Name: rs35297899
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.

rs35297899

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:83046297-83046305 (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=0.115494 (30570/264690, TOPMED)
dupT=0.05605 (864/15416, ALFA)
dupT=0.1922 (861/4480, Estonian) (+ 6 more)
delTT=0.0441 (189/4284, 1000G)
dupT=0.1414 (545/3854, ALSPAC)
dupT=0.1486 (551/3708, TWINSUK)
dupT=0.127 (127/998, GoNL)
dupT=0.123 (74/600, NorthernSweden)
dupT=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: B3GNTL1 : 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	15416	TTTTTTTTT=0.94395	TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTTT=0.05605, TTTTTTTTTTT=0.00000	0.899715	0.011806	0.08848	32
European	Sub	12392	TTTTTTTTT=0.93044	TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTTT=0.06956, TTTTTTTTTTT=0.00000	0.875565	0.014687	0.109748	32
African	Sub	1884	TTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	82	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1802	TTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	88	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	64	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	104	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	520	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	54	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	374	TTTTTTTTT=0.995	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.005, TTTTTTTTTTT=0.000	0.989305	0.0	0.010695	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	- No frequency provided	dupT=0.115494
Allele Frequency Aggregator	Total	Global	15416	(T)₉=0.94395	delTT=0.00000, delT=0.00000, dupT=0.05605, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	12392	(T)₉=0.93044	delTT=0.00000, delT=0.00000, dupT=0.06956, dupTT=0.00000
Allele Frequency Aggregator	African	Sub	1884	(T)₉=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	520	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	374	(T)₉=0.995	delTT=0.000, delT=0.000, dupT=0.005, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	104	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Asian	Sub	88	(T)₉=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	54	(T)₉=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Genetic variation in the Estonian population	Estonian	Study-wide	4480	- No frequency provided	dupT=0.1922
1000Genomes	Global	Study-wide	4284	(T)₉=0.9559	delTT=0.0441
1000Genomes	African	Sub	1201	(T)₉=0.8460	delTT=0.1540
1000Genomes	Europe	Sub	903	(T)₉=1.000	delTT=0.000
1000Genomes	East Asian	Sub	820	(T)₉=1.000	delTT=0.000
1000Genomes	South Asian	Sub	710	(T)₉=1.000	delTT=0.000
1000Genomes	American	Sub	650	(T)₉=0.994	delTT=0.006
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.1414
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.1486
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupT=0.127
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupT=0.123
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.17

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 17	NC_000017.11:g.83046304_83046305del
GRCh38.p14 chr 17	NC_000017.11:g.83046305del
GRCh38.p14 chr 17	NC_000017.11:g.83046305dup
GRCh38.p14 chr 17	NC_000017.11:g.83046304_83046305dup
GRCh37.p13 chr 17	NC_000017.10:g.81004180_81004181del
GRCh37.p13 chr 17	NC_000017.10:g.81004181del
GRCh37.p13 chr 17	NC_000017.10:g.81004181dup
GRCh37.p13 chr 17	NC_000017.10:g.81004180_81004181dup
GRCh38.p14 chr 17 alt locus HSCHR17_1_CTG9	NT_187612.1:g.56637_56638del
GRCh38.p14 chr 17 alt locus HSCHR17_1_CTG9	NT_187612.1:g.56638del
GRCh38.p14 chr 17 alt locus HSCHR17_1_CTG9	NT_187612.1:g.56638dup
GRCh38.p14 chr 17 alt locus HSCHR17_1_CTG9	NT_187612.1:g.56637_56638dup

