Name: rs35072988
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.

rs35072988

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:39027089-39027097 (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: delGTGT / delGT / dupGT / dupGTGT …
delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃
Variation Type: Indel Insertion and Deletion
Frequency: delGT=0.000015 (4/264690, TOPMED)
dupGTGT=0.17977 (5080/28258, 14KJPN)
dupGTGT=0.17757 (2976/16760, 8.3KJPN) (+ 7 more)
dupGTGT=0.03232 (492/15222, ALFA)
dupGTGT=0.1917 (960/5008, 1000G)
dupGTGT=0.1100 (493/4480, Estonian)
dupGTGT=0.112 (112/998, GoNL)
dupGTGT=0.130 (78/600, NorthernSweden)
dupGTGT=0.236 (50/212, Vietnamese)
dupGTGT=0.10 (4/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PROSER1 : 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	15222	TGTGTGTGT=0.96768	TGTGT=0.00000, TGTGTGT=0.00000, TGTGTGTGTGT=0.00000, TGTGTGTGTGTGT=0.03232, TGTGTGTGTGTGTGT=0.00000	0.93759	0.002234	0.060176	6
European	Sub	12594	TGTGTGTGT=0.96101	TGTGT=0.00000, TGTGTGT=0.00000, TGTGTGTGTGT=0.00000, TGTGTGTGTGTGT=0.03899, TGTGTGTGTGTGTGT=0.00000	0.924726	0.0027	0.072574	4
African	Sub	1538	TGTGTGTGT=1.0000	TGTGT=0.0000, TGTGTGT=0.0000, TGTGTGTGTGT=0.0000, TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	58	TGTGTGTGT=1.00	TGTGT=0.00, TGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1480	TGTGTGTGT=1.0000	TGTGT=0.0000, TGTGTGT=0.0000, TGTGTGTGTGT=0.0000, TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	64	TGTGTGTGT=1.00	TGTGT=0.00, TGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	50	TGTGTGTGT=1.00	TGTGT=0.00, TGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TGTGTGTGT=1.00	TGTGT=0.00, TGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	110	TGTGTGTGT=1.000	TGTGT=0.000, TGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	506	TGTGTGTGT=1.000	TGTGT=0.000, TGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	TGTGTGTGT=1.00	TGTGT=0.00, TGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	352	TGTGTGTGT=0.997	TGTGT=0.000, TGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGT=0.003, TGTGTGTGTGTGTGT=0.000	0.994318	0.0	0.005682	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	(TG)₄T=0.999985	delGT=0.000015
14KJPN	JAPANESE	Study-wide	28258	- No frequency provided	dupGTGT=0.17977
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	dupGTGT=0.17757
Allele Frequency Aggregator	Total	Global	15222	(TG)₄T=0.96768	delGTGT=0.00000, delGT=0.00000, dupGT=0.00000, dupGTGT=0.03232, dup(GT)₃=0.00000
Allele Frequency Aggregator	European	Sub	12594	(TG)₄T=0.96101	delGTGT=0.00000, delGT=0.00000, dupGT=0.00000, dupGTGT=0.03899, dup(GT)₃=0.00000
Allele Frequency Aggregator	African	Sub	1538	(TG)₄T=1.0000	delGTGT=0.0000, delGT=0.0000, dupGT=0.0000, dupGTGT=0.0000, dup(GT)₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	506	(TG)₄T=1.000	delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000
Allele Frequency Aggregator	Other	Sub	352	(TG)₄T=0.997	delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.003, dup(GT)₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	110	(TG)₄T=1.000	delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000
Allele Frequency Aggregator	Asian	Sub	64	(TG)₄T=1.00	delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(TG)₄T=1.00	delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupGTGT=0.1917
1000Genomes	African	Sub	1322	- No frequency provided	dupGTGT=0.2738
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupGTGT=0.2202
1000Genomes	Europe	Sub	1006	- No frequency provided	dupGTGT=0.1193
1000Genomes	South Asian	Sub	978	- No frequency provided	dupGTGT=0.197
1000Genomes	American	Sub	694	- No frequency provided	dupGTGT=0.091
Genetic variation in the Estonian population	Estonian	Study-wide	4480	- No frequency provided	dupGTGT=0.1100
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupGTGT=0.112
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupGTGT=0.130
A Vietnamese Genetic Variation Database	Global	Study-wide	212	- No frequency provided	dupGTGT=0.236
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupGTGT=0.10

