Name: rs113928658
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.

rs113928658

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:132588454-132588467 (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(TA)₅ / delTA / dupTA / insTACG…
del(TA)₅ / delTA / dupTA / insTACGTGT(AT)₄ACG(TA)₈ / dupTATA / dup(TA)₃ / dup(TA)₇
Variation Type: Indel Insertion and Deletion
Frequency: dupTA=0.07465 (896/12002, ALFA)
dupTA=0.1827 (915/5008, 1000G)
dupTA=0.188 (113/600, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TAAR5 : 500B Downstream 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	12002	TATATATATATATA=0.92535	TATA=0.00000, TATATATATATA=0.00000, TATATATATATATATA=0.07465, TATATATATATATATATA=0.00000, TATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATA=0.00000	0.865022	0.014331	0.120647	32
European	Sub	9402	TATATATATATATA=0.9048	TATA=0.0000, TATATATATATA=0.0000, TATATATATATATATA=0.0952, TATATATATATATATATA=0.0000, TATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATA=0.0000	0.827909	0.018294	0.153797	29
African	Sub	1788	TATATATATATATA=1.0000	TATA=0.0000, TATATATATATA=0.0000, TATATATATATATATA=0.0000, TATATATATATATATATA=0.0000, TATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	66	TATATATATATATA=1.00	TATA=0.00, TATATATATATA=0.00, TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1722	TATATATATATATA=1.0000	TATA=0.0000, TATATATATATA=0.0000, TATATATATATATATA=0.0000, TATATATATATATATATA=0.0000, TATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	82	TATATATATATATA=1.00	TATA=0.00, TATATATATATA=0.00, TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	64	TATATATATATATA=1.00	TATA=0.00, TATATATATATA=0.00, TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TATATATATATATA=1.00	TATA=0.00, TATATATATATA=0.00, TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	88	TATATATATATATA=1.00	TATA=0.00, TATATATATATA=0.00, TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	306	TATATATATATATA=1.000	TATA=0.000, TATATATATATA=0.000, TATATATATATATATA=0.000, TATATATATATATATATA=0.000, TATATATATATATATATATA=0.000, TATATATATATATATATATATATATATA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	56	TATATATATATATA=1.00	TATA=0.00, TATATATATATA=0.00, TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
Other	Sub	280	TATATATATATATA=0.996	TATA=0.000, TATATATATATA=0.000, TATATATATATATATA=0.004, TATATATATATATATATA=0.000, TATATATATATATATATATA=0.000, TATATATATATATATATATATATATATA=0.000	0.992857	0.0	0.007143	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	12002	(TA)₇=0.92535	del(TA)₅=0.00000, delTA=0.00000, dupTA=0.07465, dupTATA=0.00000, dup(TA)₃=0.00000, dup(TA)₇=0.00000
Allele Frequency Aggregator	European	Sub	9402	(TA)₇=0.9048	del(TA)₅=0.0000, delTA=0.0000, dupTA=0.0952, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₇=0.0000
Allele Frequency Aggregator	African	Sub	1788	(TA)₇=1.0000	del(TA)₅=0.0000, delTA=0.0000, dupTA=0.0000, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	306	(TA)₇=1.000	del(TA)₅=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₇=0.000
Allele Frequency Aggregator	Other	Sub	280	(TA)₇=0.996	del(TA)₅=0.000, delTA=0.000, dupTA=0.004, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	88	(TA)₇=1.00	del(TA)₅=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₇=0.00
Allele Frequency Aggregator	Asian	Sub	82	(TA)₇=1.00	del(TA)₅=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	56	(TA)₇=1.00	del(TA)₅=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₇=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupTA=0.1827
1000Genomes	African	Sub	1322	- No frequency provided	dupTA=0.1641
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupTA=0.1716
1000Genomes	Europe	Sub	1006	- No frequency provided	dupTA=0.2018
1000Genomes	South Asian	Sub	978	- No frequency provided	dupTA=0.134
1000Genomes	American	Sub	694	- No frequency provided	dupTA=0.275
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupTA=0.188

