Name: rs34351264
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.

rs34351264

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:48470684-48470692 (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: delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.06309 (693/10984, ALFA)
delT=0.3122 (1461/4680, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C12orf54 : Intron Variant
ANP32D : 2KB Upstream 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	10984	TTTTTTTTT=0.88802	TTTTTTTT=0.04889, TTTTTTTTTT=0.06309, TTTTTTTTTTT=0.00000	0.889023	0.009231	0.101746	26
European	Sub	8594	TTTTTTTTT=0.8573	TTTTTTTT=0.0621, TTTTTTTTTT=0.0805, TTTTTTTTTTT=0.0000	0.854128	0.012134	0.133738	14
African	Sub	1806	TTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	64	TTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1742	TTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	12	TTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	12	TTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	88	TTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	176	TTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	70	TTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	238	TTTTTTTTT=0.983	TTTTTTTT=0.013, TTTTTTTTTT=0.004, TTTTTTTTTTT=0.000	1.0	0.0	0.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10984	(T)₉=0.88802	delT=0.04889, dupT=0.06309, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	8594	(T)₉=0.8573	delT=0.0621, dupT=0.0805, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1806	(T)₉=1.0000	delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Other	Sub	238	(T)₉=0.983	delT=0.013, dupT=0.004, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	176	(T)₉=1.000	delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	88	(T)₉=1.00	delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	70	(T)₉=1.00	delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	12	(T)₉=1.00	delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4680	(T)₉=0.6878	delT=0.3122
1000Genomes	African	Sub	1307	(T)₉=0.8363	delT=0.1637
1000Genomes	East Asian	Sub	997	(T)₉=0.337	delT=0.663
1000Genomes	South Asian	Sub	953	(T)₉=0.717	delT=0.283
1000Genomes	Europe	Sub	805	(T)₉=0.897	delT=0.103
1000Genomes	American	Sub	618	(T)₉=0.623	delT=0.377

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 12	NC_000012.12:g.48470691_48470692del
GRCh38.p14 chr 12	NC_000012.12:g.48470692del
GRCh38.p14 chr 12	NC_000012.12:g.48470692dup
GRCh38.p14 chr 12	NC_000012.12:g.48470691_48470692dup
GRCh37.p13 chr 12	NC_000012.11:g.48864474_48864475del
GRCh37.p13 chr 12	NC_000012.11:g.48864475del
GRCh37.p13 chr 12	NC_000012.11:g.48864475dup
GRCh37.p13 chr 12	NC_000012.11:g.48864474_48864475dup

Gene: C12orf54, chromosome 12 open reading frame 54 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C12orf54 transcript	NM_152319.4:c.	N/A	Genic Upstream Transcript Variant
C12orf54 transcript variant X2	XM_011537896.3:c.-20+1114… XM_011537896.3:c.-20+11142_-20+11143del	N/A	Intron Variant
C12orf54 transcript variant X1	XM_017018796.2:c.-93-3287… XM_017018796.2:c.-93-3287_-93-3286del	N/A	Intron Variant
C12orf54 transcript variant X3	XM_005268636.4:c.	N/A	Genic Upstream Transcript Variant

Gene: ANP32D, acidic nuclear phosphoprotein 32 family member D (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ANP32D transcript	NM_012404.3:c.	N/A	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	(T)₉=	delTT	delT	dupT	dupTT
GRCh38.p14 chr 12	NC_000012.12:g.48470684_48470692=	NC_000012.12:g.48470691_48470692del	NC_000012.12:g.48470692del	NC_000012.12:g.48470692dup	NC_000012.12:g.48470691_48470692dup
GRCh37.p13 chr 12	NC_000012.11:g.48864467_48864475=	NC_000012.11:g.48864474_48864475del	NC_000012.11:g.48864475del	NC_000012.11:g.48864475dup	NC_000012.11:g.48864474_48864475dup
C12orf54 transcript variant X2	XM_011537896.3:c.-20+11135=	XM_011537896.3:c.-20+11142_-20+11143del	XM_011537896.3:c.-20+11143del	XM_011537896.3:c.-20+11143dup	XM_011537896.3:c.-20+11142_-20+11143dup
C12orf54 transcript variant X1	XM_017018796.2:c.-93-3294=	XM_017018796.2:c.-93-3287_-93-3286del	XM_017018796.2:c.-93-3286del	XM_017018796.2:c.-93-3286dup	XM_017018796.2:c.-93-3287_-93-3286dup

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#.

