Name: rs1196431061
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.

rs1196431061

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:74365941-74365957 (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)₇ / del(T)₆ / delTTT / delTT…
del(T)₇ / del(T)₆ / delTTT / delTT / delT / dupT / dupTT / dupTTT
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.05465 (720/13175, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PDPR2P : 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	HTRZ	HWEP
Total	Global	13175	TTTTTTTTTTTTTTTTT=0.94095	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.05465, TTTTTTTTTTTTTTTT=0.00296, TTTTTTTTTTTTTTTTTT=0.00137, TTTTTTTTTTTTTTTTTTTT=0.00008, TTTTTTTTTTTTTTTTTTT=0.00000	0.890455	0.109545	12
European	Sub	10277	TTTTTTTTTTTTTTTTT=0.92459	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.06986, TTTTTTTTTTTTTTTT=0.00370, TTTTTTTTTTTTTTTTTT=0.00175, TTTTTTTTTTTTTTTTTTTT=0.00010, TTTTTTTTTTTTTTTTTTT=0.00000	0.859618	0.140382	16
African	Sub	1812	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	N/A
African Others	Sub	68	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
African American	Sub	1744	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	N/A
Asian	Sub	92	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
East Asian	Sub	70	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Latin American 1	Sub	112	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
Latin American 2	Sub	460	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
South Asian	Sub	62	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Other	Sub	360	TTTTTTTTTTTTTTTTT=0.992	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.006, TTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	0.988827	0.011173	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13175	(T)₁₇=0.94095	del(T)₇=0.00000, del(T)₆=0.00000, delTTT=0.00000, delTT=0.05465, delT=0.00296, dupT=0.00137, dupTT=0.00000, dupTTT=0.00008
Allele Frequency Aggregator	European	Sub	10277	(T)₁₇=0.92459	del(T)₇=0.00000, del(T)₆=0.00000, delTTT=0.00000, delTT=0.06986, delT=0.00370, dupT=0.00175, dupTT=0.00000, dupTTT=0.00010
Allele Frequency Aggregator	African	Sub	1812	(T)₁₇=1.0000	del(T)₇=0.0000, del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	460	(T)₁₇=1.000	del(T)₇=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	360	(T)₁₇=0.992	del(T)₇=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.006, delT=0.003, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	112	(T)₁₇=1.000	del(T)₇=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	92	(T)₁₇=1.00	del(T)₇=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	62	(T)₁₇=1.00	del(T)₇=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00

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.74365951_74365957del
GRCh38.p14 chr 16	NC_000016.10:g.74365952_74365957del
GRCh38.p14 chr 16	NC_000016.10:g.74365955_74365957del
GRCh38.p14 chr 16	NC_000016.10:g.74365956_74365957del
GRCh38.p14 chr 16	NC_000016.10:g.74365957del
GRCh38.p14 chr 16	NC_000016.10:g.74365957dup
GRCh38.p14 chr 16	NC_000016.10:g.74365956_74365957dup
GRCh38.p14 chr 16	NC_000016.10:g.74365955_74365957dup
GRCh37.p13 chr 16	NC_000016.9:g.74399849_74399855del
GRCh37.p13 chr 16	NC_000016.9:g.74399850_74399855del
GRCh37.p13 chr 16	NC_000016.9:g.74399853_74399855del
GRCh37.p13 chr 16	NC_000016.9:g.74399854_74399855del
GRCh37.p13 chr 16	NC_000016.9:g.74399855del
GRCh37.p13 chr 16	NC_000016.9:g.74399855dup
GRCh37.p13 chr 16	NC_000016.9:g.74399854_74399855dup
GRCh37.p13 chr 16	NC_000016.9:g.74399853_74399855dup

