Name: rs35434258
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.

rs35434258

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:183147916-183147928 (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 / dup(…
delTT / delT / dupT / dupTT / dup(T)₇
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.220205 (58286/264690, TOPMED)
delT=0.08268 (904/10934, ALFA)
delT=0.2226 (1003/4505, 1000G) (+ 2 more)
delT=0.1684 (649/3854, ALSPAC)
delT=0.1923 (713/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NUP35 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	10934	TTTTTTTTTTTTT=0.90113	TTTTTTTTTTT=0.00009, TTTTTTTTTTTT=0.08268, TTTTTTTTTTTTTT=0.01610, TTTTTTTTTTTTTTT=0.00000	0.853391	0.019649	0.12696	32
European	Sub	8880	TTTTTTTTTTTTT=0.8783	TTTTTTTTTTT=0.0001, TTTTTTTTTTTT=0.1018, TTTTTTTTTTTTTT=0.0198, TTTTTTTTTTTTTTT=0.0000	0.818097	0.024379	0.157525	32
African	Sub	1172	TTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	34	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1138	TTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	58	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	86	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	414	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	50	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	274	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=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
TopMed	Global	Study-wide	264690	(T)₁₃=0.779795	delT=0.220205
Allele Frequency Aggregator	Total	Global	10934	(T)₁₃=0.90113	delTT=0.00009, delT=0.08268, dupT=0.01610, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	8880	(T)₁₃=0.8783	delTT=0.0001, delT=0.1018, dupT=0.0198, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1172	(T)₁₃=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	414	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	274	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	86	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	58	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4505	(T)₁₃=0.7774	delT=0.2226
1000Genomes	African	Sub	1255	(T)₁₃=0.6406	delT=0.3594
1000Genomes	Europe	Sub	942	(T)₁₃=0.811	delT=0.189
1000Genomes	East Asian	Sub	882	(T)₁₃=0.859	delT=0.141
1000Genomes	South Asian	Sub	801	(T)₁₃=0.811	delT=0.189
1000Genomes	American	Sub	625	(T)₁₃=0.842	delT=0.158
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₃=0.8316	delT=0.1684
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₃=0.8077	delT=0.1923

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 2	NC_000002.12:g.183147927_183147928del
GRCh38.p14 chr 2	NC_000002.12:g.183147928del
GRCh38.p14 chr 2	NC_000002.12:g.183147928dup
GRCh38.p14 chr 2	NC_000002.12:g.183147927_183147928dup
GRCh38.p14 chr 2	NC_000002.12:g.183147922_183147928dup
GRCh37.p13 chr 2	NC_000002.11:g.184012655_184012656del
GRCh37.p13 chr 2	NC_000002.11:g.184012656del
GRCh37.p13 chr 2	NC_000002.11:g.184012656dup
GRCh37.p13 chr 2	NC_000002.11:g.184012655_184012656dup
GRCh37.p13 chr 2	NC_000002.11:g.184012650_184012656dup

