Name: rs36027759
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.

rs36027759

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:399176-399188 (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 / dupT…
delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00590 (82/13904, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CCDC77 : Intron Variant
LOC105369594 : 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	13904	TTTTTTTTTTTTT=0.99130	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00590, TTTTTTTTTTTTTTT=0.00280, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000	0.988714	0.000434	0.010852	18
European	Sub	11398	TTTTTTTTTTTTT=0.98947	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00719, TTTTTTTTTTTTTTT=0.00333, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000	0.986217	0.00053	0.013253	14
African	Sub	1282	TTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	44	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1238	TTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	70	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	102	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	566	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	80	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	382	TTTTTTTTTTTTT=0.997	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13904	(T)₁₃=0.99130	delTT=0.00000, delT=0.00000, dupT=0.00590, dupTT=0.00280, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	11398	(T)₁₃=0.98947	delTT=0.00000, delT=0.00000, dupT=0.00719, dupTT=0.00333, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	African	Sub	1282	(T)₁₃=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	566	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	382	(T)₁₃=0.997	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.003, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	102	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Asian	Sub	94	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	80	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00

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 12	NC_000012.12:g.399187_399188del
GRCh38.p14 chr 12	NC_000012.12:g.399188del
GRCh38.p14 chr 12	NC_000012.12:g.399188dup
GRCh38.p14 chr 12	NC_000012.12:g.399187_399188dup
GRCh38.p14 chr 12	NC_000012.12:g.399186_399188dup
GRCh38.p14 chr 12	NC_000012.12:g.399185_399188dup
GRCh37.p13 chr 12	NC_000012.11:g.508353_508354del
GRCh37.p13 chr 12	NC_000012.11:g.508354del
GRCh37.p13 chr 12	NC_000012.11:g.508354dup
GRCh37.p13 chr 12	NC_000012.11:g.508353_508354dup
GRCh37.p13 chr 12	NC_000012.11:g.508352_508354dup
GRCh37.p13 chr 12	NC_000012.11:g.508351_508354dup

Gene: CCDC77, coiled-coil domain containing 77 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CCDC77 transcript variant 3	NM_001130147.2:c.-112-632… NM_001130147.2:c.-112-6324_-112-6323del	N/A	Intron Variant
CCDC77 transcript variant 4	NM_001130148.2:c.-59+9701… NM_001130148.2:c.-59+9701_-59+9702del	N/A	Intron Variant
CCDC77 transcript variant 2	NM_001130146.2:c.	N/A	Genic Upstream Transcript Variant
CCDC77 transcript variant 1	NM_032358.4:c.	N/A	Genic Upstream Transcript Variant

Gene: LOC105369594, uncharacterized LOC105369594 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105369594 transcript	XR_007063149.1: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)₁₃=	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 12	NC_000012.12:g.399176_399188=	NC_000012.12:g.399187_399188del	NC_000012.12:g.399188del	NC_000012.12:g.399188dup	NC_000012.12:g.399187_399188dup	NC_000012.12:g.399186_399188dup	NC_000012.12:g.399185_399188dup
GRCh37.p13 chr 12	NC_000012.11:g.508342_508354=	NC_000012.11:g.508353_508354del	NC_000012.11:g.508354del	NC_000012.11:g.508354dup	NC_000012.11:g.508353_508354dup	NC_000012.11:g.508352_508354dup	NC_000012.11:g.508351_508354dup
CCDC77 transcript variant 3	NM_001130147.1:c.-112-6335=	NM_001130147.1:c.-112-6324_-112-6323del	NM_001130147.1:c.-112-6323del	NM_001130147.1:c.-112-6323dup	NM_001130147.1:c.-112-6324_-112-6323dup	NM_001130147.1:c.-112-6325_-112-6323dup	NM_001130147.1:c.-112-6326_-112-6323dup
CCDC77 transcript variant 3	NM_001130147.2:c.-112-6335=	NM_001130147.2:c.-112-6324_-112-6323del	NM_001130147.2:c.-112-6323del	NM_001130147.2:c.-112-6323dup	NM_001130147.2:c.-112-6324_-112-6323dup	NM_001130147.2:c.-112-6325_-112-6323dup	NM_001130147.2:c.-112-6326_-112-6323dup
CCDC77 transcript variant 4	NM_001130148.1:c.-59+9690=	NM_001130148.1:c.-59+9701_-59+9702del	NM_001130148.1:c.-59+9702del	NM_001130148.1:c.-59+9702dup	NM_001130148.1:c.-59+9701_-59+9702dup	NM_001130148.1:c.-59+9700_-59+9702dup	NM_001130148.1:c.-59+9699_-59+9702dup
CCDC77 transcript variant 4	NM_001130148.2:c.-59+9690=	NM_001130148.2:c.-59+9701_-59+9702del	NM_001130148.2:c.-59+9702del	NM_001130148.2:c.-59+9702dup	NM_001130148.2:c.-59+9701_-59+9702dup	NM_001130148.2:c.-59+9700_-59+9702dup	NM_001130148.2:c.-59+9699_-59+9702dup