54 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40123846	Mar 13, 2006 (126)
2	BUSHMAN	ss193276840	Jul 04, 2010 (132)
3	GMI	ss287891095	Dec 06, 2013 (138)
4	GMI	ss289127281	May 04, 2012 (137)
5	1000GENOMES	ss327436591	May 09, 2011 (137)
6	1000GENOMES	ss327530266	Jan 10, 2018 (151)
7	1000GENOMES	ss327972653	May 09, 2011 (137)
8	LUNTER	ss552213897	Apr 25, 2013 (138)
9	LUNTER	ss552492220	Apr 25, 2013 (138)
10	LUNTER	ss553485917	Apr 25, 2013 (138)
11	SSMP	ss664124512	Apr 01, 2015 (144)
12	1000GENOMES	ss1372136925	Aug 21, 2014 (142)
13	1000GENOMES	ss1372136928	Aug 21, 2014 (142)
14	EVA_UK10K_ALSPAC	ss1707458322	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1707458421	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1710558528	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1710558549	Apr 01, 2015 (144)
18	HAMMER_LAB	ss1807236327	Sep 08, 2015 (146)
19	SYSTEMSBIOZJU	ss2628075130	Jan 10, 2018 (151)
20	SWEGEN	ss3009651513	Jan 10, 2018 (151)
21	MCHAISSO	ss3064557784	Jan 10, 2018 (151)
22	BIOINF_KMB_FNS_UNIBA	ss3645251744	Oct 12, 2018 (152)
23	BIOINF_KMB_FNS_UNIBA	ss3645251745	Oct 12, 2018 (152)
24	EVA_DECODE	ss3693628449	Jul 13, 2019 (153)
25	EVA_DECODE	ss3693628450	Jul 13, 2019 (153)
26	EVA_DECODE	ss3693628451	Jul 13, 2019 (153)
27	ACPOP	ss3739003990	Jul 13, 2019 (153)
28	ACPOP	ss3739003991	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3815785490	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3815785491	Jul 13, 2019 (153)
31	EVA	ss3833112584	Apr 27, 2020 (154)
32	EVA	ss3840126747	Apr 27, 2020 (154)
33	EVA	ss3845613009	Apr 27, 2020 (154)
34	KOGIC	ss3971883418	Apr 27, 2020 (154)
35	KOGIC	ss3971883419	Apr 27, 2020 (154)
36	GNOMAD	ss4251414030	Apr 26, 2021 (155)
37	GNOMAD	ss4251414031	Apr 26, 2021 (155)
38	GNOMAD	ss4251414034	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5206215126	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5206215127	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5206215128	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5206215129	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5290732350	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5290732351	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5485494922	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5485494923	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5755970466	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5755970467	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5755970468	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5755970469	Oct 16, 2022 (156)
51	EVA	ss5837938224	Oct 16, 2022 (156)
52	EVA	ss5837938225	Oct 16, 2022 (156)
53	EVA	ss5850373245	Oct 16, 2022 (156)
54	EVA	ss5980737555	Oct 16, 2022 (156)
55	1000Genomes	NC_000012.11 - 48864467	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32028783 (NC_000012.11:48864466::T 780/3854) Row 32028784 (NC_000012.11:48864466:T: 268/3854)	-	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32028783 (NC_000012.11:48864466::T 780/3854) Row 32028784 (NC_000012.11:48864466:T: 268/3854)	-	Oct 12, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406694399 (NC_000012.12:48470683::T 18056/138846) Row 406694400 (NC_000012.12:48470683::TT 20/138886) Row 406694403 (NC_000012.12:48470683:T: 19389/138834)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406694399 (NC_000012.12:48470683::T 18056/138846) Row 406694400 (NC_000012.12:48470683::TT 20/138886) Row 406694403 (NC_000012.12:48470683:T: 19389/138834)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406694399 (NC_000012.12:48470683::T 18056/138846) Row 406694400 (NC_000012.12:48470683::TT 20/138886) Row 406694403 (NC_000012.12:48470683:T: 19389/138834)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406694399 (NC_000012.12:48470683::T 18056/138846) Row 406694400 (NC_000012.12:48470683::TT 20/138886) Row 406694403 (NC_000012.12:48470683:T: 19389/138834)...	-	Apr 26, 2021 (155)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 28261419 (NC_000012.12:48470683:T: 1198/1832) Row 28261420 (NC_000012.12:48470684::T 13/1832)	-	Apr 27, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 28261419 (NC_000012.12:48470683:T: 1198/1832) Row 28261420 (NC_000012.12:48470684::T 13/1832)	-	Apr 27, 2020 (154)
64	Northern Sweden Submission ignored due to conflicting rows: Row 12288855 (NC_000012.11:48864466::T 103/600) Row 12288856 (NC_000012.11:48864466:T: 63/600)	-	Jul 13, 2019 (153)
65	Northern Sweden Submission ignored due to conflicting rows: Row 12288855 (NC_000012.11:48864466::T 103/600) Row 12288856 (NC_000012.11:48864466:T: 63/600)	-	Jul 13, 2019 (153)