Gene: B3GNTL1, UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
B3GNTL1 transcript variant 1	NM_001009905.3:c.232+2173… NM_001009905.3:c.232+2173_232+2174del	N/A	Intron Variant
B3GNTL1 transcript variant 2	NM_001320742.2:c.235+2173… NM_001320742.2:c.235+2173_235+2174del	N/A	Intron Variant
B3GNTL1 transcript variant 3	NM_001320743.2:c.	N/A	Genic Upstream Transcript Variant
B3GNTL1 transcript variant 4	NR_135465.2:n.	N/A	Intron Variant
B3GNTL1 transcript variant 5	NR_135466.2:n.	N/A	Genic Upstream Transcript Variant
B3GNTL1 transcript variant X9	XM_006722274.3:c.232+2173… XM_006722274.3:c.232+2173_232+2174del	N/A	Intron Variant
B3GNTL1 transcript variant X3	XM_047435393.1:c.235+2173… XM_047435393.1:c.235+2173_235+2174del	N/A	Intron Variant
B3GNTL1 transcript variant X7	XM_047435395.1:c.232+2173… XM_047435395.1:c.232+2173_232+2174del	N/A	Intron Variant
B3GNTL1 transcript variant X10	XM_047435396.1:c.232+2173… XM_047435396.1:c.232+2173_232+2174del	N/A	Intron Variant
B3GNTL1 transcript variant X13	XM_047435398.1:c.-220+217… XM_047435398.1:c.-220+2173_-220+2174del	N/A	Intron Variant
B3GNTL1 transcript variant X12	XM_047435397.1:c.	N/A	Genic Upstream Transcript Variant
B3GNTL1 transcript variant X5	XR_001752429.2:n.	N/A	Intron Variant
B3GNTL1 transcript variant X2	XR_002957963.2:n.	N/A	Intron Variant
B3GNTL1 transcript variant X1	XR_002957964.2:n.	N/A	Intron Variant
B3GNTL1 transcript variant X6	XR_007065266.1:n.	N/A	Intron Variant
B3GNTL1 transcript variant X8	XR_007065267.1:n.	N/A	Intron Variant
B3GNTL1 transcript variant X11	XR_007065268.1:n.	N/A	Intron Variant
B3GNTL1 transcript variant X4	XR_933927.3:n.	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)₉=	delTT	delT	dupT	dupTT
GRCh38.p14 chr 17	NC_000017.11:g.83046297_83046305=	NC_000017.11:g.83046304_83046305del	NC_000017.11:g.83046305del	NC_000017.11:g.83046305dup	NC_000017.11:g.83046304_83046305dup
GRCh37.p13 chr 17	NC_000017.10:g.81004173_81004181=	NC_000017.10:g.81004180_81004181del	NC_000017.10:g.81004181del	NC_000017.10:g.81004181dup	NC_000017.10:g.81004180_81004181dup
GRCh38.p14 chr 17 alt locus HSCHR17_1_CTG9	NT_187612.1:g.56630_56638=	NT_187612.1:g.56637_56638del	NT_187612.1:g.56638del	NT_187612.1:g.56638dup	NT_187612.1:g.56637_56638dup
B3GNTL1 transcript	NM_001009905.1:c.277+2174=	NM_001009905.1:c.277+2173_277+2174del	NM_001009905.1:c.277+2174del	NM_001009905.1:c.277+2174dup	NM_001009905.1:c.277+2173_277+2174dup
B3GNTL1 transcript variant 1	NM_001009905.3:c.232+2174=	NM_001009905.3:c.232+2173_232+2174del	NM_001009905.3:c.232+2174del	NM_001009905.3:c.232+2174dup	NM_001009905.3:c.232+2173_232+2174dup
B3GNTL1 transcript variant 2	NM_001320742.2:c.235+2174=	NM_001320742.2:c.235+2173_235+2174del	NM_001320742.2:c.235+2174del	NM_001320742.2:c.235+2174dup	NM_001320742.2:c.235+2173_235+2174dup
B3GNTL1 transcript variant X9	XM_006722274.3:c.232+2174=	XM_006722274.3:c.232+2173_232+2174del	XM_006722274.3:c.232+2174del	XM_006722274.3:c.232+2174dup	XM_006722274.3:c.232+2173_232+2174dup
B3GNTL1 transcript variant X3	XM_047435393.1:c.235+2174=	XM_047435393.1:c.235+2173_235+2174del	XM_047435393.1:c.235+2174del	XM_047435393.1:c.235+2174dup	XM_047435393.1:c.235+2173_235+2174dup
B3GNTL1 transcript variant X7	XM_047435395.1:c.232+2174=	XM_047435395.1:c.232+2173_232+2174del	XM_047435395.1:c.232+2174del	XM_047435395.1:c.232+2174dup	XM_047435395.1:c.232+2173_232+2174dup
B3GNTL1 transcript variant X10	XM_047435396.1:c.232+2174=	XM_047435396.1:c.232+2173_232+2174del	XM_047435396.1:c.232+2174del	XM_047435396.1:c.232+2174dup	XM_047435396.1:c.232+2173_232+2174dup
B3GNTL1 transcript variant X13	XM_047435398.1:c.-220+2174=	XM_047435398.1:c.-220+2173_-220+2174del	XM_047435398.1:c.-220+2174del	XM_047435398.1:c.-220+2174dup	XM_047435398.1:c.-220+2173_-220+2174dup