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.132588454TA[2]
GRCh38.p14 chr 6	NC_000006.12:g.132588454TA[6]
GRCh38.p14 chr 6	NC_000006.12:g.132588454TA[8]
GRCh38.p14 chr 6	NC_000006.12:g.132588454_132588467TA[8]CGTGTATATATATACGTATATATATATATATA[1]
GRCh38.p14 chr 6	NC_000006.12:g.132588454TA[9]
GRCh38.p14 chr 6	NC_000006.12:g.132588454TA[10]
GRCh38.p14 chr 6	NC_000006.12:g.132588454TA[14]
GRCh37.p13 chr 6	NC_000006.11:g.132909593TA[2]
GRCh37.p13 chr 6	NC_000006.11:g.132909593TA[6]
GRCh37.p13 chr 6	NC_000006.11:g.132909593TA[8]
GRCh37.p13 chr 6	NC_000006.11:g.132909593_132909606TA[8]CGTGTATATATATACGTATATATATATATATA[1]
GRCh37.p13 chr 6	NC_000006.11:g.132909593TA[9]
GRCh37.p13 chr 6	NC_000006.11:g.132909593TA[10]
GRCh37.p13 chr 6	NC_000006.11:g.132909593TA[14]

Gene: TAAR5, trace amine associated receptor 5 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TAAR5 transcript variant 2	NM_001389527.1:c.	N/A	Downstream Transcript Variant
TAAR5 transcript variant 1	NM_003967.3:c.	N/A	Downstream 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	(TA)₇=	del(TA)₅	delTA	dupTA	insTACGTGT(AT)₄ACG(TA)₈	dupTATA	dup(TA)₃	dup(TA)₇
GRCh38.p14 chr 6	NC_000006.12:g.132588454_132588467=	NC_000006.12:g.132588454TA[2]	NC_000006.12:g.132588454TA[6]	NC_000006.12:g.132588454TA[8]	NC_000006.12:g.132588454_132588467TA[8]CGTGTATATATATACGTATATATATATATATA[1]	NC_000006.12:g.132588454TA[9]	NC_000006.12:g.132588454TA[10]	NC_000006.12:g.132588454TA[14]
GRCh37.p13 chr 6	NC_000006.11:g.132909593_132909606=	NC_000006.11:g.132909593TA[2]	NC_000006.11:g.132909593TA[6]	NC_000006.11:g.132909593TA[8]	NC_000006.11:g.132909593_132909606TA[8]CGTGTATATATATACGTATATATATATATATA[1]	NC_000006.11:g.132909593TA[9]	NC_000006.11:g.132909593TA[10]	NC_000006.11:g.132909593TA[14]

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#.