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, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40160654	Mar 15, 2006 (126)
2	BUSHMAN	ss193259918	Jul 04, 2010 (132)
3	SSIP	ss947289159	Aug 21, 2014 (142)
4	SYSTEMSBIOZJU	ss2627977972	Nov 08, 2017 (151)
5	SWEGEN	ss3009068137	Nov 08, 2017 (151)
6	SWEGEN	ss3009068138	Nov 08, 2017 (151)
7	ACPOP	ss3738696915	Jul 13, 2019 (153)
8	ACPOP	ss3738696916	Jul 13, 2019 (153)
9	EVA	ss3832930328	Apr 26, 2020 (154)
10	KOGIC	ss3971110004	Apr 26, 2020 (154)
11	KOGIC	ss3971110005	Apr 26, 2020 (154)
12	KOGIC	ss3971110006	Apr 26, 2020 (154)
13	GNOMAD	ss4245607963	Apr 26, 2021 (155)
14	GNOMAD	ss4245607964	Apr 26, 2021 (155)
15	GNOMAD	ss4245607965	Apr 26, 2021 (155)
16	GNOMAD	ss4245607966	Apr 26, 2021 (155)
17	GNOMAD	ss4245607967	Apr 26, 2021 (155)
18	GNOMAD	ss4245607968	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5204691020	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5204691021	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5204691022	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5204691023	Apr 26, 2021 (155)
23	1000G_HIGH_COVERAGE	ss5289521151	Oct 16, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5289521152	Oct 16, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5289521154	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5289521155	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5484445830	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5484445831	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5484445832	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5484445833	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5753370526	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5753370528	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5753370529	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5753370530	Oct 16, 2022 (156)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 397010758 (NC_000012.12:399175::T 12844/135268) Row 397010759 (NC_000012.12:399175::TT 3201/135430) Row 397010760 (NC_000012.12:399175::TTT 1437/135430)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 397010758 (NC_000012.12:399175::T 12844/135268) Row 397010759 (NC_000012.12:399175::TT 3201/135430) Row 397010760 (NC_000012.12:399175::TTT 1437/135430)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 397010758 (NC_000012.12:399175::T 12844/135268) Row 397010759 (NC_000012.12:399175::TT 3201/135430) Row 397010760 (NC_000012.12:399175::TTT 1437/135430)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 397010758 (NC_000012.12:399175::T 12844/135268) Row 397010759 (NC_000012.12:399175::TT 3201/135430) Row 397010760 (NC_000012.12:399175::TTT 1437/135430)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 397010758 (NC_000012.12:399175::T 12844/135268) Row 397010759 (NC_000012.12:399175::TT 3201/135430) Row 397010760 (NC_000012.12:399175::TTT 1437/135430)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 397010758 (NC_000012.12:399175::T 12844/135268) Row 397010759 (NC_000012.12:399175::TT 3201/135430) Row 397010760 (NC_000012.12:399175::TTT 1437/135430)...	-	Apr 26, 2021 (155)
41	Korean Genome Project Submission ignored due to conflicting rows: Row 27488005 (NC_000012.12:399175:T: 30/1832) Row 27488006 (NC_000012.12:399176::TT 93/1832) Row 27488007 (NC_000012.12:399176::T 88/1832)	-	Apr 26, 2020 (154)
42	Korean Genome Project Submission ignored due to conflicting rows: Row 27488005 (NC_000012.12:399175:T: 30/1832) Row 27488006 (NC_000012.12:399176::TT 93/1832) Row 27488007 (NC_000012.12:399176::T 88/1832)	-	Apr 26, 2020 (154)
43	Korean Genome Project Submission ignored due to conflicting rows: Row 27488005 (NC_000012.12:399175:T: 30/1832) Row 27488006 (NC_000012.12:399176::TT 93/1832) Row 27488007 (NC_000012.12:399176::T 88/1832)	-	Apr 26, 2020 (154)
44	Northern Sweden Submission ignored due to conflicting rows: Row 11981780 (NC_000012.11:508341::T 12/600) Row 11981781 (NC_000012.11:508341::TT 3/600)	-	Jul 13, 2019 (153)
