Name: rs34499342
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.

rs34499342

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:111648206-111648218 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT
Variation Type: Indel Insertion and Deletion
Frequency: delTTT=0.0000 (0/2730, ALFA)
delTT=0.0000 (0/2730, ALFA)
delT=0.0000 (0/2730, ALFA) (+ 1 more)
dupT=0.0000 (0/2730, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RAP1A : 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	2730	TTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	1828	TTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	468	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	16	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	452	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	28	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	24	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0	1.0	N/A
Latin American 1	Sub	48	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	200	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	20	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	138	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	2730	(T)₁₃=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	European	Sub	1828	(T)₁₃=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	African	Sub	468	(T)₁₃=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	200	(T)₁₃=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Other	Sub	138	(T)₁₃=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	48	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	Asian	Sub	28	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=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 1	NC_000001.11:g.111648215_111648218del
GRCh38.p14 chr 1	NC_000001.11:g.111648216_111648218del
GRCh38.p14 chr 1	NC_000001.11:g.111648217_111648218del
GRCh38.p14 chr 1	NC_000001.11:g.111648218del
GRCh38.p14 chr 1	NC_000001.11:g.111648218dup
GRCh37.p13 chr 1	NC_000001.10:g.112190837_112190840del
GRCh37.p13 chr 1	NC_000001.10:g.112190838_112190840del
GRCh37.p13 chr 1	NC_000001.10:g.112190839_112190840del
GRCh37.p13 chr 1	NC_000001.10:g.112190840del
GRCh37.p13 chr 1	NC_000001.10:g.112190840dup
KRT18P57 pseudogene	NG_022732.2:g.1489_1492del
KRT18P57 pseudogene	NG_022732.2:g.1490_1492del
KRT18P57 pseudogene	NG_022732.2:g.1491_1492del
KRT18P57 pseudogene	NG_022732.2:g.1492del
KRT18P57 pseudogene	NG_022732.2:g.1492dup

Gene: RAP1A, RAP1A, member of RAS oncogene family (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RAP1A transcript variant 1	NM_001010935.3:c.-28+2065… NM_001010935.3:c.-28+20652_-28+20655del	N/A	Intron Variant
RAP1A transcript variant 3	NM_001291896.3:c.-28+2786… NM_001291896.3:c.-28+27868_-28+27871del	N/A	Intron Variant
RAP1A transcript variant 4	NM_001370216.2:c.-27-4311… NM_001370216.2:c.-27-43119_-27-43116del	N/A	Intron Variant
RAP1A transcript variant 5	NM_001370217.2:c.-107-165… NM_001370217.2:c.-107-16577_-107-16574del	N/A	Intron Variant
RAP1A transcript variant 6	NM_001394066.1:c.-107-165… NM_001394066.1:c.-107-16577_-107-16574del	N/A	Intron Variant
RAP1A transcript variant 2	NM_002884.4:c.-28+28281_-… NM_002884.4:c.-28+28281_-28+28284del	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)₁₃=	del(T)₄	delTTT	delTT	delT	dupT
GRCh38.p14 chr 1	NC_000001.11:g.111648206_111648218=	NC_000001.11:g.111648215_111648218del	NC_000001.11:g.111648216_111648218del	NC_000001.11:g.111648217_111648218del	NC_000001.11:g.111648218del	NC_000001.11:g.111648218dup
GRCh37.p13 chr 1	NC_000001.10:g.112190828_112190840=	NC_000001.10:g.112190837_112190840del	NC_000001.10:g.112190838_112190840del	NC_000001.10:g.112190839_112190840del	NC_000001.10:g.112190840del	NC_000001.10:g.112190840dup
KRT18P57 pseudogene	NG_022732.2:g.1480_1492=	NG_022732.2:g.1489_1492del	NG_022732.2:g.1490_1492del	NG_022732.2:g.1491_1492del	NG_022732.2:g.1492del	NG_022732.2:g.1492dup
RAP1A transcript variant 1	NM_001010935.1:c.-28+20643=	NM_001010935.1:c.-28+20652_-28+20655del	NM_001010935.1:c.-28+20653_-28+20655del	NM_001010935.1:c.-28+20654_-28+20655del	NM_001010935.1:c.-28+20655del	NM_001010935.1:c.-28+20655dup
RAP1A transcript variant 1	NM_001010935.3:c.-28+20643=	NM_001010935.3:c.-28+20652_-28+20655del	NM_001010935.3:c.-28+20653_-28+20655del	NM_001010935.3:c.-28+20654_-28+20655del	NM_001010935.3:c.-28+20655del	NM_001010935.3:c.-28+20655dup
RAP1A transcript variant 3	NM_001291896.3:c.-28+27859=	NM_001291896.3:c.-28+27868_-28+27871del	NM_001291896.3:c.-28+27869_-28+27871del	NM_001291896.3:c.-28+27870_-28+27871del	NM_001291896.3:c.-28+27871del	NM_001291896.3:c.-28+27871dup
RAP1A transcript variant 4	NM_001370216.2:c.-27-43128=	NM_001370216.2:c.-27-43119_-27-43116del	NM_001370216.2:c.-27-43118_-27-43116del	NM_001370216.2:c.-27-43117_-27-43116del	NM_001370216.2:c.-27-43116del	NM_001370216.2:c.-27-43116dup
RAP1A transcript variant 5	NM_001370217.2:c.-107-16586=	NM_001370217.2:c.-107-16577_-107-16574del	NM_001370217.2:c.-107-16576_-107-16574del	NM_001370217.2:c.-107-16575_-107-16574del	NM_001370217.2:c.-107-16574del	NM_001370217.2:c.-107-16574dup
RAP1A transcript variant 6	NM_001394066.1:c.-107-16586=	NM_001394066.1:c.-107-16577_-107-16574del	NM_001394066.1:c.-107-16576_-107-16574del	NM_001394066.1:c.-107-16575_-107-16574del	NM_001394066.1:c.-107-16574del	NM_001394066.1:c.-107-16574dup
RAP1A transcript variant 2	NM_002884.2:c.-28+28272=	NM_002884.2:c.-28+28281_-28+28284del	NM_002884.2:c.-28+28282_-28+28284del	NM_002884.2:c.-28+28283_-28+28284del	NM_002884.2:c.-28+28284del	NM_002884.2:c.-28+28284dup
RAP1A transcript variant 2	NM_002884.4:c.-28+28272=	NM_002884.4:c.-28+28281_-28+28284del	NM_002884.4:c.-28+28282_-28+28284del	NM_002884.4:c.-28+28283_-28+28284del	NM_002884.4:c.-28+28284del	NM_002884.4:c.-28+28284dup

