUBE1, tubulin epsilon 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TUBE1 transcript	NM_016262.5:c.813-224_813… NM_016262.5:c.813-224_813-219del	N/A	Intron Variant
TUBE1 transcript variant X1	XM_047418854.1:c.681-224_… XM_047418854.1:c.681-224_681-219del	N/A	Intron Variant
TUBE1 transcript variant X2	XM_047418855.1:c.588-224_… XM_047418855.1:c.588-224_588-219del	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)₁₆=	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₅	dup(T)₁₅	dup(T)₁₆	ins(T)₂₅C(T)₂₀
GRCh38.p14 chr 6	NC_000006.12:g.112075069_112075084=	NC_000006.12:g.112075079_112075084del	NC_000006.12:g.112075081_112075084del	NC_000006.12:g.112075082_112075084del	NC_000006.12:g.112075083_112075084del	NC_000006.12:g.112075084del	NC_000006.12:g.112075084dup	NC_000006.12:g.112075083_112075084dup	NC_000006.12:g.112075082_112075084dup	NC_000006.12:g.112075080_112075084dup	NC_000006.12:g.112075070_112075084dup	NC_000006.12:g.112075069_112075084dup	NC_000006.12:g.112075069_112075084T[41]CTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.72591_72606=	NW_003871062.1:g.72601_72606del	NW_003871062.1:g.72603_72606del	NW_003871062.1:g.72604_72606del	NW_003871062.1:g.72605_72606del	NW_003871062.1:g.72606del	NW_003871062.1:g.72606dup	NW_003871062.1:g.72605_72606dup	NW_003871062.1:g.72604_72606dup	NW_003871062.1:g.72602_72606dup	NW_003871062.1:g.72592_72606dup	NW_003871062.1:g.72591_72606dup	NW_003871062.1:g.72591_72606T[41]CTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 6	NC_000006.11:g.112396272_112396287=	NC_000006.11:g.112396282_112396287del	NC_000006.11:g.112396284_112396287del	NC_000006.11:g.112396285_112396287del	NC_000006.11:g.112396286_112396287del	NC_000006.11:g.112396287del	NC_000006.11:g.112396287dup	NC_000006.11:g.112396286_112396287dup	NC_000006.11:g.112396285_112396287dup	NC_000006.11:g.112396283_112396287dup	NC_000006.11:g.112396273_112396287dup	NC_000006.11:g.112396272_112396287dup	NC_000006.11:g.112396272_112396287T[41]CTTTTTTTTTTTTTTTTTTTT[1]
TUBE1 transcript	NM_016262.4:c.813-219=	NM_016262.4:c.813-224_813-219del	NM_016262.4:c.813-222_813-219del	NM_016262.4:c.813-221_813-219del	NM_016262.4:c.813-220_813-219del	NM_016262.4:c.813-219del	NM_016262.4:c.813-219dup	NM_016262.4:c.813-220_813-219dup	NM_016262.4:c.813-221_813-219dup	NM_016262.4:c.813-223_813-219dup	NM_016262.4:c.813-233_813-219dup	NM_016262.4:c.813-234_813-219dup	NM_016262.4:c.813-219_813-218insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA
TUBE1 transcript	NM_016262.5:c.813-219=	NM_016262.5:c.813-224_813-219del	NM_016262.5:c.813-222_813-219del	NM_016262.5:c.813-221_813-219del	NM_016262.5:c.813-220_813-219del	NM_016262.5:c.813-219del	NM_016262.5:c.813-219dup	NM_016262.5:c.813-220_813-219dup	NM_016262.5:c.813-221_813-219dup	NM_016262.5:c.813-223_813-219dup	NM_016262.5:c.813-233_813-219dup	NM_016262.5:c.813-234_813-219dup	NM_016262.5:c.813-219_813-218insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA
TUBE1 transcript variant X1	XM_005267007.1:c.588-219=	XM_005267007.1:c.588-224_588-219del	XM_005267007.1:c.588-222_588-219del	XM_005267007.1:c.588-221_588-219del	XM_005267007.1:c.588-220_588-219del	XM_005267007.1:c.588-219del	XM_005267007.1:c.588-219dup	XM_005267007.1:c.588-220_588-219dup	XM_005267007.1:c.588-221_588-219dup	XM_005267007.1:c.588-223_588-219dup	XM_005267007.1:c.588-233_588-219dup	XM_005267007.1:c.588-234_588-219dup	XM_005267007.1:c.588-219_588-218insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA