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#.

47 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40785812	Mar 14, 2006 (126)
2	HGSV	ss81792962	Dec 04, 2013 (138)
3	BUSHMAN	ss193465223	Jul 04, 2010 (138)
4	BL	ss256187116	May 09, 2011 (135)
5	GMI	ss289342079	May 04, 2012 (138)
6	TISHKOFF	ss554888109	Jan 10, 2018 (151)
7	SSMP	ss664381704	Apr 01, 2015 (144)
8	EVA-GONL	ss993403199	Aug 21, 2014 (142)
9	1000GENOMES	ss1377070523	Jan 10, 2018 (151)
10	1000GENOMES	ss1377070527	Aug 21, 2014 (142)
11	EVA_GENOME_DK	ss1575100415	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1708874223	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1708874247	Apr 01, 2015 (144)
14	HAMMER_LAB	ss1808912242	Jan 10, 2018 (151)
15	JJLAB	ss2031353828	Sep 14, 2016 (149)
16	SWEGEN	ss3016016334	Nov 08, 2017 (151)
17	MCHAISSO	ss3063880393	Nov 08, 2017 (151)
18	MCHAISSO	ss3065666916	Nov 08, 2017 (151)
19	BIOINF_KMB_FNS_UNIBA	ss3645469727	Oct 12, 2018 (152)
20	EGCUT_WGS	ss3682878821	Jul 13, 2019 (153)
21	EVA_DECODE	ss3701055566	Jul 13, 2019 (153)
22	EVA_DECODE	ss3701055567	Jul 13, 2019 (153)
23	ACPOP	ss3742277295	Jul 13, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3820280490	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3820280491	Jul 13, 2019 (153)
26	EVA	ss3835013785	Apr 27, 2020 (154)
27	VINODS	ss4033014476	Apr 26, 2021 (155)
28	GNOMAD	ss4316799573	Apr 26, 2021 (155)
29	GNOMAD	ss4316799574	Apr 26, 2021 (155)
30	GNOMAD	ss4316799575	Apr 26, 2021 (155)
31	GNOMAD	ss4316799576	Apr 26, 2021 (155)
32	TOPMED	ss5046012462	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5223796125	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5223796126	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5304180829	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5304180830	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5497117289	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5497117290	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5780455290	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5780455291	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5780455292	Oct 16, 2022 (156)
42	YY_MCH	ss5816790733	Oct 16, 2022 (156)
43	EVA	ss5834386078	Oct 16, 2022 (156)
44	EVA	ss5834386079	Oct 16, 2022 (156)
45	EVA	ss5851926618	Oct 16, 2022 (156)
46	EVA	ss5952078370	Oct 16, 2022 (156)
47	EVA	ss5980990372	Oct 16, 2022 (156)
48	1000Genomes	NC_000017.10 - 81004173	Oct 12, 2018 (152)
49	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 81004173	Oct 12, 2018 (152)
50	Genetic variation in the Estonian population	NC_000017.10 - 81004173	Oct 12, 2018 (152)
51	The Danish reference pan genome	NC_000017.10 - 81004173	Apr 27, 2020 (154)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515754998 (NC_000017.11:83046296::T 17025/137522) Row 515754999 (NC_000017.11:83046296::TT 3/137598) Row 515755000 (NC_000017.11:83046296:T: 8/137592)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515754998 (NC_000017.11:83046296::T 17025/137522) Row 515754999 (NC_000017.11:83046296::TT 3/137598) Row 515755000 (NC_000017.11:83046296:T: 8/137592)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515754998 (NC_000017.11:83046296::T 17025/137522) Row 515754999 (NC_000017.11:83046296::TT 3/137598) Row 515755000 (NC_000017.11:83046296:T: 8/137592)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515754998 (NC_000017.11:83046296::T 17025/137522) Row 515754999 (NC_000017.11:83046296::TT 3/137598) Row 515755000 (NC_000017.11:83046296:T: 8/137592)...	-	Apr 26, 2021 (155)
56	Genome of the Netherlands Release 5	NC_000017.10 - 81004173	Apr 27, 2020 (154)
57	Northern Sweden	NC_000017.10 - 81004173	Jul 13, 2019 (153)