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, 14 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41287652	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss95240437	Mar 15, 2016 (147)
3	BUSHMAN	ss193121859	Jul 04, 2010 (137)
4	GMI	ss287679397	May 09, 2011 (137)
5	GMI	ss288027288	May 04, 2012 (137)
6	PJP	ss294598536	Sep 08, 2015 (146)
7	SSMP	ss663110195	Apr 01, 2015 (144)
8	BIOINF_KMB_FNS_UNIBA	ss3645066114	Oct 11, 2018 (152)
9	URBANLAB	ss3646753044	Oct 11, 2018 (152)
10	EVA_DECODE	ss3687535857	Jul 12, 2019 (153)
11	EVA_DECODE	ss3687535858	Jul 12, 2019 (153)
12	EVA_DECODE	ss3687535859	Jul 12, 2019 (153)
13	EVA_DECODE	ss3687535860	Jul 12, 2019 (153)
14	ACPOP	ss3727391491	Jul 12, 2019 (153)
15	ACPOP	ss3727391493	Jul 12, 2019 (153)
16	EVA	ss3826371281	Apr 25, 2020 (154)
17	GNOMAD	ss4000485538	Apr 25, 2021 (155)
18	GNOMAD	ss4000485541	Apr 25, 2021 (155)
19	GNOMAD	ss4000485542	Apr 25, 2021 (155)
20	GNOMAD	ss4000485543	Apr 25, 2021 (155)
21	GNOMAD	ss4000485544	Apr 25, 2021 (155)
22	TOMMO_GENOMICS	ss5145692263	Apr 25, 2021 (155)
23	TOMMO_GENOMICS	ss5145692264	Apr 25, 2021 (155)
24	TOMMO_GENOMICS	ss5145692265	Apr 25, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5243618366	Oct 12, 2022 (156)
26	HUGCELL_USP	ss5444541447	Oct 12, 2022 (156)
27	HUGCELL_USP	ss5444541449	Oct 12, 2022 (156)
28	TOMMO_GENOMICS	ss5670963138	Oct 12, 2022 (156)
29	TOMMO_GENOMICS	ss5670963141	Oct 12, 2022 (156)
30	TOMMO_GENOMICS	ss5670963142	Oct 12, 2022 (156)
31	EVA	ss5832487959	Oct 12, 2022 (156)
32	EVA	ss5832487960	Oct 12, 2022 (156)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22768677 (NC_000001.11:111648205::T 50/121576) Row 22768680 (NC_000001.11:111648205:T: 48098/121376) Row 22768681 (NC_000001.11:111648205:TT: 6344/121510)...	-	Apr 25, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22768677 (NC_000001.11:111648205::T 50/121576) Row 22768680 (NC_000001.11:111648205:T: 48098/121376) Row 22768681 (NC_000001.11:111648205:TT: 6344/121510)...	-	Apr 25, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22768677 (NC_000001.11:111648205::T 50/121576) Row 22768680 (NC_000001.11:111648205:T: 48098/121376) Row 22768681 (NC_000001.11:111648205:TT: 6344/121510)...	-	Apr 25, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22768677 (NC_000001.11:111648205::T 50/121576) Row 22768680 (NC_000001.11:111648205:T: 48098/121376) Row 22768681 (NC_000001.11:111648205:TT: 6344/121510)...	-	Apr 25, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22768677 (NC_000001.11:111648205::T 50/121576) Row 22768680 (NC_000001.11:111648205:T: 48098/121376) Row 22768681 (NC_000001.11:111648205:TT: 6344/121510)...	-	Apr 25, 2021 (155)
38	Northern Sweden Submission ignored due to conflicting rows: Row 676356 (NC_000001.10:112190827:T: 185/572) Row 676358 (NC_000001.10:112190827:TT: 36/572)	-	Jul 12, 2019 (153)
39	Northern Sweden Submission ignored due to conflicting rows: Row 676356 (NC_000001.10:112190827:T: 185/572) Row 676358 (NC_000001.10:112190827:TT: 36/572)	-	Jul 12, 2019 (153)
40	8.3KJPN Submission ignored due to conflicting rows: Row 3661570 (NC_000001.10:112190827:T: 3181/16722) Row 3661571 (NC_000001.10:112190827:TT: 73/16722) Row 3661572 (NC_000001.10:112190827::T 20/16722)	-	Apr 25, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 3661570 (NC_000001.10:112190827:T: 3181/16722) Row 3661571 (NC_000001.10:112190827:TT: 73/16722) Row 3661572 (NC_000001.10:112190827::T 20/16722)	-	Apr 25, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 3661570 (NC_000001.10:112190827:T: 3181/16722) Row 3661571 (NC_000001.10:112190827:TT: 73/16722) Row 3661572 (NC_000001.10:112190827::T 20/16722)	-	Apr 25, 2021 (155)
