Name: rs35890311
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.

rs35890311

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:55982752-55982767 (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)₆ / delAAA / delAA / delA / …
del(A)₆ / delAAA / delAA / delA / dupA / dupAA / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.10280 (1132/11012, ALFA)
delA=0.2664 (1334/5008, 1000G)
delA=0.335 (197/588, NorthernSweden) (+ 1 more)
delA=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NIPSNAP2 : 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	11012	AAAAAAAAAAAAAAAA=0.89720	AAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.10280, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000	0.819161	0.024818	0.156022	32
European	Sub	7988	AAAAAAAAAAAAAAAA=0.8587	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.1413, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	0.751008	0.034274	0.214718	29
African	Sub	2278	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	94	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	2184	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	80	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	66	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	76	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	254	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	298	AAAAAAAAAAAAAAAA=0.990	AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.010, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	0.979866	0.0	0.020134	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	11012	(A)₁₆=0.89720	del(A)₆=0.00000, delAA=0.00000, delA=0.10280, dupA=0.00000, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	7988	(A)₁₆=0.8587	del(A)₆=0.0000, delAA=0.0000, delA=0.1413, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	2278	(A)₁₆=1.0000	del(A)₆=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Other	Sub	298	(A)₁₆=0.990	del(A)₆=0.000, delAA=0.000, delA=0.010, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	254	(A)₁₆=1.000	del(A)₆=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	80	(A)₁₆=1.00	del(A)₆=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	76	(A)₁₆=1.00	del(A)₆=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	38	(A)₁₆=1.00	del(A)₆=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₆=0.7336	delA=0.2664
1000Genomes	African	Sub	1322	(A)₁₆=0.8343	delA=0.1657
1000Genomes	East Asian	Sub	1008	(A)₁₆=0.8036	delA=0.1964
1000Genomes	Europe	Sub	1006	(A)₁₆=0.6262	delA=0.3738
1000Genomes	South Asian	Sub	978	(A)₁₆=0.676	delA=0.324
1000Genomes	American	Sub	694	(A)₁₆=0.677	delA=0.323
Northern Sweden	ACPOP	Study-wide	588	(A)₁₆=0.665	delA=0.335
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₆=0.65	delA=0.35

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 7	NC_000007.14:g.55982762_55982767del
GRCh38.p14 chr 7	NC_000007.14:g.55982765_55982767del
GRCh38.p14 chr 7	NC_000007.14:g.55982766_55982767del
GRCh38.p14 chr 7	NC_000007.14:g.55982767del
GRCh38.p14 chr 7	NC_000007.14:g.55982767dup
GRCh38.p14 chr 7	NC_000007.14:g.55982766_55982767dup
GRCh38.p14 chr 7	NC_000007.14:g.55982760_55982767dup
GRCh37.p13 chr 7	NC_000007.13:g.56050455_56050460del
GRCh37.p13 chr 7	NC_000007.13:g.56050458_56050460del
GRCh37.p13 chr 7	NC_000007.13:g.56050459_56050460del
GRCh37.p13 chr 7	NC_000007.13:g.56050460del
GRCh37.p13 chr 7	NC_000007.13:g.56050460dup
GRCh37.p13 chr 7	NC_000007.13:g.56050459_56050460dup
GRCh37.p13 chr 7	NC_000007.13:g.56050453_56050460dup