Gene: NUP35, nucleoporin 35 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NUP35 transcript variant 3	NM_001287584.2:c.347-3581… NM_001287584.2:c.347-3581_347-3580del	N/A	Intron Variant
NUP35 transcript variant 4	NM_001287585.2:c.44-3581_… NM_001287585.2:c.44-3581_44-3580del	N/A	Intron Variant
NUP35 transcript variant 1	NM_138285.5:c.398-3581_39… NM_138285.5:c.398-3581_398-3580del	N/A	Intron Variant
NUP35 transcript variant 2	NR_109856.2:n.	N/A	Intron Variant
NUP35 transcript variant X2	XM_006712254.4:c.347-3581… XM_006712254.4:c.347-3581_347-3580del	N/A	Intron Variant
NUP35 transcript variant X5	XM_011510576.4:c.347-3581… XM_011510576.4:c.347-3581_347-3580del	N/A	Intron Variant
NUP35 transcript variant X3	XM_011510577.3:c.347-3581… XM_011510577.3:c.347-3581_347-3580del	N/A	Intron Variant
NUP35 transcript variant X1	XM_017003308.1:c.407-3581… XM_017003308.1:c.407-3581_407-3580del	N/A	Intron Variant
NUP35 transcript variant X4	XM_047443270.1:c.347-3581… XM_047443270.1:c.347-3581_347-3580del	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=	delTT	delT	dupT	dupTT	dup(T)₇
GRCh38.p14 chr 2	NC_000002.12:g.183147916_183147928=	NC_000002.12:g.183147927_183147928del	NC_000002.12:g.183147928del	NC_000002.12:g.183147928dup	NC_000002.12:g.183147927_183147928dup	NC_000002.12:g.183147922_183147928dup
GRCh37.p13 chr 2	NC_000002.11:g.184012644_184012656=	NC_000002.11:g.184012655_184012656del	NC_000002.11:g.184012656del	NC_000002.11:g.184012656dup	NC_000002.11:g.184012655_184012656dup	NC_000002.11:g.184012650_184012656dup
NUP35 transcript variant 3	NM_001287584.2:c.347-3592=	NM_001287584.2:c.347-3581_347-3580del	NM_001287584.2:c.347-3580del	NM_001287584.2:c.347-3580dup	NM_001287584.2:c.347-3581_347-3580dup	NM_001287584.2:c.347-3586_347-3580dup
NUP35 transcript variant 4	NM_001287585.2:c.44-3592=	NM_001287585.2:c.44-3581_44-3580del	NM_001287585.2:c.44-3580del	NM_001287585.2:c.44-3580dup	NM_001287585.2:c.44-3581_44-3580dup	NM_001287585.2:c.44-3586_44-3580dup
NUP35 transcript	NM_138285.3:c.398-3592=	NM_138285.3:c.398-3581_398-3580del	NM_138285.3:c.398-3580del	NM_138285.3:c.398-3580dup	NM_138285.3:c.398-3581_398-3580dup	NM_138285.3:c.398-3586_398-3580dup
NUP35 transcript variant 1	NM_138285.5:c.398-3592=	NM_138285.5:c.398-3581_398-3580del	NM_138285.5:c.398-3580del	NM_138285.5:c.398-3580dup	NM_138285.5:c.398-3581_398-3580dup	NM_138285.5:c.398-3586_398-3580dup
NUP35 transcript variant X1	XM_005246284.1:c.407-3592=	XM_005246284.1:c.407-3581_407-3580del	XM_005246284.1:c.407-3580del	XM_005246284.1:c.407-3580dup	XM_005246284.1:c.407-3581_407-3580dup	XM_005246284.1:c.407-3586_407-3580dup
NUP35 transcript variant X2	XM_005246285.1:c.347-3592=	XM_005246285.1:c.347-3581_347-3580del	XM_005246285.1:c.347-3580del	XM_005246285.1:c.347-3580dup	XM_005246285.1:c.347-3581_347-3580dup	XM_005246285.1:c.347-3586_347-3580dup
NUP35 transcript variant X3	XM_005246286.1:c.44-3592=	XM_005246286.1:c.44-3581_44-3580del	XM_005246286.1:c.44-3580del	XM_005246286.1:c.44-3580dup	XM_005246286.1:c.44-3581_44-3580dup	XM_005246286.1:c.44-3586_44-3580dup
NUP35 transcript variant X2	XM_006712254.4:c.347-3592=	XM_006712254.4:c.347-3581_347-3580del	XM_006712254.4:c.347-3580del	XM_006712254.4:c.347-3580dup	XM_006712254.4:c.347-3581_347-3580dup	XM_006712254.4:c.347-3586_347-3580dup
NUP35 transcript variant X5	XM_011510576.4:c.347-3592=	XM_011510576.4:c.347-3581_347-3580del	XM_011510576.4:c.347-3580del	XM_011510576.4:c.347-3580dup	XM_011510576.4:c.347-3581_347-3580dup	XM_011510576.4:c.347-3586_347-3580dup
NUP35 transcript variant X3	XM_011510577.3:c.347-3592=	XM_011510577.3:c.347-3581_347-3580del	XM_011510577.3:c.347-3580del	XM_011510577.3:c.347-3580dup	XM_011510577.3:c.347-3581_347-3580dup	XM_011510577.3:c.347-3586_347-3580dup
NUP35 transcript variant X1	XM_017003308.1:c.407-3592=	XM_017003308.1:c.407-3581_407-3580del	XM_017003308.1:c.407-3580del	XM_017003308.1:c.407-3580dup	XM_017003308.1:c.407-3581_407-3580dup	XM_017003308.1:c.407-3586_407-3580dup
NUP35 transcript variant X4	XM_047443270.1:c.347-3592=	XM_047443270.1:c.347-3581_347-3580del	XM_047443270.1:c.347-3580del	XM_047443270.1:c.347-3580dup	XM_047443270.1:c.347-3581_347-3580dup	XM_047443270.1:c.347-3586_347-3580dup