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 13	NC_000013.11:g.39027090GT[2]
GRCh38.p14 chr 13	NC_000013.11:g.39027090GT[3]
GRCh38.p14 chr 13	NC_000013.11:g.39027090GT[5]
GRCh38.p14 chr 13	NC_000013.11:g.39027090GT[6]
GRCh38.p14 chr 13	NC_000013.11:g.39027090GT[7]
GRCh37.p13 chr 13	NC_000013.10:g.39601227GT[2]
GRCh37.p13 chr 13	NC_000013.10:g.39601227GT[3]
GRCh37.p13 chr 13	NC_000013.10:g.39601227GT[5]
GRCh37.p13 chr 13	NC_000013.10:g.39601227GT[6]
GRCh37.p13 chr 13	NC_000013.10:g.39601227GT[7]

Gene: PROSER1, proline and serine rich 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PROSER1 transcript variant 1	NM_025138.5:c.370-709CA[2]	N/A	Intron Variant
PROSER1 transcript variant 2	NM_170719.4:c.304-709CA[2]	N/A	Intron Variant
PROSER1 transcript variant X1	XM_011535239.4:c.370-709C… XM_011535239.4:c.370-709CA[2]	N/A	Intron Variant
PROSER1 transcript variant X2	XM_047430652.1:c.304-709C… XM_047430652.1:c.304-709CA[2]	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	(TG)₄T=	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃
GRCh38.p14 chr 13	NC_000013.11:g.39027089_39027097=	NC_000013.11:g.39027090GT[2]	NC_000013.11:g.39027090GT[3]	NC_000013.11:g.39027090GT[5]	NC_000013.11:g.39027090GT[6]	NC_000013.11:g.39027090GT[7]
GRCh37.p13 chr 13	NC_000013.10:g.39601226_39601234=	NC_000013.10:g.39601227GT[2]	NC_000013.10:g.39601227GT[3]	NC_000013.10:g.39601227GT[5]	NC_000013.10:g.39601227GT[6]	NC_000013.10:g.39601227GT[7]
PROSER1 transcript variant 1	NM_025138.4:c.370-702=	NM_025138.4:c.370-709CA[2]	NM_025138.4:c.370-709CA[3]	NM_025138.4:c.370-709CA[5]	NM_025138.4:c.370-709CA[6]	NM_025138.4:c.370-709CA[7]
PROSER1 transcript variant 1	NM_025138.5:c.370-702=	NM_025138.5:c.370-709CA[2]	NM_025138.5:c.370-709CA[3]	NM_025138.5:c.370-709CA[5]	NM_025138.5:c.370-709CA[6]	NM_025138.5:c.370-709CA[7]
PROSER1 transcript variant 2	NM_170719.4:c.304-702=	NM_170719.4:c.304-709CA[2]	NM_170719.4:c.304-709CA[3]	NM_170719.4:c.304-709CA[5]	NM_170719.4:c.304-709CA[6]	NM_170719.4:c.304-709CA[7]
PROSER1 transcript variant X1	XM_005266545.1:c.304-702=	XM_005266545.1:c.304-709CA[2]	XM_005266545.1:c.304-709CA[3]	XM_005266545.1:c.304-709CA[5]	XM_005266545.1:c.304-709CA[6]	XM_005266545.1:c.304-709CA[7]
PROSER1 transcript variant X1	XM_011535239.4:c.370-702=	XM_011535239.4:c.370-709CA[2]	XM_011535239.4:c.370-709CA[3]	XM_011535239.4:c.370-709CA[5]	XM_011535239.4:c.370-709CA[6]	XM_011535239.4:c.370-709CA[7]
PROSER1 transcript variant X2	XM_047430652.1:c.304-702=	XM_047430652.1:c.304-709CA[2]	XM_047430652.1:c.304-709CA[3]	XM_047430652.1:c.304-709CA[5]	XM_047430652.1:c.304-709CA[6]	XM_047430652.1:c.304-709CA[7]