Gene: NIPSNAP2, nipsnap homolog 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NIPSNAP2 transcript variant 2	NM_001202469.2:c.328-966_… NM_001202469.2:c.328-966_328-961del	N/A	Intron Variant
NIPSNAP2 transcript variant 1	NM_001483.3:c.444+482_444… NM_001483.3:c.444+482_444+487del	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)₁₆=	del(A)₆	delAAA	delAA	delA	dupA	dupAA	dup(A)₈
GRCh38.p14 chr 7	NC_000007.14:g.55982752_55982767=	NC_000007.14:g.55982762_55982767del	NC_000007.14:g.55982765_55982767del	NC_000007.14:g.55982766_55982767del	NC_000007.14:g.55982767del	NC_000007.14:g.55982767dup	NC_000007.14:g.55982766_55982767dup	NC_000007.14:g.55982760_55982767dup
GRCh37.p13 chr 7	NC_000007.13:g.56050445_56050460=	NC_000007.13:g.56050455_56050460del	NC_000007.13:g.56050458_56050460del	NC_000007.13:g.56050459_56050460del	NC_000007.13:g.56050460del	NC_000007.13:g.56050460dup	NC_000007.13:g.56050459_56050460dup	NC_000007.13:g.56050453_56050460dup
NIPSNAP2 transcript variant 2	NM_001202469.1:c.328-976=	NM_001202469.1:c.328-966_328-961del	NM_001202469.1:c.328-963_328-961del	NM_001202469.1:c.328-962_328-961del	NM_001202469.1:c.328-961del	NM_001202469.1:c.328-961dup	NM_001202469.1:c.328-962_328-961dup	NM_001202469.1:c.328-968_328-961dup
NIPSNAP2 transcript variant 2	NM_001202469.2:c.328-976=	NM_001202469.2:c.328-966_328-961del	NM_001202469.2:c.328-963_328-961del	NM_001202469.2:c.328-962_328-961del	NM_001202469.2:c.328-961del	NM_001202469.2:c.328-961dup	NM_001202469.2:c.328-962_328-961dup	NM_001202469.2:c.328-968_328-961dup
NIPSNAP2 transcript variant 1	NM_001483.2:c.444+472=	NM_001483.2:c.444+482_444+487del	NM_001483.2:c.444+485_444+487del	NM_001483.2:c.444+486_444+487del	NM_001483.2:c.444+487del	NM_001483.2:c.444+487dup	NM_001483.2:c.444+486_444+487dup	NM_001483.2:c.444+480_444+487dup
NIPSNAP2 transcript variant 1	NM_001483.3:c.444+472=	NM_001483.3:c.444+482_444+487del	NM_001483.3:c.444+485_444+487del	NM_001483.3:c.444+486_444+487del	NM_001483.3:c.444+487del	NM_001483.3:c.444+487dup	NM_001483.3:c.444+486_444+487dup	NM_001483.3:c.444+480_444+487dup

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#.

