Name: rs59953663
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.

rs59953663

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:63820432-63820444 (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: delAT / dupAT / dupATAT / dup(AT)₃
Variation Type: Indel Insertion and Deletion
Frequency: dupAT=0.01452 (215/14804, ALFA)
dupAT=0.0473 (212/4480, Estonian)
dupAT=0.088 (88/998, GoNL) (+ 2 more)
dupAT=0.080 (48/600, NorthernSweden)
dupAT=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZBTB46 : Intron Variant
ZBTB46-AS1 : 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	14804	TATATATATATAT=0.98548	TATATATATATATAT=0.01452, TATATATATATATATAT=0.00000, TATATATATATATATATAT=0.00000	0.971899	0.000946	0.027155	11
European	Sub	11102	TATATATATATAT=0.98072	TATATATATATATAT=0.01928, TATATATATATATATAT=0.00000, TATATATATATATATATAT=0.00000	0.962709	0.001261	0.03603	7
African	Sub	2598	TATATATATATAT=1.0000	TATATATATATATAT=0.0000, TATATATATATATATAT=0.0000, TATATATATATATATATAT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	108	TATATATATATAT=1.000	TATATATATATATAT=0.000, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
African American	Sub	2490	TATATATATATAT=1.0000	TATATATATATATAT=0.0000, TATATATATATATATAT=0.0000, TATATATATATATATATAT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	36	TATATATATATAT=1.00	TATATATATATATAT=0.00, TATATATATATATATAT=0.00, TATATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TATATATATATAT=1.00	TATATATATATATAT=0.00, TATATATATATATATAT=0.00, TATATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TATATATATATAT=1.0	TATATATATATATAT=0.0, TATATATATATATATAT=0.0, TATATATATATATATATAT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	132	TATATATATATAT=1.000	TATATATATATATAT=0.000, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	452	TATATATATATAT=1.000	TATATATATATATAT=0.000, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	72	TATATATATATAT=1.00	TATATATATATATAT=0.00, TATATATATATATATAT=0.00, TATATATATATATATATAT=0.00	1.0	0.0	0.0	N/A
Other	Sub	412	TATATATATATAT=0.998	TATATATATATATAT=0.002, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000	0.995146	0.0	0.004854	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	14804	(TA)₆T=0.98548	dupAT=0.01452, dupATAT=0.00000, dup(AT)₃=0.00000
Allele Frequency Aggregator	European	Sub	11102	(TA)₆T=0.98072	dupAT=0.01928, dupATAT=0.00000, dup(AT)₃=0.00000
Allele Frequency Aggregator	African	Sub	2598	(TA)₆T=1.0000	dupAT=0.0000, dupATAT=0.0000, dup(AT)₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	452	(TA)₆T=1.000	dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000
Allele Frequency Aggregator	Other	Sub	412	(TA)₆T=0.998	dupAT=0.002, dupATAT=0.000, dup(AT)₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	132	(TA)₆T=1.000	dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000
Allele Frequency Aggregator	South Asian	Sub	72	(TA)₆T=1.00	dupAT=0.00, dupATAT=0.00, dup(AT)₃=0.00
Allele Frequency Aggregator	Asian	Sub	36	(TA)₆T=1.00	dupAT=0.00, dupATAT=0.00, dup(AT)₃=0.00
Genetic variation in the Estonian population	Estonian	Study-wide	4480	- No frequency provided	dupAT=0.0473
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupAT=0.088
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupAT=0.080
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupAT=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 20	NC_000020.11:g.63820433AT[5]
GRCh38.p14 chr 20	NC_000020.11:g.63820433AT[7]
GRCh38.p14 chr 20	NC_000020.11:g.63820433AT[8]
GRCh38.p14 chr 20	NC_000020.11:g.63820433AT[9]
GRCh37.p13 chr 20	NC_000020.10:g.62451786AT[5]
GRCh37.p13 chr 20	NC_000020.10:g.62451786AT[7]
GRCh37.p13 chr 20	NC_000020.10:g.62451786AT[8]
GRCh37.p13 chr 20	NC_000020.10:g.62451786AT[9]

