Name: rs147569014
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.

rs147569014

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:3711033-3711046 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.4499 (2253/5008, 1000G)
delAA=0.0000 (0/2764, ALFA)
delA=0.0000 (0/2764, ALFA) (+ 4 more)
dupA=0.0000 (0/2764, ALFA)
dupAA=0.0000 (0/2764, ALFA)
dupAAA=0.0000 (0/2764, ALFA)
dup(A)₄=0.0000 (0/2764, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRAP1 : 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	2764	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2138	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	342	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	16	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	326	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	30	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	26	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	36	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	134	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	78	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	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
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.4499
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.5106
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.3938
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.3618
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.497
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.477
Allele Frequency Aggregator	Total	Global	2764	(A)₁₄=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	2138	(A)₁₄=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	342	(A)₁₄=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	134	(A)₁₄=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	78	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	36	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	30	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	6	(A)₁₄=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0

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 16	NC_000016.10:g.3711044_3711046del
GRCh38.p14 chr 16	NC_000016.10:g.3711045_3711046del
GRCh38.p14 chr 16	NC_000016.10:g.3711046del
GRCh38.p14 chr 16	NC_000016.10:g.3711046dup
GRCh38.p14 chr 16	NC_000016.10:g.3711045_3711046dup
GRCh38.p14 chr 16	NC_000016.10:g.3711044_3711046dup
GRCh38.p14 chr 16	NC_000016.10:g.3711043_3711046dup
GRCh37.p13 chr 16	NC_000016.9:g.3761045_3761047del
GRCh37.p13 chr 16	NC_000016.9:g.3761046_3761047del
GRCh37.p13 chr 16	NC_000016.9:g.3761047del
GRCh37.p13 chr 16	NC_000016.9:g.3761047dup
GRCh37.p13 chr 16	NC_000016.9:g.3761046_3761047dup
GRCh37.p13 chr 16	NC_000016.9:g.3761045_3761047dup
GRCh37.p13 chr 16	NC_000016.9:g.3761044_3761047dup
TRAP1 RefSeqGene	NG_033088.1:g.11563_11565del
TRAP1 RefSeqGene	NG_033088.1:g.11564_11565del
TRAP1 RefSeqGene	NG_033088.1:g.11565del
TRAP1 RefSeqGene	NG_033088.1:g.11565dup
TRAP1 RefSeqGene	NG_033088.1:g.11564_11565dup
TRAP1 RefSeqGene	NG_033088.1:g.11563_11565dup
TRAP1 RefSeqGene	NG_033088.1:g.11562_11565dup

Gene: TRAP1, TNF receptor associated protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TRAP1 transcript variant 2	NM_001272049.2:c.88+6386_… NM_001272049.2:c.88+6386_88+6388del	N/A	Intron Variant
TRAP1 transcript variant 1	NM_016292.3:c.88+6386_88+… NM_016292.3:c.88+6386_88+6388del	N/A	Intron Variant
TRAP1 transcript variant X1	XM_011522345.3:c.	N/A	Genic 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	(A)₁₄=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 16	NC_000016.10:g.3711033_3711046=	NC_000016.10:g.3711044_3711046del	NC_000016.10:g.3711045_3711046del	NC_000016.10:g.3711046del	NC_000016.10:g.3711046dup	NC_000016.10:g.3711045_3711046dup	NC_000016.10:g.3711044_3711046dup	NC_000016.10:g.3711043_3711046dup
GRCh37.p13 chr 16	NC_000016.9:g.3761034_3761047=	NC_000016.9:g.3761045_3761047del	NC_000016.9:g.3761046_3761047del	NC_000016.9:g.3761047del	NC_000016.9:g.3761047dup	NC_000016.9:g.3761046_3761047dup	NC_000016.9:g.3761045_3761047dup	NC_000016.9:g.3761044_3761047dup
TRAP1 RefSeqGene	NG_033088.1:g.11552_11565=	NG_033088.1:g.11563_11565del	NG_033088.1:g.11564_11565del	NG_033088.1:g.11565del	NG_033088.1:g.11565dup	NG_033088.1:g.11564_11565dup	NG_033088.1:g.11563_11565dup	NG_033088.1:g.11562_11565dup
TRAP1 transcript variant 2	NM_001272049.1:c.88+6388=	NM_001272049.1:c.88+6386_88+6388del	NM_001272049.1:c.88+6387_88+6388del	NM_001272049.1:c.88+6388del	NM_001272049.1:c.88+6388dup	NM_001272049.1:c.88+6387_88+6388dup	NM_001272049.1:c.88+6386_88+6388dup	NM_001272049.1:c.88+6385_88+6388dup
TRAP1 transcript variant 2	NM_001272049.2:c.88+6388=	NM_001272049.2:c.88+6386_88+6388del	NM_001272049.2:c.88+6387_88+6388del	NM_001272049.2:c.88+6388del	NM_001272049.2:c.88+6388dup	NM_001272049.2:c.88+6387_88+6388dup	NM_001272049.2:c.88+6386_88+6388dup	NM_001272049.2:c.88+6385_88+6388dup
TRAP1 transcript variant 1	NM_016292.2:c.88+6388=	NM_016292.2:c.88+6386_88+6388del	NM_016292.2:c.88+6387_88+6388del	NM_016292.2:c.88+6388del	NM_016292.2:c.88+6388dup	NM_016292.2:c.88+6387_88+6388dup	NM_016292.2:c.88+6386_88+6388dup	NM_016292.2:c.88+6385_88+6388dup
TRAP1 transcript variant 1	NM_016292.3:c.88+6388=	NM_016292.3:c.88+6386_88+6388del	NM_016292.3:c.88+6387_88+6388del	NM_016292.3:c.88+6388del	NM_016292.3:c.88+6388dup	NM_016292.3:c.88+6387_88+6388dup	NM_016292.3:c.88+6386_88+6388dup	NM_016292.3:c.88+6385_88+6388dup