43	14KJPN Submission ignored due to conflicting rows: Row 4800242 (NC_000001.11:111648205:T: 5743/27136) Row 4800245 (NC_000001.11:111648205:TT: 125/27136) Row 4800246 (NC_000001.11:111648205::T 32/27136)	-	Oct 12, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 4800242 (NC_000001.11:111648205:T: 5743/27136) Row 4800245 (NC_000001.11:111648205:TT: 125/27136) Row 4800246 (NC_000001.11:111648205::T 32/27136)	-	Oct 12, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 4800242 (NC_000001.11:111648205:T: 5743/27136) Row 4800245 (NC_000001.11:111648205:TT: 125/27136) Row 4800246 (NC_000001.11:111648205::T 32/27136)	-	Oct 12, 2022 (156)
46	ALFA	NC_000001.11 - 111648206	Apr 25, 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)
rs72275030	Oct 12, 2011 (135)
rs61066333	May 26, 2008 (130)
rs145511344	May 13, 2013 (138)
rs113619677	May 11, 2012 (137)
rs374376142	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4000485544	NC_000001.11:111648205:TTTT:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3687535857, ss4000485543	NC_000001.11:111648205:TTT:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
5309506421	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTT	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss294598536	NC_000001.9:111992361:TT:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3727391493, ss5145692264, ss5832487960	NC_000001.10:112190827:TT:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3646753044, ss4000485542, ss5444541449, ss5670963141	NC_000001.11:111648205:TT:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
5309506421	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3687535858	NC_000001.11:111648206:TT:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss95240437	NT_032977.9:82162756:TT:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss288027288	NC_000001.9:111992350:T:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss663110195, ss3727391491, ss3826371281, ss5145692263, ss5832487959	NC_000001.10:112190827:T:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3645066114, ss4000485541, ss5243618366, ss5444541447, ss5670963138	NC_000001.11:111648205:T:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5309506421	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3687535859	NC_000001.11:111648207:T:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss287679397	NT_032977.9:82162745:T:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss41287652	NT_032977.9:82162746:T:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss193121859	NT_032977.10:111062217:T:	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5145692265	NC_000001.10:112190827::T	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4000485538, ss5670963142	NC_000001.11:111648205::T	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5309506421	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3687535860	NC_000001.11:111648208::T	NC_000001.11:111648205:TTTTTTTTTTT… NC_000001.11:111648205:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(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 rs34499342

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

rs34499342