Gene: PDPR2P, pyruvate dehydrogenase phosphatase regulatory subunit 2, pseudogene (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PDPR2P transcript	NR_026950.1:n.	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)₁₇=	del(T)₇	del(T)₆	delTTT	delTT	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 16	NC_000016.10:g.74365941_74365957=	NC_000016.10:g.74365951_74365957del	NC_000016.10:g.74365952_74365957del	NC_000016.10:g.74365955_74365957del	NC_000016.10:g.74365956_74365957del	NC_000016.10:g.74365957del	NC_000016.10:g.74365957dup	NC_000016.10:g.74365956_74365957dup	NC_000016.10:g.74365955_74365957dup
GRCh37.p13 chr 16	NC_000016.9:g.74399839_74399855=	NC_000016.9:g.74399849_74399855del	NC_000016.9:g.74399850_74399855del	NC_000016.9:g.74399853_74399855del	NC_000016.9:g.74399854_74399855del	NC_000016.9:g.74399855del	NC_000016.9:g.74399855dup	NC_000016.9:g.74399854_74399855dup	NC_000016.9:g.74399853_74399855dup

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#.

27 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3014774267	Nov 08, 2017 (151)
2	EVA_DECODE	ss3699577548	Jul 13, 2019 (153)
3	EVA_DECODE	ss3699577549	Jul 13, 2019 (153)
4	EVA_DECODE	ss3699577550	Jul 13, 2019 (153)
5	ACPOP	ss3741644575	Jul 13, 2019 (153)
6	ACPOP	ss3741644576	Jul 13, 2019 (153)
7	PACBIO	ss3788080121	Jul 13, 2019 (153)
8	KOGIC	ss3977905026	Apr 27, 2020 (154)
9	KOGIC	ss3977905027	Apr 27, 2020 (154)
10	KOGIC	ss3977905028	Apr 27, 2020 (154)
11	GNOMAD	ss4303847037	Apr 26, 2021 (155)
12	GNOMAD	ss4303847038	Apr 26, 2021 (155)
13	GNOMAD	ss4303847039	Apr 26, 2021 (155)
14	GNOMAD	ss4303847041	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5220320431	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5220320432	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5220320433	Apr 26, 2021 (155)
18	1000G_HIGH_COVERAGE	ss5301517319	Oct 16, 2022 (156)
19	1000G_HIGH_COVERAGE	ss5301517320	Oct 16, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5301517321	Oct 16, 2022 (156)
21	1000G_HIGH_COVERAGE	ss5301517323	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5494804896	Oct 16, 2022 (156)
23	HUGCELL_USP	ss5494804897	Oct 16, 2022 (156)
24	HUGCELL_USP	ss5494804898	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5775550684	Oct 16, 2022 (156)
26	TOMMO_GENOMICS	ss5775550685	Oct 16, 2022 (156)
27	TOMMO_GENOMICS	ss5775550686	Oct 16, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 494317560 (NC_000016.10:74365940::T 1381/135070) Row 494317561 (NC_000016.10:74365940::TT 24/135170) Row 494317562 (NC_000016.10:74365940::TTT 2/135210)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 494317560 (NC_000016.10:74365940::T 1381/135070) Row 494317561 (NC_000016.10:74365940::TT 24/135170) Row 494317562 (NC_000016.10:74365940::TTT 2/135210)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 494317560 (NC_000016.10:74365940::T 1381/135070) Row 494317561 (NC_000016.10:74365940::TT 24/135170) Row 494317562 (NC_000016.10:74365940::TTT 2/135210)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 494317560 (NC_000016.10:74365940::T 1381/135070) Row 494317561 (NC_000016.10:74365940::TT 24/135170) Row 494317562 (NC_000016.10:74365940::TTT 2/135210)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 494317560 (NC_000016.10:74365940::T 1381/135070) Row 494317561 (NC_000016.10:74365940::TT 24/135170) Row 494317562 (NC_000016.10:74365940::TTT 2/135210)...	-	Apr 26, 2021 (155)
33	Korean Genome Project Submission ignored due to conflicting rows: Row 34283027 (NC_000016.10:74365940:TT: 186/1832) Row 34283028 (NC_000016.10:74365941:T: 139/1832) Row 34283029 (NC_000016.10:74365942::T 146/1832)	-	Apr 27, 2020 (154)
