Name: rs34331888
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.

rs34331888

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:183128600-183128614 (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(A)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.1569 (1208/7698, ALFA)
delA=0.4093 (2050/5008, 1000G)
delAA=0.1674 (645/3854, ALSPAC)

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	7698	AAAAAAAAAAAAAAA=0.7537	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0891, AAAAAAAAAAAAAA=0.1569, AAAAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAAAAAAA=0.0000	0.736012	0.057805	0.206182	32
European	Sub	6788	AAAAAAAAAAAAAAA=0.7211	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.1008, AAAAAAAAAAAAAA=0.1778, AAAAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAAAAAAA=0.0000	0.693386	0.067218	0.239396	32
African	Sub	288	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	282	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	56	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	58	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	312	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	32	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	164	AAAAAAAAAAAAAAA=0.982	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.012, AAAAAAAAAAAAAA=0.006, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	0.9875	0.0	0.0125	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	7698	(A)₁₅=0.7537	delAAA=0.0000, delAA=0.0891, delA=0.1569, dupA=0.0003, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	6788	(A)₁₅=0.7211	delAAA=0.0000, delAA=0.1008, delA=0.1778, dupA=0.0003, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	312	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	African	Sub	288	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	164	(A)₁₅=0.982	delAAA=0.000, delAA=0.012, delA=0.006, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	58	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	56	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.5907	delA=0.4093
1000Genomes	African	Sub	1322	(A)₁₅=0.3979	delA=0.6021
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.7222	delA=0.2778
1000Genomes	Europe	Sub	1006	(A)₁₅=0.6431	delA=0.3569
1000Genomes	South Asian	Sub	978	(A)₁₅=0.611	delA=0.389
1000Genomes	American	Sub	694	(A)₁₅=0.661	delA=0.339
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₅=0.8326	delAA=0.1674

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.183128611_183128614del
GRCh38.p14 chr 2	NC_000002.12:g.183128612_183128614del
GRCh38.p14 chr 2	NC_000002.12:g.183128613_183128614del
GRCh38.p14 chr 2	NC_000002.12:g.183128614del
GRCh38.p14 chr 2	NC_000002.12:g.183128614dup
GRCh38.p14 chr 2	NC_000002.12:g.183128613_183128614dup
GRCh37.p13 chr 2	NC_000002.11:g.183993339_183993342del
GRCh37.p13 chr 2	NC_000002.11:g.183993340_183993342del
GRCh37.p13 chr 2	NC_000002.11:g.183993341_183993342del
GRCh37.p13 chr 2	NC_000002.11:g.183993342del
GRCh37.p13 chr 2	NC_000002.11:g.183993342dup
GRCh37.p13 chr 2	NC_000002.11:g.183993341_183993342dup