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#.

50 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41681688	Dec 03, 2013 (144)
2	HUMANGENOME_JCVI	ss96733908	Feb 13, 2009 (137)
3	GMI	ss288263599	May 04, 2012 (137)
4	GMI	ss288263601	May 04, 2012 (137)
5	PJP	ss295017554	May 09, 2011 (134)
6	SSMP	ss663265434	Apr 01, 2015 (144)
7	1000GENOMES	ss1369287276	Aug 21, 2014 (142)
8	1000GENOMES	ss1369287279	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1703314753	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1703314767	Apr 01, 2015 (144)
11	JJLAB	ss2030464432	Sep 14, 2016 (149)
12	SYSTEMSBIOZJU	ss2625017444	Nov 08, 2017 (151)
13	SWEGEN	ss2990997192	Nov 17, 2017 (151)
14	MCHAISSO	ss3063969966	Nov 08, 2017 (151)
15	MCHAISSO	ss3065782649	Nov 08, 2017 (151)
16	BEROUKHIMLAB	ss3644108660	Oct 11, 2018 (152)
17	URBANLAB	ss3647225177	Oct 11, 2018 (152)
18	EVA_DECODE	ss3705582383	Jul 13, 2019 (153)
19	EVA_DECODE	ss3705582384	Jul 13, 2019 (153)
20	EVA_DECODE	ss3705582385	Jul 13, 2019 (153)
21	EVA_DECODE	ss3705582386	Jul 13, 2019 (153)
22	ACPOP	ss3729179363	Jul 13, 2019 (153)
23	ACPOP	ss3729179364	Jul 13, 2019 (153)
24	PACBIO	ss3784089220	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3802175488	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3802175489	Jul 13, 2019 (153)
27	EVA	ss3827394648	Apr 25, 2020 (154)
28	EVA	ss3837116225	Apr 25, 2020 (154)
29	EVA	ss3842536649	Apr 25, 2020 (154)
30	KOGIC	ss3949653282	Apr 25, 2020 (154)
31	KOGIC	ss3949653283	Apr 25, 2020 (154)
32	GNOMAD	ss4057019181	Apr 26, 2021 (155)
33	GNOMAD	ss4057019182	Apr 26, 2021 (155)
34	GNOMAD	ss4057019183	Apr 26, 2021 (155)
35	TOPMED	ss4536539443	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5155476231	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5155476232	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5251244235	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5251244236	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5251244237	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5450940704	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5450940705	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5450940706	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5686062863	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5686062864	Oct 12, 2022 (156)
46	EVA	ss5821289366	Oct 12, 2022 (156)
47	EVA	ss5821289367	Oct 12, 2022 (156)
48	EVA	ss5852865562	Oct 12, 2022 (156)
49	EVA	ss5933800841	Oct 12, 2022 (156)
50	EVA	ss5956747919	Oct 12, 2022 (156)
51	1000Genomes	NC_000002.11 - 184012644	Oct 11, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 184012644	Oct 11, 2018 (152)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84193265 (NC_000002.12:183147915::T 7070/134030) Row 84193266 (NC_000002.12:183147915::TT 8/134122) Row 84193267 (NC_000002.12:183147915:T: 30006/133912)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84193265 (NC_000002.12:183147915::T 7070/134030) Row 84193266 (NC_000002.12:183147915::TT 8/134122) Row 84193267 (NC_000002.12:183147915:T: 30006/133912)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84193265 (NC_000002.12:183147915::T 7070/134030) Row 84193266 (NC_000002.12:183147915::TT 8/134122) Row 84193267 (NC_000002.12:183147915:T: 30006/133912)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84193265 (NC_000002.12:183147915::T 7070/134030) Row 84193266 (NC_000002.12:183147915::TT 8/134122) Row 84193267 (NC_000002.12:183147915:T: 30006/133912)...	-	Apr 26, 2021 (155)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 6031283 (NC_000002.12:183147915:T: 272/1832) Row 6031284 (NC_000002.12:183147916::T 208/1832)	-	Apr 25, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 6031283 (NC_000002.12:183147915:T: 272/1832) Row 6031284 (NC_000002.12:183147916::T 208/1832)	-	Apr 25, 2020 (154)