34	Korean Genome Project Submission ignored due to conflicting rows: Row 34283027 (NC_000016.10:74365940:TT: 186/1832) Row 34283028 (NC_000016.10:74365941:T: 139/1832) Row 34283029 (NC_000016.10:74365942::T 146/1832)	-	Apr 27, 2020 (154)
35	Korean Genome Project Submission ignored due to conflicting rows: Row 34283027 (NC_000016.10:74365940:TT: 186/1832) Row 34283028 (NC_000016.10:74365941:T: 139/1832) Row 34283029 (NC_000016.10:74365942::T 146/1832)	-	Apr 27, 2020 (154)
36	Northern Sweden Submission ignored due to conflicting rows: Row 14929440 (NC_000016.9:74399838:TT: 80/600) Row 14929441 (NC_000016.9:74399838:T: 5/600)	-	Jul 13, 2019 (153)
37	Northern Sweden Submission ignored due to conflicting rows: Row 14929440 (NC_000016.9:74399838:TT: 80/600) Row 14929441 (NC_000016.9:74399838:T: 5/600)	-	Jul 13, 2019 (153)
38	8.3KJPN Submission ignored due to conflicting rows: Row 78289738 (NC_000016.9:74399838:TT: 1212/16760) Row 78289739 (NC_000016.9:74399838:T: 86/16760) Row 78289740 (NC_000016.9:74399838::T 35/16760)	-	Apr 26, 2021 (155)
39	8.3KJPN Submission ignored due to conflicting rows: Row 78289738 (NC_000016.9:74399838:TT: 1212/16760) Row 78289739 (NC_000016.9:74399838:T: 86/16760) Row 78289740 (NC_000016.9:74399838::T 35/16760)	-	Apr 26, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 78289738 (NC_000016.9:74399838:TT: 1212/16760) Row 78289739 (NC_000016.9:74399838:T: 86/16760) Row 78289740 (NC_000016.9:74399838::T 35/16760)	-	Apr 26, 2021 (155)
41	14KJPN Submission ignored due to conflicting rows: Row 109387788 (NC_000016.10:74365940:TT: 2061/28258) Row 109387789 (NC_000016.10:74365940:T: 145/28258) Row 109387790 (NC_000016.10:74365940::T 47/28258)	-	Oct 16, 2022 (156)
42	14KJPN Submission ignored due to conflicting rows: Row 109387788 (NC_000016.10:74365940:TT: 2061/28258) Row 109387789 (NC_000016.10:74365940:T: 145/28258) Row 109387790 (NC_000016.10:74365940::T 47/28258)	-	Oct 16, 2022 (156)
43	14KJPN Submission ignored due to conflicting rows: Row 109387788 (NC_000016.10:74365940:TT: 2061/28258) Row 109387789 (NC_000016.10:74365940:T: 145/28258) Row 109387790 (NC_000016.10:74365940::T 47/28258)	-	Oct 16, 2022 (156)
44	ALFA	NC_000016.10 - 74365941	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
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4303847041, ss5301517323	NC_000016.10:74365940:TTT:	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3014774267, ss3741644575, ss5220320431	NC_000016.9:74399838:TT:	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3699577548, ss3977905026, ss5301517319, ss5494804898, ss5775550684	NC_000016.10:74365940:TT:	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3741644576, ss3788080121, ss5220320432	NC_000016.9:74399838:T:	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5301517320, ss5494804896, ss5775550685	NC_000016.10:74365940:T:	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3699577549, ss3977905027	NC_000016.10:74365941:T:	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5220320433	NC_000016.9:74399838::T	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4303847037, ss5301517321, ss5494804897, ss5775550686	NC_000016.10:74365940::T	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3699577550, ss3977905028	NC_000016.10:74365942::T	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4303847038	NC_000016.10:74365940::TT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4303847039	NC_000016.10:74365940::TTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10292575376	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000016.10:74365940:TTTTTTTTTTTT… NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(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 rs1196431061

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

rs1196431061