Gene: NUP35, nucleoporin 35 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NUP35 transcript variant 3	NM_001287584.2:c.160+154_… NM_001287584.2:c.160+154_160+157del	N/A	Intron Variant
NUP35 transcript variant 4	NM_001287585.2:c.-267+154… NM_001287585.2:c.-267+154_-267+157del	N/A	Intron Variant
NUP35 transcript variant 1	NM_138285.5:c.211+154_211… NM_138285.5:c.211+154_211+157del	N/A	Intron Variant
NUP35 transcript variant 2	NR_109856.2:n.	N/A	Intron Variant
NUP35 transcript variant X2	XM_006712254.4:c.160+154_… XM_006712254.4:c.160+154_160+157del	N/A	Intron Variant
NUP35 transcript variant X5	XM_011510576.4:c.160+154_… XM_011510576.4:c.160+154_160+157del	N/A	Intron Variant
NUP35 transcript variant X3	XM_011510577.3:c.160+154_… XM_011510577.3:c.160+154_160+157del	N/A	Intron Variant
NUP35 transcript variant X1	XM_017003308.1:c.220+154_… XM_017003308.1:c.220+154_220+157del	N/A	Intron Variant
NUP35 transcript variant X4	XM_047443270.1:c.160+154_… XM_047443270.1:c.160+154_160+157del	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	(A)₁₅=	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 2	NC_000002.12:g.183128600_183128614=	NC_000002.12:g.183128611_183128614del	NC_000002.12:g.183128612_183128614del	NC_000002.12:g.183128613_183128614del	NC_000002.12:g.183128614del	NC_000002.12:g.183128614dup	NC_000002.12:g.183128613_183128614dup
GRCh37.p13 chr 2	NC_000002.11:g.183993328_183993342=	NC_000002.11:g.183993339_183993342del	NC_000002.11:g.183993340_183993342del	NC_000002.11:g.183993341_183993342del	NC_000002.11:g.183993342del	NC_000002.11:g.183993342dup	NC_000002.11:g.183993341_183993342dup
NUP35 transcript variant 3	NM_001287584.2:c.160+143=	NM_001287584.2:c.160+154_160+157del	NM_001287584.2:c.160+155_160+157del	NM_001287584.2:c.160+156_160+157del	NM_001287584.2:c.160+157del	NM_001287584.2:c.160+157dup	NM_001287584.2:c.160+156_160+157dup
NUP35 transcript variant 4	NM_001287585.2:c.-267+143=	NM_001287585.2:c.-267+154_-267+157del	NM_001287585.2:c.-267+155_-267+157del	NM_001287585.2:c.-267+156_-267+157del	NM_001287585.2:c.-267+157del	NM_001287585.2:c.-267+157dup	NM_001287585.2:c.-267+156_-267+157dup
NUP35 transcript	NM_138285.3:c.211+143=	NM_138285.3:c.211+154_211+157del	NM_138285.3:c.211+155_211+157del	NM_138285.3:c.211+156_211+157del	NM_138285.3:c.211+157del	NM_138285.3:c.211+157dup	NM_138285.3:c.211+156_211+157dup
NUP35 transcript variant 1	NM_138285.5:c.211+143=	NM_138285.5:c.211+154_211+157del	NM_138285.5:c.211+155_211+157del	NM_138285.5:c.211+156_211+157del	NM_138285.5:c.211+157del	NM_138285.5:c.211+157dup	NM_138285.5:c.211+156_211+157dup
NUP35 transcript variant X1	XM_005246284.1:c.220+143=	XM_005246284.1:c.220+154_220+157del	XM_005246284.1:c.220+155_220+157del	XM_005246284.1:c.220+156_220+157del	XM_005246284.1:c.220+157del	XM_005246284.1:c.220+157dup	XM_005246284.1:c.220+156_220+157dup
NUP35 transcript variant X2	XM_005246285.1:c.160+143=	XM_005246285.1:c.160+154_160+157del	XM_005246285.1:c.160+155_160+157del	XM_005246285.1:c.160+156_160+157del	XM_005246285.1:c.160+157del	XM_005246285.1:c.160+157dup	XM_005246285.1:c.160+156_160+157dup
NUP35 transcript variant X3	XM_005246286.1:c.-267+143=	XM_005246286.1:c.-267+154_-267+157del	XM_005246286.1:c.-267+155_-267+157del	XM_005246286.1:c.-267+156_-267+157del	XM_005246286.1:c.-267+157del	XM_005246286.1:c.-267+157dup	XM_005246286.1:c.-267+156_-267+157dup
NUP35 transcript variant X2	XM_006712254.4:c.160+143=	XM_006712254.4:c.160+154_160+157del	XM_006712254.4:c.160+155_160+157del	XM_006712254.4:c.160+156_160+157del	XM_006712254.4:c.160+157del	XM_006712254.4:c.160+157dup	XM_006712254.4:c.160+156_160+157dup
NUP35 transcript variant X5	XM_011510576.4:c.160+143=	XM_011510576.4:c.160+154_160+157del	XM_011510576.4:c.160+155_160+157del	XM_011510576.4:c.160+156_160+157del	XM_011510576.4:c.160+157del	XM_011510576.4:c.160+157dup	XM_011510576.4:c.160+156_160+157dup
NUP35 transcript variant X3	XM_011510577.3:c.160+143=	XM_011510577.3:c.160+154_160+157del	XM_011510577.3:c.160+155_160+157del	XM_011510577.3:c.160+156_160+157del	XM_011510577.3:c.160+157del	XM_011510577.3:c.160+157dup	XM_011510577.3:c.160+156_160+157dup
NUP35 transcript variant X1	XM_017003308.1:c.220+143=	XM_017003308.1:c.220+154_220+157del	XM_017003308.1:c.220+155_220+157del	XM_017003308.1:c.220+156_220+157del	XM_017003308.1:c.220+157del	XM_017003308.1:c.220+157dup	XM_017003308.1:c.220+156_220+157dup
NUP35 transcript variant X4	XM_047443270.1:c.160+143=	XM_047443270.1:c.160+154_160+157del	XM_047443270.1:c.160+155_160+157del	XM_047443270.1:c.160+156_160+157del	XM_047443270.1:c.160+157del	XM_047443270.1:c.160+157dup	XM_047443270.1:c.160+156_160+157dup

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#.