Gene: ZBTB46, zinc finger and BTB domain containing 46 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZBTB46 transcript variant 1	NM_001369741.1:c.-34+1065… NM_001369741.1:c.-34+10654TA[5]	N/A	Intron Variant
ZBTB46 transcript variant 2	NM_025224.4:c.	N/A	Genic Upstream Transcript Variant
ZBTB46 transcript variant X2	XM_005260197.5:c.-34+1150… XM_005260197.5:c.-34+11506TA[5]	N/A	Intron Variant
ZBTB46 transcript variant X5	XM_005260198.5:c.-34+1025… XM_005260198.5:c.-34+10255TA[5]	N/A	Intron Variant
ZBTB46 transcript variant X4	XM_006723700.4:c.-34+1011… XM_006723700.4:c.-34+10114TA[5]	N/A	Intron Variant
ZBTB46 transcript variant X1	XM_011528548.3:c.-34+1154… XM_011528548.3:c.-34+11542TA[5]	N/A	Intron Variant
ZBTB46 transcript variant X10	XM_011528549.3:c.-34+1065… XM_011528549.3:c.-34+10654TA[5]	N/A	Intron Variant
ZBTB46 transcript variant X9	XM_017027667.2:c.-34+1065… XM_017027667.2:c.-34+10654TA[5]	N/A	Intron Variant
ZBTB46 transcript variant X7	XM_047439901.1:c.-34+3676… XM_047439901.1:c.-34+3676TA[5]	N/A	Intron Variant
ZBTB46 transcript variant X6	XM_005260195.5:c.	N/A	Genic Upstream Transcript Variant
ZBTB46 transcript variant X8	XR_001754167.2:n.	N/A	Intron Variant
ZBTB46 transcript variant X3	XR_936500.3:n.	N/A	Intron Variant

Gene: ZBTB46-AS1, ZBTB46 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZBTB46-AS1 transcript	NR_110081.1: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	(TA)₆T=	delAT	dupAT	dupATAT	dup(AT)₃
GRCh38.p14 chr 20	NC_000020.11:g.63820432_63820444=	NC_000020.11:g.63820433AT[5]	NC_000020.11:g.63820433AT[7]	NC_000020.11:g.63820433AT[8]	NC_000020.11:g.63820433AT[9]
GRCh37.p13 chr 20	NC_000020.10:g.62451785_62451797=	NC_000020.10:g.62451786AT[5]	NC_000020.10:g.62451786AT[7]	NC_000020.10:g.62451786AT[8]	NC_000020.10:g.62451786AT[9]
ZBTB46 transcript variant 1	NM_001369741.1:c.-34+10665=	NM_001369741.1:c.-34+10654TA[5]	NM_001369741.1:c.-34+10654TA[7]	NM_001369741.1:c.-34+10654TA[8]	NM_001369741.1:c.-34+10654TA[9]
ZBTB46 transcript variant X2	XM_005260196.1:c.-34+10665=	XM_005260196.1:c.-34+10654TA[5]	XM_005260196.1:c.-34+10654TA[7]	XM_005260196.1:c.-34+10654TA[8]	XM_005260196.1:c.-34+10654TA[9]
ZBTB46 transcript variant X3	XM_005260197.1:c.-34+11517=	XM_005260197.1:c.-34+11506TA[5]	XM_005260197.1:c.-34+11506TA[7]	XM_005260197.1:c.-34+11506TA[8]	XM_005260197.1:c.-34+11506TA[9]
ZBTB46 transcript variant X2	XM_005260197.5:c.-34+11517=	XM_005260197.5:c.-34+11506TA[5]	XM_005260197.5:c.-34+11506TA[7]	XM_005260197.5:c.-34+11506TA[8]	XM_005260197.5:c.-34+11506TA[9]
ZBTB46 transcript variant X4	XM_005260198.1:c.-34+10266=	XM_005260198.1:c.-34+10255TA[5]	XM_005260198.1:c.-34+10255TA[7]	XM_005260198.1:c.-34+10255TA[8]	XM_005260198.1:c.-34+10255TA[9]
ZBTB46 transcript variant X5	XM_005260198.5:c.-34+10266=	XM_005260198.5:c.-34+10255TA[5]	XM_005260198.5:c.-34+10255TA[7]	XM_005260198.5:c.-34+10255TA[8]	XM_005260198.5:c.-34+10255TA[9]
ZBTB46 transcript variant X4	XM_006723700.4:c.-34+10125=	XM_006723700.4:c.-34+10114TA[5]	XM_006723700.4:c.-34+10114TA[7]	XM_006723700.4:c.-34+10114TA[8]	XM_006723700.4:c.-34+10114TA[9]
ZBTB46 transcript variant X1	XM_011528548.3:c.-34+11553=	XM_011528548.3:c.-34+11542TA[5]	XM_011528548.3:c.-34+11542TA[7]	XM_011528548.3:c.-34+11542TA[8]	XM_011528548.3:c.-34+11542TA[9]
ZBTB46 transcript variant X10	XM_011528549.3:c.-34+10665=	XM_011528549.3:c.-34+10654TA[5]	XM_011528549.3:c.-34+10654TA[7]	XM_011528549.3:c.-34+10654TA[8]	XM_011528549.3:c.-34+10654TA[9]
ZBTB46 transcript variant X9	XM_017027667.2:c.-34+10665=	XM_017027667.2:c.-34+10654TA[5]	XM_017027667.2:c.-34+10654TA[7]	XM_017027667.2:c.-34+10654TA[8]	XM_017027667.2:c.-34+10654TA[9]
ZBTB46 transcript variant X7	XM_047439901.1:c.-34+3687=	XM_047439901.1:c.-34+3676TA[5]	XM_047439901.1:c.-34+3676TA[7]	XM_047439901.1:c.-34+3676TA[8]	XM_047439901.1:c.-34+3676TA[9]