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	ss40291216	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss95943749	Dec 05, 2013 (138)
3	GMI	ss289172634	May 04, 2012 (137)
4	1000GENOMES	ss327517352	May 09, 2011 (135)
5	1000GENOMES	ss327619104	May 09, 2011 (135)
6	1000GENOMES	ss328065455	May 09, 2011 (135)
7	1000GENOMES	ss499956031	May 04, 2012 (137)
8	LUNTER	ss552284209	Apr 25, 2013 (138)
9	LUNTER	ss552588874	Apr 25, 2013 (138)
10	LUNTER	ss553516047	Apr 25, 2013 (138)
11	SSMP	ss664174873	Apr 01, 2015 (144)
12	EVA-GONL	ss990309270	Aug 21, 2014 (142)
13	1000GENOMES	ss1373058048	Aug 21, 2014 (142)
14	DDI	ss1536755554	Apr 01, 2015 (144)
15	EVA_GENOME_DK	ss1574626817	Apr 01, 2015 (144)
16	EVA_DECODE	ss1684829367	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1707754164	Jan 10, 2018 (151)
18	EVA_UK10K_TWINSUK	ss1707754357	Jan 10, 2018 (151)
19	EVA_UK10K_TWINSUK	ss1710598007	Apr 01, 2015 (144)
20	EVA_UK10K_ALSPAC	ss1710598012	Apr 01, 2015 (144)
21	HAMMER_LAB	ss1807576451	Sep 08, 2015 (146)
22	JJLAB	ss2031178595	Sep 14, 2016 (149)
23	SYSTEMSBIOZJU	ss2628287935	Nov 08, 2017 (151)
24	GNOMAD	ss2918772611	Nov 08, 2017 (151)
25	SWEGEN	ss3010893981	Nov 08, 2017 (151)
26	MCHAISSO	ss3065516321	Nov 08, 2017 (151)
27	BEROUKHIMLAB	ss3644357186	Oct 12, 2018 (152)
28	URBANLAB	ss3650015529	Oct 12, 2018 (152)
29	EGCUT_WGS	ss3678158590	Jul 13, 2019 (153)
30	EVA_DECODE	ss3695137837	Jul 13, 2019 (153)
31	ACPOP	ss3739679178	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3816699771	Jul 13, 2019 (153)
33	EVA	ss3833506421	Apr 27, 2020 (154)
34	EVA	ss3840332964	Apr 27, 2020 (154)
35	EVA	ss3845818273	Apr 27, 2020 (154)
36	GNOMAD	ss4264516764	Apr 26, 2021 (155)
37	GNOMAD	ss4264516765	Apr 26, 2021 (155)
38	TOPMED	ss4943580543	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5209644704	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5293464114	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5487856124	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5761419236	Oct 16, 2022 (156)
43	YY_MCH	ss5814042659	Oct 16, 2022 (156)
44	EVA	ss5839369337	Oct 16, 2022 (156)
45	EVA	ss5850694309	Oct 16, 2022 (156)
46	EVA	ss5924797224	Oct 16, 2022 (156)
47	EVA	ss5946029407	Oct 16, 2022 (156)
48	1000Genomes	NC_000013.10 - 39601226	Oct 12, 2018 (152)
49	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33759655 (NC_000013.10:39601225::TGTG 379/3854) Row 33759656 (NC_000013.10:39601225:TG: 1/3854)	-	Oct 12, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33759655 (NC_000013.10:39601225::TGTG 379/3854) Row 33759656 (NC_000013.10:39601225:TG: 1/3854)	-	Oct 12, 2018 (152)
51	Genetic variation in the Estonian population	NC_000013.10 - 39601226	Oct 12, 2018 (152)
52	The Danish reference pan genome	NC_000013.10 - 39601226	Apr 27, 2020 (154)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428501672 (NC_000013.11:39027088::TG 0/139964) Row 428501673 (NC_000013.11:39027088::TGTG 21543/139892) Row 428501675 (NC_000013.11:39027088:TG: 5/139964)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428501672 (NC_000013.11:39027088::TG 0/139964) Row 428501673 (NC_000013.11:39027088::TGTG 21543/139892) Row 428501675 (NC_000013.11:39027088:TG: 5/139964)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428501672 (NC_000013.11:39027088::TG 0/139964) Row 428501673 (NC_000013.11:39027088::TGTG 21543/139892) Row 428501675 (NC_000013.11:39027088:TG: 5/139964)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428501672 (NC_000013.11:39027088::TG 0/139964) Row 428501673 (NC_000013.11:39027088::TGTG 21543/139892) Row 428501675 (NC_000013.11:39027088:TG: 5/139964)...	-	Apr 26, 2021 (155)