48 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41586566	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss96733900	Feb 13, 2009 (137)
3	BL	ss255969232	May 09, 2011 (137)
4	GMI	ss287711752	May 09, 2011 (137)
5	GMI	ss288263562	May 04, 2012 (137)
6	SSMP	ss663265415	Apr 01, 2015 (144)
7	BILGI_BIOE	ss666178756	Apr 25, 2013 (138)
8	1000GENOMES	ss1369286572	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1703314675	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1703314676	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710042208	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710042234	Apr 01, 2015 (144)
13	SWEGEN	ss2990996873	Nov 08, 2017 (151)
14	MCHAISSO	ss3065782638	Nov 08, 2017 (151)
15	BEROUKHIMLAB	ss3644108651	Oct 11, 2018 (152)
16	URBANLAB	ss3647225124	Oct 11, 2018 (152)
17	EVA_DECODE	ss3705581987	Jul 13, 2019 (153)
18	EVA_DECODE	ss3705581988	Jul 13, 2019 (153)
19	EVA_DECODE	ss3705581989	Jul 13, 2019 (153)
20	EVA_DECODE	ss3705581990	Jul 13, 2019 (153)
21	ACPOP	ss3729179148	Jul 13, 2019 (153)
22	ACPOP	ss3729179149	Jul 13, 2019 (153)
23	PACBIO	ss3784089159	Jul 13, 2019 (153)
24	PACBIO	ss3789637330	Jul 13, 2019 (153)
25	PACBIO	ss3794510445	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3802175225	Jul 13, 2019 (153)
27	EVA	ss3827394503	Apr 25, 2020 (154)
28	EVA	ss3842536576	Apr 25, 2020 (154)
29	GNOMAD	ss4057016639	Apr 26, 2021 (155)
30	GNOMAD	ss4057016640	Apr 26, 2021 (155)
31	GNOMAD	ss4057016641	Apr 26, 2021 (155)
32	GNOMAD	ss4057016642	Apr 26, 2021 (155)
33	GNOMAD	ss4057016643	Apr 26, 2021 (155)
34	GNOMAD	ss4057016644	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5155475499	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5155475500	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5155475501	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5251243668	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5251243669	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5251243670	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5450940166	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5450940167	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5686061982	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5686061983	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5686061984	Oct 12, 2022 (156)
46	YY_MCH	ss5803036284	Oct 12, 2022 (156)
47	EVA	ss5821289097	Oct 12, 2022 (156)
48	EVA	ss5821289098	Oct 12, 2022 (156)
49	1000Genomes	NC_000002.11 - 183993328	Oct 11, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 183993328	Oct 11, 2018 (152)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84189028 (NC_000002.12:183128599::A 322/131272) Row 84189029 (NC_000002.12:183128599::AA 1/131288) Row 84189030 (NC_000002.12:183128599:A: 45340/131036)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84189028 (NC_000002.12:183128599::A 322/131272) Row 84189029 (NC_000002.12:183128599::AA 1/131288) Row 84189030 (NC_000002.12:183128599:A: 45340/131036)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84189028 (NC_000002.12:183128599::A 322/131272) Row 84189029 (NC_000002.12:183128599::AA 1/131288) Row 84189030 (NC_000002.12:183128599:A: 45340/131036)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84189028 (NC_000002.12:183128599::A 322/131272) Row 84189029 (NC_000002.12:183128599::AA 1/131288) Row 84189030 (NC_000002.12:183128599:A: 45340/131036)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84189028 (NC_000002.12:183128599::A 322/131272) Row 84189029 (NC_000002.12:183128599::AA 1/131288) Row 84189030 (NC_000002.12:183128599:A: 45340/131036)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84189028 (NC_000002.12:183128599::A 322/131272) Row 84189029 (NC_000002.12:183128599::AA 1/131288) Row 84189030 (NC_000002.12:183128599:A: 45340/131036)...	-	Apr 26, 2021 (155)
57	Northern Sweden Submission ignored due to conflicting rows: Row 2464013 (NC_000002.11:183993327:A: 141/600) Row 2464014 (NC_000002.11:183993327:AA: 100/600)	-	Jul 13, 2019 (153)
58	Northern Sweden Submission ignored due to conflicting rows: Row 2464013 (NC_000002.11:183993327:A: 141/600) Row 2464014 (NC_000002.11:183993327:AA: 100/600)	-	Jul 13, 2019 (153)