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#.

41 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80989807	Dec 04, 2013 (138)
2	GMI	ss289421083	May 04, 2012 (137)
3	1000GENOMES	ss327964581	May 09, 2011 (134)
4	1000GENOMES	ss499744736	May 04, 2012 (137)
5	LUNTER	ss552677684	Apr 25, 2013 (138)
6	LUNTER	ss553686197	Apr 25, 2013 (138)
7	SSMP	ss664488982	Apr 01, 2015 (144)
8	SSIP	ss947407452	Aug 21, 2014 (142)
9	EVA-GONL	ss994911749	Aug 21, 2014 (142)
10	EVA_GENOME_DK	ss1575739012	Apr 01, 2015 (144)
11	EVA_DECODE	ss1698976423	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1709428620	Jan 10, 2018 (151)
13	EVA_UK10K_TWINSUK	ss1709428636	Jan 10, 2018 (151)
14	EVA_UK10K_ALSPAC	ss1710822697	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1710822698	Apr 01, 2015 (144)
16	JJLAB	ss2031442073	Sep 14, 2016 (149)
17	SWEGEN	ss3018480894	Nov 08, 2017 (151)
18	MCHAISSO	ss3064005018	Nov 08, 2017 (151)
19	EGCUT_WGS	ss3685165852	Jul 13, 2019 (153)
20	EVA_DECODE	ss3707320650	Jul 13, 2019 (153)
21	EVA_DECODE	ss3707320651	Jul 13, 2019 (153)
22	EVA_DECODE	ss3707320652	Jul 13, 2019 (153)
23	ACPOP	ss3743555475	Jul 13, 2019 (153)
24	EVA	ss3835767037	Apr 27, 2020 (154)
25	EVA	ss3841508455	Apr 27, 2020 (154)
26	EVA	ss3847022296	Apr 27, 2020 (154)
27	GNOMAD	ss4356509550	Apr 27, 2021 (155)
28	GNOMAD	ss4356509551	Apr 27, 2021 (155)
29	GNOMAD	ss4356509552	Apr 27, 2021 (155)
30	GNOMAD	ss4356509554	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5230485291	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5230485292	Apr 27, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5309449317	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5309449318	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5501663275	Oct 16, 2022 (156)
36	SANFORD_IMAGENETICS	ss5663575763	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5790554899	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5790554900	Oct 16, 2022 (156)
39	EVA	ss5845949994	Oct 16, 2022 (156)
40	EVA	ss5853218405	Oct 16, 2022 (156)
41	EVA	ss5958508787	Oct 16, 2022 (156)
42	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43736565 (NC_000020.10:62451784::TA 291/3854) Row 43736566 (NC_000020.10:62451784:TA: 1/3854)	-	Oct 12, 2018 (152)
43	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43736565 (NC_000020.10:62451784::TA 291/3854) Row 43736566 (NC_000020.10:62451784:TA: 1/3854)	-	Oct 12, 2018 (152)
44	Genetic variation in the Estonian population	NC_000020.10 - 62451785	Oct 12, 2018 (152)
45	The Danish reference pan genome	NC_000020.10 - 62451785	Apr 27, 2020 (154)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 557055868 (NC_000020.11:63820431::TA 9792/138330) Row 557055869 (NC_000020.11:63820431::TATA 4/138386) Row 557055870 (NC_000020.11:63820431::TATATA 1/138386)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 557055868 (NC_000020.11:63820431::TA 9792/138330) Row 557055869 (NC_000020.11:63820431::TATA 4/138386) Row 557055870 (NC_000020.11:63820431::TATATA 1/138386)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 557055868 (NC_000020.11:63820431::TA 9792/138330) Row 557055869 (NC_000020.11:63820431::TATA 4/138386) Row 557055870 (NC_000020.11:63820431::TATATA 1/138386)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 557055868 (NC_000020.11:63820431::TA 9792/138330) Row 557055869 (NC_000020.11:63820431::TATA 4/138386) Row 557055870 (NC_000020.11:63820431::TATATA 1/138386)...	-	Apr 27, 2021 (155)
50	Genome of the Netherlands Release 5	NC_000020.10 - 62451785	Apr 27, 2020 (154)