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#.

33 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294878023	May 09, 2011 (134)
2	SSMP	ss664313666	Apr 01, 2015 (144)
3	1000GENOMES	ss1375478148	Aug 21, 2014 (142)
4	HAMMER_LAB	ss1808385403	Sep 08, 2015 (146)
5	SWEGEN	ss3013951642	Nov 08, 2017 (151)
6	PACBIO	ss3787960784	Jul 13, 2019 (153)
7	KHV_HUMAN_GENOMES	ss3818894397	Jul 13, 2019 (153)
8	EVA	ss3834437430	Apr 27, 2020 (154)
9	EVA	ss3846313622	Apr 27, 2020 (154)
10	KOGIC	ss3976983376	Apr 27, 2020 (154)
11	KOGIC	ss3976983377	Apr 27, 2020 (154)
12	KOGIC	ss3976983378	Apr 27, 2020 (154)
13	GNOMAD	ss4295755637	Apr 27, 2021 (155)
14	GNOMAD	ss4295755638	Apr 27, 2021 (155)
15	GNOMAD	ss4295755639	Apr 27, 2021 (155)
16	GNOMAD	ss4295755641	Apr 27, 2021 (155)
17	GNOMAD	ss4295755642	Apr 27, 2021 (155)
18	GNOMAD	ss4295755643	Apr 27, 2021 (155)
19	TOMMO_GENOMICS	ss5218103080	Apr 27, 2021 (155)
20	TOMMO_GENOMICS	ss5218103081	Apr 27, 2021 (155)
21	TOMMO_GENOMICS	ss5218103082	Apr 27, 2021 (155)
22	1000G_HIGH_COVERAGE	ss5299883309	Oct 17, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5299883310	Oct 17, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5299883311	Oct 17, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5299883312	Oct 17, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5299883313	Oct 17, 2022 (156)
27	HUGCELL_USP	ss5493436422	Oct 17, 2022 (156)
28	HUGCELL_USP	ss5493436423	Oct 17, 2022 (156)
29	HUGCELL_USP	ss5493436424	Oct 17, 2022 (156)
30	TOMMO_GENOMICS	ss5772488572	Oct 17, 2022 (156)
31	TOMMO_GENOMICS	ss5772488573	Oct 17, 2022 (156)
32	TOMMO_GENOMICS	ss5772488574	Oct 17, 2022 (156)
33	EVA	ss5897997710	Oct 17, 2022 (156)
34	1000Genomes	NC_000016.9 - 3761034	Oct 12, 2018 (152)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480828638 (NC_000016.10:3711032::A 63334/122728) Row 480828639 (NC_000016.10:3711032::AA 82/122850) Row 480828640 (NC_000016.10:3711032::AAA 2/122868)...	-	Apr 27, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480828638 (NC_000016.10:3711032::A 63334/122728) Row 480828639 (NC_000016.10:3711032::AA 82/122850) Row 480828640 (NC_000016.10:3711032::AAA 2/122868)...	-	Apr 27, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480828638 (NC_000016.10:3711032::A 63334/122728) Row 480828639 (NC_000016.10:3711032::AA 82/122850) Row 480828640 (NC_000016.10:3711032::AAA 2/122868)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480828638 (NC_000016.10:3711032::A 63334/122728) Row 480828639 (NC_000016.10:3711032::AA 82/122850) Row 480828640 (NC_000016.10:3711032::AAA 2/122868)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480828638 (NC_000016.10:3711032::A 63334/122728) Row 480828639 (NC_000016.10:3711032::AA 82/122850) Row 480828640 (NC_000016.10:3711032::AAA 2/122868)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 480828638 (NC_000016.10:3711032::A 63334/122728) Row 480828639 (NC_000016.10:3711032::AA 82/122850) Row 480828640 (NC_000016.10:3711032::AAA 2/122868)...	-	Apr 27, 2021 (155)
41	Korean Genome Project Submission ignored due to conflicting rows: Row 33361377 (NC_000016.10:3711033::A 770/1826) Row 33361378 (NC_000016.10:3711032:A: 89/1826) Row 33361379 (NC_000016.10:3711033::AA 27/1826)	-	Apr 27, 2020 (154)
42	Korean Genome Project Submission ignored due to conflicting rows: Row 33361377 (NC_000016.10:3711033::A 770/1826) Row 33361378 (NC_000016.10:3711032:A: 89/1826) Row 33361379 (NC_000016.10:3711033::AA 27/1826)	-	Apr 27, 2020 (154)