59	8.3KJPN Submission ignored due to conflicting rows: Row 13444806 (NC_000002.11:183993327:A: 3734/16758) Row 13444807 (NC_000002.11:183993327:AA: 201/16758) Row 13444808 (NC_000002.11:183993327::A 9/16758)	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 13444806 (NC_000002.11:183993327:A: 3734/16758) Row 13444807 (NC_000002.11:183993327:AA: 201/16758) Row 13444808 (NC_000002.11:183993327::A 9/16758)	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 13444806 (NC_000002.11:183993327:A: 3734/16758) Row 13444807 (NC_000002.11:183993327:AA: 201/16758) Row 13444808 (NC_000002.11:183993327::A 9/16758)	-	Apr 26, 2021 (155)
62	14KJPN Submission ignored due to conflicting rows: Row 19899086 (NC_000002.12:183128599:A: 6259/28254) Row 19899087 (NC_000002.12:183128599:AA: 328/28254) Row 19899088 (NC_000002.12:183128599::A 21/28254)	-	Oct 12, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 19899086 (NC_000002.12:183128599:A: 6259/28254) Row 19899087 (NC_000002.12:183128599:AA: 328/28254) Row 19899088 (NC_000002.12:183128599::A 21/28254)	-	Oct 12, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 19899086 (NC_000002.12:183128599:A: 6259/28254) Row 19899087 (NC_000002.12:183128599:AA: 328/28254) Row 19899088 (NC_000002.12:183128599::A 21/28254)	-	Oct 12, 2022 (156)
65	UK 10K study - Twins	-	Oct 11, 2018 (152)
66	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6528017 (NC_000002.11:183993327:AA: 626/3708) Row 6528018 (NC_000002.11:183993328:A: 1143/3708)	-	Apr 25, 2020 (154)
67	ALFA	NC_000002.12 - 183128600	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)
rs71407008	May 11, 2012 (137)
rs149840776	May 04, 2012 (137)
rs375742916	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4057016644	NC_000002.12:183128599:AAAA:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3705581990, ss4057016643	NC_000002.12:183128599:AAA:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
14773882532	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
6528017, ss1703314675, ss1703314676, ss2990996873, ss3729179149, ss5155475500, ss5821289098	NC_000002.11:183993327:AA:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3065782638, ss4057016642, ss5251243669, ss5450940167, ss5686061983	NC_000002.12:183128599:AA:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
14773882532	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3705581989	NC_000002.12:183128600:AA:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss255969232, ss288263562	NC_000002.10:183701572:A:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
11813971, ss663265415, ss666178756, ss1369286572, ss3644108651, ss3729179148, ss3784089159, ss3789637330, ss3794510445, ss3827394503, ss5155475499, ss5821289097	NC_000002.11:183993327:A:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1710042208, ss1710042234	NC_000002.11:183993328:A:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3647225124, ss3802175225, ss3842536576, ss4057016641, ss5251243668, ss5450940166, ss5686061982, ss5803036284	NC_000002.12:183128599:A:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
14773882532	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3705581988	NC_000002.12:183128601:A:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss96733900, ss287711752	NT_005403.17:34202745:A:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss41586566	NT_005403.17:34202759:A:	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5155475501	NC_000002.11:183993327::A	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4057016639, ss5251243670, ss5686061984	NC_000002.12:183128599::A	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
14773882532	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3705581987	NC_000002.12:183128602::A	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4057016640	NC_000002.12:183128599::AA	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
14773882532	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000002.12:183128599:AAAAAAAAAAA… NC_000002.12:183128599:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(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 rs34331888

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

rs34331888