66	8.3KJPN Submission ignored due to conflicting rows: Row 64184433 (NC_000012.11:48864466:T: 9732/16760) Row 64184434 (NC_000012.11:48864466::T 1143/16760) Row 64184435 (NC_000012.11:48864466:TT: 1/16760)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 64184433 (NC_000012.11:48864466:T: 9732/16760) Row 64184434 (NC_000012.11:48864466::T 1143/16760) Row 64184435 (NC_000012.11:48864466:TT: 1/16760)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 64184433 (NC_000012.11:48864466:T: 9732/16760) Row 64184434 (NC_000012.11:48864466::T 1143/16760) Row 64184435 (NC_000012.11:48864466:TT: 1/16760)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 64184433 (NC_000012.11:48864466:T: 9732/16760) Row 64184434 (NC_000012.11:48864466::T 1143/16760) Row 64184435 (NC_000012.11:48864466:TT: 1/16760)...	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 89807570 (NC_000012.12:48470683:T: 16343/28258) Row 89807571 (NC_000012.12:48470683::T 1914/28258) Row 89807572 (NC_000012.12:48470683:TT: 1/28258)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 89807570 (NC_000012.12:48470683:T: 16343/28258) Row 89807571 (NC_000012.12:48470683::T 1914/28258) Row 89807572 (NC_000012.12:48470683:TT: 1/28258)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 89807570 (NC_000012.12:48470683:T: 16343/28258) Row 89807571 (NC_000012.12:48470683::T 1914/28258) Row 89807572 (NC_000012.12:48470683:TT: 1/28258)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 89807570 (NC_000012.12:48470683:T: 16343/28258) Row 89807571 (NC_000012.12:48470683::T 1914/28258) Row 89807572 (NC_000012.12:48470683:TT: 1/28258)...	-	Oct 16, 2022 (156)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32028783 (NC_000012.11:48864466::T 756/3708) Row 32028784 (NC_000012.11:48864466:T: 229/3708)	-	Oct 12, 2018 (152)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32028783 (NC_000012.11:48864466::T 756/3708) Row 32028784 (NC_000012.11:48864466:T: 229/3708)	-	Oct 12, 2018 (152)
76	ALFA	NC_000012.12 - 48470684	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)
rs137994782	May 11, 2012 (137)
rs146249064	May 04, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5206215128	NC_000012.11:48864466:TT:	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTT	(self)
ss4251414034, ss5755970468	NC_000012.12:48470683:TT:	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTT	(self)
ss289127281, ss327436591, ss327972653, ss552492220, ss553485917	NC_000012.10:47150733:T:	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTT	(self)
57677008, ss664124512, ss1372136925, ss1707458322, ss1707458421, ss1807236327, ss2628075130, ss3009651513, ss3739003991, ss5206215126, ss5837938225, ss5980737555	NC_000012.11:48864466:T:	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTT	(self)
ss3064557784, ss3645251745, ss3693628449, ss3815785490, ss3971883418, ss5290732350, ss5485494923, ss5755970466, ss5850373245	NC_000012.12:48470683:T:	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTT	(self)
15852582059	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTT	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTT	(self)
ss40123846	NT_029419.12:11007772:T:	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTT	(self)
ss193276840	NT_029419.13:11235431:T:	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTT	(self)
ss327530266, ss552213897	NC_000012.10:47150733::T	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	(self)
ss3739003990, ss3833112584, ss3840126747, ss5206215127, ss5837938224	NC_000012.11:48864466::T	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	(self)
ss1372136928, ss1710558528, ss1710558549	NC_000012.11:48864467::T	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	(self)
ss3645251744, ss3845613009, ss4251414030, ss5290732351, ss5485494922, ss5755970467	NC_000012.12:48470683::T	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	(self)
15852582059	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	(self)
ss3693628450, ss3815785491, ss3971883419	NC_000012.12:48470684::T	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	(self)
ss287891095	NT_029419.12:11007781::T	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTT	(self)
ss5206215129	NC_000012.11:48864466::TT	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTTT	(self)
ss4251414031, ss5755970469	NC_000012.12:48470683::TT	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTTT	(self)
15852582059	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTTT	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTTT	(self)
ss3693628451	NC_000012.12:48470684::TT	NC_000012.12:48470683:TTTTTTTTT:TT… NC_000012.12:48470683:TTTTTTTTT:TTTTTTTTTTT	(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 rs34351264

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

rs34351264