51	Northern Sweden	NC_000020.10 - 62451785	Jul 13, 2019 (153)
52	8.3KJPN Submission ignored due to conflicting rows: Row 88454598 (NC_000020.10:62451784::TA 6673/16742) Row 88454599 (NC_000020.10:62451784::TATA 34/16742)	-	Apr 27, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 88454598 (NC_000020.10:62451784::TA 6673/16742) Row 88454599 (NC_000020.10:62451784::TATA 34/16742)	-	Apr 27, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 124392003 (NC_000020.11:63820431::TA 11268/28258) Row 124392004 (NC_000020.11:63820431::TATA 42/28258)	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 124392003 (NC_000020.11:63820431::TA 11268/28258) Row 124392004 (NC_000020.11:63820431::TATA 42/28258)	-	Oct 16, 2022 (156)
56	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43736565 (NC_000020.10:62451784::TA 242/3708) Row 43736566 (NC_000020.10:62451784:TA: 3/3708)	-	Oct 12, 2018 (152)
57	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43736565 (NC_000020.10:62451784::TA 242/3708) Row 43736566 (NC_000020.10:62451784:TA: 3/3708)	-	Oct 12, 2018 (152)
58	ALFA	NC_000020.11 - 63820432	Apr 27, 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)
rs199992473	May 15, 2013 (138)
rs796784735	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1709428620, ss1709428636	NC_000020.10:62451784:TA:	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATAT	(self)
ss3707320650, ss4356509554	NC_000020.11:63820431:TA:	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATAT	(self)
ss327964581, ss552677684, ss553686197, ss1698976423	NC_000020.9:61922228::TA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
ss289421083	NC_000020.9:61922241::AT	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
30904100, 768764, 19476896, 16840340, ss499744736, ss664488982, ss947407452, ss994911749, ss1575739012, ss2031442073, ss3018480894, ss3685165852, ss3743555475, ss3835767037, ss3841508455, ss5230485291, ss5663575763, ss5845949994, ss5958508787	NC_000020.10:62451784::TA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
ss1710822697, ss1710822698	NC_000020.10:62451786::TA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
ss3064005018, ss3847022296, ss4356509550, ss5309449317, ss5501663275, ss5790554899, ss5853218405	NC_000020.11:63820431::TA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
13246295484	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
ss3707320651	NC_000020.11:63820433::TA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
ss80989807	NT_011333.6:1188428::AT	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATAT	(self)
ss5230485292	NC_000020.10:62451784::TATA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATAT	(self)
ss4356509551, ss5309449318, ss5790554900	NC_000020.11:63820431::TATA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATAT	(self)
13246295484	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATAT	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATAT	(self)
ss3707320652	NC_000020.11:63820433::TATA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATAT	(self)
ss4356509552	NC_000020.11:63820431::TATATA	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATATAT	(self)
13246295484	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATATAT	NC_000020.11:63820431:TATATATATATA… NC_000020.11:63820431:TATATATATATAT:TATATATATATATATATAT	(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 rs59953663

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

rs59953663