45	Northern Sweden Submission ignored due to conflicting rows: Row 11981780 (NC_000012.11:508341::T 12/600) Row 11981781 (NC_000012.11:508341::TT 3/600)	-	Jul 13, 2019 (153)
46	8.3KJPN Submission ignored due to conflicting rows: Row 62660327 (NC_000012.11:508341::TT 2038/16760) Row 62660328 (NC_000012.11:508341::T 463/16760) Row 62660329 (NC_000012.11:508341:T: 4/16760)...	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 62660327 (NC_000012.11:508341::TT 2038/16760) Row 62660328 (NC_000012.11:508341::T 463/16760) Row 62660329 (NC_000012.11:508341:T: 4/16760)...	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 62660327 (NC_000012.11:508341::TT 2038/16760) Row 62660328 (NC_000012.11:508341::T 463/16760) Row 62660329 (NC_000012.11:508341:T: 4/16760)...	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 62660327 (NC_000012.11:508341::TT 2038/16760) Row 62660328 (NC_000012.11:508341::T 463/16760) Row 62660329 (NC_000012.11:508341:T: 4/16760)...	-	Apr 26, 2021 (155)
50	14KJPN Submission ignored due to conflicting rows: Row 87207630 (NC_000012.12:399175::T 784/28258) Row 87207632 (NC_000012.12:399175::TT 3483/28258) Row 87207633 (NC_000012.12:399175:T: 8/28258)...	-	Oct 16, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 87207630 (NC_000012.12:399175::T 784/28258) Row 87207632 (NC_000012.12:399175::TT 3483/28258) Row 87207633 (NC_000012.12:399175:T: 8/28258)...	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 87207630 (NC_000012.12:399175::T 784/28258) Row 87207632 (NC_000012.12:399175::TT 3483/28258) Row 87207633 (NC_000012.12:399175:T: 8/28258)...	-	Oct 16, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 87207630 (NC_000012.12:399175::T 784/28258) Row 87207632 (NC_000012.12:399175::TT 3483/28258) Row 87207633 (NC_000012.12:399175:T: 8/28258)...	-	Oct 16, 2022 (156)
54	ALFA	NC_000012.12 - 399176	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4245607968	NC_000012.12:399175:TT:	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
6301245087	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5204691022	NC_000012.11:508341:T:	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3971110004, ss4245607967, ss5289521155, ss5484445833, ss5753370529	NC_000012.12:399175:T:	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
6301245087	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss947289159, ss2627977972, ss3009068137, ss3738696915, ss3832930328, ss5204691021	NC_000012.11:508341::T	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4245607963, ss5289521151, ss5484445830, ss5753370526	NC_000012.12:399175::T	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6301245087	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3971110006	NC_000012.12:399176::T	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss193259918	NT_009759.17:389175::T	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3009068138, ss3738696916, ss5204691020	NC_000012.11:508341::TT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4245607964, ss5289521152, ss5484445831, ss5753370528	NC_000012.12:399175::TT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6301245087	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3971110005	NC_000012.12:399176::TT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5204691023	NC_000012.11:508341::TTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4245607965, ss5289521154, ss5484445832, ss5753370530	NC_000012.12:399175::TTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6301245087	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss40160654	NT_009759.16:448354::TTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4245607966	NC_000012.12:399175::TTTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6301245087	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000012.12:399175:TTTTTTTTTTTTT:… NC_000012.12:399175:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(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 rs36027759

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

rs36027759