58	8.3KJPN Submission ignored due to conflicting rows: Row 81765432 (NC_000017.10:81004172::T 2296/16760) Row 81765433 (NC_000017.10:81004172:T: 3/16760)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 81765432 (NC_000017.10:81004172::T 2296/16760) Row 81765433 (NC_000017.10:81004172:T: 3/16760)	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 114292394 (NC_000017.11:83046296::T 3869/28258) Row 114292395 (NC_000017.11:83046296:T: 4/28258) Row 114292396 (NC_000017.11:83046296::TT 1/28258)	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 114292394 (NC_000017.11:83046296::T 3869/28258) Row 114292395 (NC_000017.11:83046296:T: 4/28258) Row 114292396 (NC_000017.11:83046296::TT 1/28258)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 114292394 (NC_000017.11:83046296::T 3869/28258) Row 114292395 (NC_000017.11:83046296:T: 4/28258) Row 114292396 (NC_000017.11:83046296::TT 1/28258)	-	Oct 16, 2022 (156)
63	TopMed	NC_000017.11 - 83046297	Apr 26, 2021 (155)
64	UK 10K study - Twins	NC_000017.10 - 81004173	Oct 12, 2018 (152)
65	ALFA	NC_000017.11 - 83046297	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)
rs56824761	May 15, 2013 (138)
rs113168308	May 11, 2012 (137)
rs144381219	Sep 17, 2011 (135)
rs539876281	Apr 01, 2015 (144)
rs796196240	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
73093839, ss1377070523, ss1808912242	NC_000017.10:81004172:TT:	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTT	(self)
ss554888109	NC_000017.10:81004179:TT:	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTT	(self)
ss3701055566, ss3820280491, ss4316799576, ss5304180830, ss5497117290	NC_000017.11:83046296:TT:	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTT	(self)
7950745766	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTT	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTT	(self)
ss193465223	NT_010663.15:1245123:TT:	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTT	(self)
ss5223796126	NC_000017.10:81004172:T:	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTT	(self)
ss4316799575, ss5780455291	NC_000017.11:83046296:T:	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTT	(self)
7950745766	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTT	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTT	(self)
ss256187116	NC_000017.9:78597461::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
ss289342079	NC_000017.9:78597470::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
40499268, 28617069, 579823, 18040165, 15562160, 40499268, ss664381704, ss993403199, ss1575100415, ss1708874223, ss1708874247, ss2031353828, ss3016016334, ss3682878821, ss3742277295, ss3835013785, ss5223796125, ss5834386078, ss5952078370, ss5980990372	NC_000017.10:81004172::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
ss1377070527	NC_000017.10:81004174::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
261558124, ss3063880393, ss3065666916, ss3645469727, ss4316799573, ss5046012462, ss5304180829, ss5497117289, ss5780455290, ss5816790733, ss5851926618	NC_000017.11:83046296::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
7950745766	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
ss3701055567, ss3820280490	NC_000017.11:83046298::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
ss40785812	NT_010663.15:1245123::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
ss81792962	NT_010663.15:1245132::T	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
ss4033014476	NT_187612.1:56629::A	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTT	(self)
ss5834386079	NC_000017.10:81004172::TT	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTTT
ss4316799574, ss5780455292	NC_000017.11:83046296::TT	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTTT	(self)
7950745766	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296:TTTTTTTTT:TTTTTTTTTTT	NC_000017.11:83046296:TTTTTTTTT:TT… NC_000017.11:83046296: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 rs35297899

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

rs35297899