46 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42756041	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95442887	Oct 12, 2018 (152)
3	BUSHMAN	ss193887721	Jul 04, 2010 (132)
4	LUNTER	ss553270560	Apr 25, 2013 (138)
5	SSMP	ss663653826	Apr 01, 2015 (144)
6	1000GENOMES	ss1376214859	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1705374451	Oct 12, 2018 (152)
8	EVA_UK10K_TWINSUK	ss1705374492	Oct 12, 2018 (152)
9	EVA_UK10K_ALSPAC	ss1710294568	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710294623	Apr 01, 2015 (144)
11	JJLAB	ss2030797672	Sep 14, 2016 (149)
12	SWEGEN	ss2999987492	Jan 10, 2018 (151)
13	MCHAISSO	ss3065106988	Jan 10, 2018 (151)
14	URBANLAB	ss3648476556	Oct 12, 2018 (152)
15	EVA_DECODE	ss3718321404	Jul 13, 2019 (153)
16	EVA_DECODE	ss3718321405	Jul 13, 2019 (153)
17	EVA_DECODE	ss3718321406	Jul 13, 2019 (153)
18	ACPOP	ss3734003160	Jul 13, 2019 (153)
19	KHV_HUMAN_GENOMES	ss3808854078	Jul 13, 2019 (153)
20	EVA	ss3830203724	Apr 26, 2020 (154)
21	EVA	ss3838589748	Apr 26, 2020 (154)
22	EVA	ss3844039830	Apr 26, 2020 (154)
23	GNOMAD	ss4151806958	Apr 26, 2021 (155)
24	GNOMAD	ss4151806959	Apr 26, 2021 (155)
25	GNOMAD	ss4151806960	Apr 26, 2021 (155)
26	GNOMAD	ss4151806961	Apr 26, 2021 (155)
27	GNOMAD	ss4151806962	Apr 26, 2021 (155)
28	GNOMAD	ss4151806963	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5180032336	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5180032337	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5180032338	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5270428364	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5270428365	Oct 13, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5270428366	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5467862850	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5467862851	Oct 13, 2022 (156)
37	EVA	ss5508717345	Oct 13, 2022 (156)
38	EVA	ss5624160539	Oct 13, 2022 (156)
39	EVA	ss5624160540	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5718944740	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5718944741	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5718944742	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5718944743	Oct 13, 2022 (156)
44	EVA	ss5843019432	Oct 13, 2022 (156)
45	EVA	ss5843019433	Oct 13, 2022 (156)
46	EVA	ss5855592316	Oct 13, 2022 (156)
47	1000Genomes	NC_000006.11 - 132909593	Oct 12, 2018 (152)
48	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19078352 (NC_000006.11:132909592::TA 704/3854) Row 19078353 (NC_000006.11:132909592:TA: 143/3854)	-	Oct 12, 2018 (152)
49	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19078352 (NC_000006.11:132909592::TA 704/3854) Row 19078353 (NC_000006.11:132909592:TA: 143/3854)	-	Oct 12, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 241770800 (NC_000006.12:132588453::TA 25850/136046) Row 241770801 (NC_000006.12:132588453::TATA 1629/136242) Row 241770802 (NC_000006.12:132588453::TATATA 155/136248)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 241770800 (NC_000006.12:132588453::TA 25850/136046) Row 241770801 (NC_000006.12:132588453::TATA 1629/136242) Row 241770802 (NC_000006.12:132588453::TATATA 155/136248)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 241770800 (NC_000006.12:132588453::TA 25850/136046) Row 241770801 (NC_000006.12:132588453::TATA 1629/136242) Row 241770802 (NC_000006.12:132588453::TATATA 155/136248)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 241770800 (NC_000006.12:132588453::TA 25850/136046) Row 241770801 (NC_000006.12:132588453::TATA 1629/136242) Row 241770802 (NC_000006.12:132588453::TATATA 155/136248)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 241770800 (NC_000006.12:132588453::TA 25850/136046) Row 241770801 (NC_000006.12:132588453::TATA 1629/136242) Row 241770802 (NC_000006.12:132588453::TATATA 155/136248)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 241770800 (NC_000006.12:132588453::TA 25850/136046) Row 241770801 (NC_000006.12:132588453::TATA 1629/136242) Row 241770802 (NC_000006.12:132588453::TATATA 155/136248)...	-	Apr 26, 2021 (155)
56	Northern Sweden	NC_000006.11 - 132909593	Jul 13, 2019 (153)