34 SubSNP, 13 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43094138	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95461551	Dec 05, 2013 (138)
3	BL	ss256066436	May 09, 2011 (137)
4	1000GENOMES	ss1377109975	Aug 21, 2014 (142)
5	EVA_GENOME_DK	ss1576995358	Apr 01, 2015 (144)
6	JJLAB	ss2030842133	Sep 14, 2016 (149)
7	SWEGEN	ss3001163116	Nov 08, 2017 (151)
8	EVA_DECODE	ss3719750226	Jul 13, 2019 (153)
9	EVA_DECODE	ss3719750227	Jul 13, 2019 (153)
10	EVA_DECODE	ss3719750228	Jul 13, 2019 (153)
11	EVA_DECODE	ss3719750229	Jul 13, 2019 (153)
12	EVA_DECODE	ss3719750230	Jul 13, 2019 (153)
13	ACPOP	ss3734659211	Jul 13, 2019 (153)
14	PACBIO	ss3785825973	Jul 13, 2019 (153)
15	PACBIO	ss3791127009	Jul 13, 2019 (153)
16	PACBIO	ss3796006982	Jul 13, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3809760026	Jul 13, 2019 (153)
18	EVA	ss3830589312	Apr 26, 2020 (154)
19	EVA	ss3838784946	Apr 26, 2020 (154)
20	EVA	ss3844237383	Apr 26, 2020 (154)
21	GNOMAD	ss4163901119	Apr 26, 2021 (155)
22	GNOMAD	ss4163901120	Apr 26, 2021 (155)
23	GNOMAD	ss4163901121	Apr 26, 2021 (155)
24	GNOMAD	ss4163901122	Apr 26, 2021 (155)
25	GNOMAD	ss4163901123	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5183268297	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5183268298	Apr 26, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5272974672	Oct 13, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5272974673	Oct 13, 2022 (156)
30	HUGCELL_USP	ss5470135497	Oct 13, 2022 (156)
31	HUGCELL_USP	ss5470135498	Oct 13, 2022 (156)
32	TOMMO_GENOMICS	ss5723138125	Oct 13, 2022 (156)
33	TOMMO_GENOMICS	ss5723138126	Oct 13, 2022 (156)
34	EVA	ss5855908238	Oct 13, 2022 (156)
35	1000Genomes	NC_000007.13 - 56050445	Oct 12, 2018 (152)
36	The Danish reference pan genome	NC_000007.13 - 56050445	Apr 26, 2020 (154)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 262251838 (NC_000007.14:55982751::A 242/104600) Row 262251839 (NC_000007.14:55982751::AA 1/104690) Row 262251840 (NC_000007.14:55982751:A: 30742/104524)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 262251838 (NC_000007.14:55982751::A 242/104600) Row 262251839 (NC_000007.14:55982751::AA 1/104690) Row 262251840 (NC_000007.14:55982751:A: 30742/104524)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 262251838 (NC_000007.14:55982751::A 242/104600) Row 262251839 (NC_000007.14:55982751::AA 1/104690) Row 262251840 (NC_000007.14:55982751:A: 30742/104524)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 262251838 (NC_000007.14:55982751::A 242/104600) Row 262251839 (NC_000007.14:55982751::AA 1/104690) Row 262251840 (NC_000007.14:55982751:A: 30742/104524)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 262251838 (NC_000007.14:55982751::A 242/104600) Row 262251839 (NC_000007.14:55982751::AA 1/104690) Row 262251840 (NC_000007.14:55982751:A: 30742/104524)...	-	Apr 26, 2021 (155)
42	Northern Sweden	NC_000007.13 - 56050445	Jul 13, 2019 (153)
43	8.3KJPN Submission ignored due to conflicting rows: Row 41237604 (NC_000007.13:56050444:A: 1561/16758) Row 41237605 (NC_000007.13:56050444::A 12/16758)	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 41237604 (NC_000007.13:56050444:A: 1561/16758) Row 41237605 (NC_000007.13:56050444::A 12/16758)	-	Apr 26, 2021 (155)
45	14KJPN Submission ignored due to conflicting rows: Row 56975229 (NC_000007.14:55982751:A: 2667/28258) Row 56975230 (NC_000007.14:55982751::A 23/28258)	-	Oct 13, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 56975229 (NC_000007.14:55982751:A: 2667/28258) Row 56975230 (NC_000007.14:55982751::A 23/28258)	-	Oct 13, 2022 (156)
47	ALFA	NC_000007.14 - 55982752	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)
rs71015145	May 11, 2012 (137)
rs146534662	May 04, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
939807249	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3719750230, ss4163901123	NC_000007.14:55982751:AAA:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4163901122	NC_000007.14:55982751:AA:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
939807249	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3719750229	NC_000007.14:55982752:AA:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss256066436	NC_000007.12:56017938:A:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
37214609, 1152771, 7944076, ss1377109975, ss1576995358, ss2030842133, ss3001163116, ss3734659211, ss3785825973, ss3791127009, ss3796006982, ss3830589312, ss3838784946, ss5183268297	NC_000007.13:56050444:A:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3809760026, ss3844237383, ss4163901121, ss5272974672, ss5470135497, ss5723138125, ss5855908238	NC_000007.14:55982751:A:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
939807249	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3719750228	NC_000007.14:55982753:A:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss43094138	NT_033968.6:5639813:A:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss95461551	NT_033968.6:5639828:A:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5183268298	NC_000007.13:56050444::A	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4163901119, ss5272974673, ss5470135498, ss5723138126	NC_000007.14:55982751::A	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
939807249	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3719750227	NC_000007.14:55982754::A	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4163901120	NC_000007.14:55982751::AA	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
939807249	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3719750226	NC_000007.14:55982754::AAAAAAAA	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3530922945	NC_000007.14:55982751:AAAAAA:	NC_000007.14:55982751:AAAAAAAAAAAA… NC_000007.14:55982751:AAAAAAAAAAAAAAAA:AAAAAAAAAA

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

No publications for rs35890311

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

rs35890311