TUBE1 transcript variant X1	XM_005277551.1:c.588-219=	XM_005277551.1:c.588-224_588-219del	XM_005277551.1:c.588-222_588-219del	XM_005277551.1:c.588-221_588-219del	XM_005277551.1:c.588-220_588-219del	XM_005277551.1:c.588-219del	XM_005277551.1:c.588-219dup	XM_005277551.1:c.588-220_588-219dup	XM_005277551.1:c.588-221_588-219dup	XM_005277551.1:c.588-223_588-219dup	XM_005277551.1:c.588-233_588-219dup	XM_005277551.1:c.588-234_588-219dup	XM_005277551.1:c.588-219_588-218insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA
TUBE1 transcript variant X1	XM_047418854.1:c.681-219=	XM_047418854.1:c.681-224_681-219del	XM_047418854.1:c.681-222_681-219del	XM_047418854.1:c.681-221_681-219del	XM_047418854.1:c.681-220_681-219del	XM_047418854.1:c.681-219del	XM_047418854.1:c.681-219dup	XM_047418854.1:c.681-220_681-219dup	XM_047418854.1:c.681-221_681-219dup	XM_047418854.1:c.681-223_681-219dup	XM_047418854.1:c.681-233_681-219dup	XM_047418854.1:c.681-234_681-219dup	XM_047418854.1:c.681-219_681-218insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA
TUBE1 transcript variant X2	XM_047418855.1:c.588-219=	XM_047418855.1:c.588-224_588-219del	XM_047418855.1:c.588-222_588-219del	XM_047418855.1:c.588-221_588-219del	XM_047418855.1:c.588-220_588-219del	XM_047418855.1:c.588-219del	XM_047418855.1:c.588-219dup	XM_047418855.1:c.588-220_588-219dup	XM_047418855.1:c.588-221_588-219dup	XM_047418855.1:c.588-223_588-219dup	XM_047418855.1:c.588-233_588-219dup	XM_047418855.1:c.588-234_588-219dup	XM_047418855.1:c.588-219_588-218insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

32 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80893254	Oct 12, 2018 (152)
2	HGSV	ss82109777	Oct 12, 2018 (152)
3	SSMP	ss663642052	Apr 09, 2015 (144)
4	1000GENOMES	ss1376012677	Aug 28, 2014 (142)
5	ACPOP	ss3733880721	Jul 13, 2019 (153)
6	KHV_HUMAN_GENOMES	ss3808683076	Jul 13, 2019 (153)
7	EVA	ss3830138011	Apr 26, 2020 (154)
8	KOGIC	ss3959860959	Apr 26, 2020 (154)
9	KOGIC	ss3959860960	Apr 26, 2020 (154)
10	GNOMAD	ss4149335934	Apr 26, 2021 (155)
11	GNOMAD	ss4149335935	Apr 26, 2021 (155)
12	GNOMAD	ss4149335936	Apr 26, 2021 (155)
13	GNOMAD	ss4149335937	Apr 26, 2021 (155)
14	GNOMAD	ss4149335938	Apr 26, 2021 (155)
15	GNOMAD	ss4149335939	Apr 26, 2021 (155)
16	GNOMAD	ss4149335940	Apr 26, 2021 (155)
17	GNOMAD	ss4149335942	Apr 26, 2021 (155)
18	GNOMAD	ss4149335943	Apr 26, 2021 (155)
19	GNOMAD	ss4149335944	Apr 26, 2021 (155)
20	GNOMAD	ss4149335945	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5179404717	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5179404718	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5179404719	Apr 26, 2021 (155)
24	1000G_HIGH_COVERAGE	ss5269940764	Oct 13, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5269940765	Oct 13, 2022 (156)
26	HUGCELL_USP	ss5467421925	Oct 13, 2022 (156)
27	HUGCELL_USP	ss5467421927	Oct 13, 2022 (156)
28	HUGCELL_USP	ss5467421928	Oct 13, 2022 (156)
29	EVA	ss5624159762	Oct 13, 2022 (156)
30	TOMMO_GENOMICS	ss5718145315	Oct 13, 2022 (156)
31	TOMMO_GENOMICS	ss5718145317	Oct 13, 2022 (156)
32	TOMMO_GENOMICS	ss5718145318	Oct 13, 2022 (156)
33	1000Genomes	NC_000006.11 - 112396272	Oct 12, 2018 (152)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237667138 (NC_000006.12:112075068::T 65/96906) Row 237667139 (NC_000006.12:112075068::TT 1/96918) Row 237667140 (NC_000006.12:112075068::TTT 2/96918)...	-	Apr 26, 2021 (155)
45	Korean Genome Project Submission ignored due to conflicting rows: Row 16238960 (NC_000006.12:112075073:T: 665/1802) Row 16238961 (NC_000006.12:112075072:TT: 25/1802)	-	Apr 26, 2020 (154)
46	Korean Genome Project Submission ignored due to conflicting rows: Row 16238960 (NC_000006.12:112075073:T: 665/1802) Row 16238961 (NC_000006.12:112075072:TT: 25/1802)	-	Apr 26, 2020 (154)
47	Northern Sweden	NC_000006.11 - 112396272	Jul 13, 2019 (153)