57	Genome of the Netherlands Release 5	NC_000013.10 - 39601226	Apr 27, 2020 (154)
58	Northern Sweden	NC_000013.10 - 39601226	Jul 13, 2019 (153)
59	8.3KJPN	NC_000013.10 - 39601226	Apr 26, 2021 (155)
60	14KJPN	NC_000013.11 - 39027089	Oct 16, 2022 (156)
61	TopMed	NC_000013.11 - 39027089	Apr 26, 2021 (155)
62	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33759655 (NC_000013.10:39601225::TGTG 369/3708) Row 33759656 (NC_000013.10:39601225:TG: 0/3708)	-	Oct 12, 2018 (152)
63	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33759655 (NC_000013.10:39601225::TGTG 369/3708) Row 33759656 (NC_000013.10:39601225:TG: 0/3708)	-	Oct 12, 2018 (152)
64	A Vietnamese Genetic Variation Database	NC_000013.10 - 39601226	Jul 13, 2019 (153)
65	ALFA	NC_000013.11 - 39027089	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)
rs375102922	May 15, 2013 (138)
rs796361622	Nov 08, 2017 (151)
rs146908814	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4264516765	NC_000013.11:39027088:TGTG:	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGT	(self)
10797692496	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGT	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGT	(self)
ss1707754164, ss1707754357	NC_000013.10:39601225:TG:	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGT	(self)
159126201, ss4264516764, ss4943580543	NC_000013.11:39027088:TG:	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGT	(self)
10797692496	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGT	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGT	(self)
	NC_000013.11:39027088::TG	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGT	(self)
10797692496	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGT	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGT	(self)
ss327517352, ss327619104, ss328065455, ss552284209, ss552588874, ss553516047, ss1684829367	NC_000013.9:38499225::TGTG	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
ss289172634	NC_000013.9:38499234::GTGT	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
60774442, 23896838, 400004, 15063924, 12964043, 67614011, 7489241, ss499956031, ss664174873, ss990309270, ss1373058048, ss1536755554, ss1574626817, ss1807576451, ss2031178595, ss2628287935, ss2918772611, ss3010893981, ss3644357186, ss3678158590, ss3739679178, ss3833506421, ss3840332964, ss5209644704, ss5839369337, ss5946029407	NC_000013.10:39601225::TGTG	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
ss1710598007, ss1710598012	NC_000013.10:39601227::TGTG	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
95256340, ss3065516321, ss3650015529, ss3695137837, ss3816699771, ss3845818273, ss5293464114, ss5487856124, ss5761419236, ss5814042659, ss5850694309, ss5924797224	NC_000013.11:39027088::TGTG	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
10797692496	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
ss40291216	NT_024524.14:20581225::TGTG	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
ss95943749	NT_024524.14:20581234::GTGT	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGT	(self)
10797692496	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGTGT	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGTGT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3190678779	NC_000013.11:39027088::TGTGTG	NC_000013.11:39027088:TGTGTGTGT:TG… NC_000013.11:39027088:TGTGTGTGT:TGTGTGTGTGTGTGT

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

No publications for rs35072988

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
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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

rs35072988