43	Korean Genome Project Submission ignored due to conflicting rows: Row 33361377 (NC_000016.10:3711033::A 770/1826) Row 33361378 (NC_000016.10:3711032:A: 89/1826) Row 33361379 (NC_000016.10:3711033::AA 27/1826)	-	Apr 27, 2020 (154)
44	8.3KJPN Submission ignored due to conflicting rows: Row 76072387 (NC_000016.9:3761033:A: 665/16738) Row 76072388 (NC_000016.9:3761033::A 6323/16738) Row 76072389 (NC_000016.9:3761033::AA 4/16738)	-	Apr 27, 2021 (155)
45	8.3KJPN Submission ignored due to conflicting rows: Row 76072387 (NC_000016.9:3761033:A: 665/16738) Row 76072388 (NC_000016.9:3761033::A 6323/16738) Row 76072389 (NC_000016.9:3761033::AA 4/16738)	-	Apr 27, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 76072387 (NC_000016.9:3761033:A: 665/16738) Row 76072388 (NC_000016.9:3761033::A 6323/16738) Row 76072389 (NC_000016.9:3761033::AA 4/16738)	-	Apr 27, 2021 (155)
47	14KJPN Submission ignored due to conflicting rows: Row 106325676 (NC_000016.10:3711032:A: 1168/28258) Row 106325677 (NC_000016.10:3711032::A 10786/28258) Row 106325678 (NC_000016.10:3711032::AA 7/28258)	-	Oct 17, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 106325676 (NC_000016.10:3711032:A: 1168/28258) Row 106325677 (NC_000016.10:3711032::A 10786/28258) Row 106325678 (NC_000016.10:3711032::AA 7/28258)	-	Oct 17, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 106325676 (NC_000016.10:3711032:A: 1168/28258) Row 106325677 (NC_000016.10:3711032::A 10786/28258) Row 106325678 (NC_000016.10:3711032::AA 7/28258)	-	Oct 17, 2022 (156)
50	ALFA	NC_000016.10 - 3711033	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
ss4295755643	NC_000016.10:3711032:AAA:	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4295755642, ss5299883311, ss5493436424	NC_000016.10:3711032:AA:	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
5429686394	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3013951642, ss3787960784, ss5218103080	NC_000016.9:3761033:A:	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3976983377, ss4295755641, ss5299883310, ss5493436422, ss5772488572	NC_000016.10:3711032:A:	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
5429686394	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss294878023	NC_000016.8:3701041::A	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
68221548, ss664313666, ss1375478148, ss1808385403, ss3834437430, ss5218103081	NC_000016.9:3761033::A	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3818894397, ss3846313622, ss4295755637, ss5299883309, ss5493436423, ss5772488573, ss5897997710	NC_000016.10:3711032::A	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5429686394	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3976983376	NC_000016.10:3711033::A	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5218103082	NC_000016.9:3761033::AA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4295755638, ss5299883312, ss5772488574	NC_000016.10:3711032::AA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5429686394	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3976983378	NC_000016.10:3711033::AA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4295755639, ss5299883313	NC_000016.10:3711032::AAA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
5429686394	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
5429686394	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:3711032:AAAAAAAAAAAAA… NC_000016.10:3711032:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(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 rs147569014

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

rs147569014