48	8.3KJPN Submission ignored due to conflicting rows: Row 37374024 (NC_000006.11:112396271:T: 7174/16466) Row 37374025 (NC_000006.11:112396271:TT: 76/16466) Row 37374026 (NC_000006.11:112396271::T 4/16466)	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 37374024 (NC_000006.11:112396271:T: 7174/16466) Row 37374025 (NC_000006.11:112396271:TT: 76/16466) Row 37374026 (NC_000006.11:112396271::T 4/16466)	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 37374024 (NC_000006.11:112396271:T: 7174/16466) Row 37374025 (NC_000006.11:112396271:TT: 76/16466) Row 37374026 (NC_000006.11:112396271::T 4/16466)	-	Apr 26, 2021 (155)
51	14KJPN Submission ignored due to conflicting rows: Row 51982419 (NC_000006.12:112075068:T: 12192/27962) Row 51982421 (NC_000006.12:112075068:TT: 123/27962) Row 51982422 (NC_000006.12:112075068::T 14/27962)	-	Oct 13, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 51982419 (NC_000006.12:112075068:T: 12192/27962) Row 51982421 (NC_000006.12:112075068:TT: 123/27962) Row 51982422 (NC_000006.12:112075068::T 14/27962)	-	Oct 13, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 51982419 (NC_000006.12:112075068:T: 12192/27962) Row 51982421 (NC_000006.12:112075068:TT: 123/27962) Row 51982422 (NC_000006.12:112075068::T 14/27962)	-	Oct 13, 2022 (156)
54	ALFA	NC_000006.12 - 112075069	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
3151722857	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4149335945	NC_000006.12:112075068:TTTT:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4149335944	NC_000006.12:112075068:TTT:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5179404718	NC_000006.11:112396271:TT:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4149335943, ss5269940765, ss5467421927, ss5718145317	NC_000006.12:112075068:TT:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3151722857	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3959860960	NC_000006.12:112075072:TT:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
33657985, 7165586, ss663642052, ss1376012677, ss3733880721, ss3830138011, ss5179404717, ss5624159762	NC_000006.11:112396271:T:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3808683076, ss4149335942, ss5269940764, ss5467421925, ss5718145315	NC_000006.12:112075068:T:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3151722857	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3959860959	NC_000006.12:112075073:T:	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5179404719	NC_000006.11:112396271::T	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4149335934, ss5467421928, ss5718145318	NC_000006.12:112075068::T	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3151722857	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss80893254, ss82109777	NT_025741.15:16565744::T	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4149335935	NC_000006.12:112075068::TT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3151722857	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4149335936	NC_000006.12:112075068::TTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4149335937	NC_000006.12:112075068::TTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4149335938	NC_000006.12:112075068::TTTTTTTTTT… NC_000006.12:112075068::TTTTTTTTTTTTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4149335939	NC_000006.12:112075068::TTTTTTTTTT… NC_000006.12:112075068::TTTTTTTTTTTTTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4149335940	NC_000006.12:112075068::TTTTTTTTTT… NC_000006.12:112075068::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTT	NC_000006.12:112075068:TTTTTTTTTTT… NC_000006.12:112075068:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTT	(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 rs371166684

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

rs371166684