59	Northern Sweden Submission ignored due to conflicting rows: Row 2464228 (NC_000002.11:184012643:T: 103/600) Row 2464229 (NC_000002.11:184012643::T 18/600)	-	Jul 13, 2019 (153)
60	Northern Sweden Submission ignored due to conflicting rows: Row 2464228 (NC_000002.11:184012643:T: 103/600) Row 2464229 (NC_000002.11:184012643::T 18/600)	-	Jul 13, 2019 (153)
61	8.3KJPN Submission ignored due to conflicting rows: Row 13445538 (NC_000002.11:184012643::T 1374/16760) Row 13445539 (NC_000002.11:184012643:T: 2386/16760)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 13445538 (NC_000002.11:184012643::T 1374/16760) Row 13445539 (NC_000002.11:184012643:T: 2386/16760)	-	Apr 26, 2021 (155)
63	14KJPN Submission ignored due to conflicting rows: Row 19899967 (NC_000002.12:183147915:T: 4039/28256) Row 19899968 (NC_000002.12:183147915::T 2205/28256)	-	Oct 12, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 19899967 (NC_000002.12:183147915:T: 4039/28256) Row 19899968 (NC_000002.12:183147915::T 2205/28256)	-	Oct 12, 2022 (156)
65	TopMed	NC_000002.12 - 183147916	Apr 26, 2021 (155)
66	UK 10K study - Twins	NC_000002.11 - 184012644	Oct 11, 2018 (152)
67	ALFA	NC_000002.12 - 183147916	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)
rs71407013	May 11, 2012 (137)
rs397870696	Jul 01, 2015 (144)
rs372655134	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss2990997192	NC_000002.11:184012643:TT:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3705582383, ss4057019183, ss5251244237, ss5450940706	NC_000002.12:183147915:TT:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
8449029899	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss288263599	NC_000002.10:183720888:T:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss295017554	NC_000002.10:183720900:T:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
11814589, 6528424, 6528424, ss1369287276, ss1703314753, ss1703314767, ss2030464432, ss3644108660, ss3729179363, ss3784089220, ss3827394648, ss3837116225, ss5155476232, ss5821289366, ss5956747919	NC_000002.11:184012643:T:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
340362322, ss3647225177, ss3802175489, ss3842536649, ss3949653282, ss4536539443, ss5251244236, ss5450940704, ss5686062863, ss5933800841	NC_000002.12:183147915:T:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
8449029899	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3705582384	NC_000002.12:183147916:T:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss96733908	NT_005403.17:34222061:T:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss41681688	NT_005403.17:34222073:T:	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss288263601	NC_000002.10:183720901::T	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss663265434, ss2625017444, ss3729179364, ss5155476231	NC_000002.11:184012643::T	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1369287279	NC_000002.11:184012644::T	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3063969966, ss3065782649, ss4057019181, ss5251244235, ss5450940705, ss5686062864, ss5852865562	NC_000002.12:183147915::T	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
8449029899	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3802175488, ss3949653283	NC_000002.12:183147916::T	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3705582385	NC_000002.12:183147917::T	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4057019182	NC_000002.12:183147915::TT	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
8449029899	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3705582386	NC_000002.12:183147917::TT	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5821289367	NC_000002.11:184012643::TTTTTTT	NC_000002.12:183147915:TTTTTTTTTTT… NC_000002.12:183147915:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs35434258

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

rs35434258