57	8.3KJPN Submission ignored due to conflicting rows: Row 38001643 (NC_000006.11:132909592::TA 2360/16760) Row 38001644 (NC_000006.11:132909592::TATA 20/16760) Row 38001645 (NC_000006.11:132909592::TATATA 2/16760)	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 38001643 (NC_000006.11:132909592::TA 2360/16760) Row 38001644 (NC_000006.11:132909592::TATA 20/16760) Row 38001645 (NC_000006.11:132909592::TATATA 2/16760)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 38001643 (NC_000006.11:132909592::TA 2360/16760) Row 38001644 (NC_000006.11:132909592::TATA 20/16760) Row 38001645 (NC_000006.11:132909592::TATATA 2/16760)	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 52781844 (NC_000006.12:132588453::TA 3897/28258) Row 52781845 (NC_000006.12:132588453:TA: 3/28258) Row 52781846 (NC_000006.12:132588453::TATA 32/28258)...	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 52781844 (NC_000006.12:132588453::TA 3897/28258) Row 52781845 (NC_000006.12:132588453:TA: 3/28258) Row 52781846 (NC_000006.12:132588453::TATA 32/28258)...	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 52781844 (NC_000006.12:132588453::TA 3897/28258) Row 52781845 (NC_000006.12:132588453:TA: 3/28258) Row 52781846 (NC_000006.12:132588453::TATA 32/28258)...	-	Oct 13, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 52781844 (NC_000006.12:132588453::TA 3897/28258) Row 52781845 (NC_000006.12:132588453:TA: 3/28258) Row 52781846 (NC_000006.12:132588453::TATA 32/28258)...	-	Oct 13, 2022 (156)
64	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19078352 (NC_000006.11:132909592::TA 633/3708) Row 19078353 (NC_000006.11:132909592:TA: 94/3708)	-	Oct 12, 2018 (152)
65	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19078352 (NC_000006.11:132909592::TA 633/3708) Row 19078353 (NC_000006.11:132909592:TA: 94/3708)	-	Oct 12, 2018 (152)
66	ALFA	NC_000006.12 - 132588454	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
1856068331	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATA	(self)
ss1705374451, ss1705374492, ss5508717345, ss5624160539, ss5843019433	NC_000006.11:132909592:TA:	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATA	(self)
ss3718321404, ss4151806963, ss5718944741	NC_000006.12:132588453:TA:	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATA	(self)
1856068331	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATA	(self)
ss553270560	NC_000006.10:132951285::TA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
34234535, 7288025, ss663653826, ss1376214859, ss2030797672, ss2999987492, ss3734003160, ss3830203724, ss3838589748, ss5180032336, ss5624160540, ss5843019432	NC_000006.11:132909592::TA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
ss1710294568, ss1710294623	NC_000006.11:132909594::TA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
ss3065106988, ss3648476556, ss3808854078, ss3844039830, ss4151806958, ss5270428364, ss5467862850, ss5718944740, ss5855592316	NC_000006.12:132588453::TA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
1856068331	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
ss3718321405	NC_000006.12:132588455::TA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
ss42756041, ss95442887	NT_025741.15:37079063::TA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
ss193887721	NT_025741.16:72358519::TA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATA	(self)
ss4151806962	NC_000006.12:132588453::TATATATATA… NC_000006.12:132588453::TATATATATATATATACGTGTATATATATACGTA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATACGTGTATATATATACGTATATATATATATATA	(self)
ss5180032337	NC_000006.11:132909592::TATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATA	(self)
ss4151806959, ss5270428365, ss5467862851, ss5718944742	NC_000006.12:132588453::TATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATA	(self)
1856068331	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATA	(self)
ss3718321406	NC_000006.12:132588455::TATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATA	(self)
ss5180032338	NC_000006.11:132909592::TATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATATA	(self)
ss4151806960, ss5270428366, ss5718944743	NC_000006.12:132588453::TATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATATA	(self)
1856068331	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATATA	(self)
ss4151806961	NC_000006.12:132588453::TATATATATA… NC_000006.12:132588453::TATATATATATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATATATATATATA	(self)
1856068331	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATATATATATATA	NC_000006.12:132588453:TATATATATAT… NC_000006.12:132588453:TATATATATATATA:TATATATATATATATATATATATATATA	(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 rs113928658

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

rs113928658