Name: rs747112398
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.

rs747112398

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:66038468-66038482 (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(TC)₃ / delTCTC / delTC / dupTC…
del(TC)₃ / delTCTC / delTC / dupTC / dupTCTC
Variation Type: Indel Insertion and Deletion
Frequency: del(TC)₃=0.00000 (0/11840, ALFA)
delTCTC=0.00000 (0/11840, ALFA)
delTC=0.00000 (0/11840, ALFA) (+ 1 more)
dupTC=0.00000 (0/11840, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: VSIG4 : 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	HWEP
Total	Global	11840	CTCTCTCTCTCTCTC=1.00000	CTCTCTCTC=0.00000, CTCTCTCTCTC=0.00000, CTCTCTCTCTCTC=0.00000, CTCTCTCTCTCTCTCTC=0.00000	1.0	N/A
European	Sub	7610	CTCTCTCTCTCTCTC=1.0000	CTCTCTCTC=0.0000, CTCTCTCTCTC=0.0000, CTCTCTCTCTCTC=0.0000, CTCTCTCTCTCTCTCTC=0.0000	1.0	N/A
African	Sub	2810	CTCTCTCTCTCTCTC=1.0000	CTCTCTCTC=0.0000, CTCTCTCTCTC=0.0000, CTCTCTCTCTCTC=0.0000, CTCTCTCTCTCTCTCTC=0.0000	1.0	N/A
African Others	Sub	108	CTCTCTCTCTCTCTC=1.000	CTCTCTCTC=0.000, CTCTCTCTCTC=0.000, CTCTCTCTCTCTC=0.000, CTCTCTCTCTCTCTCTC=0.000	1.0	N/A
African American	Sub	2702	CTCTCTCTCTCTCTC=1.0000	CTCTCTCTC=0.0000, CTCTCTCTCTC=0.0000, CTCTCTCTCTCTC=0.0000, CTCTCTCTCTCTCTCTC=0.0000	1.0	N/A
Asian	Sub	106	CTCTCTCTCTCTCTC=1.000	CTCTCTCTC=0.000, CTCTCTCTCTC=0.000, CTCTCTCTCTCTC=0.000, CTCTCTCTCTCTCTCTC=0.000	1.0	N/A
East Asian	Sub	84	CTCTCTCTCTCTCTC=1.00	CTCTCTCTC=0.00, CTCTCTCTCTC=0.00, CTCTCTCTCTCTC=0.00, CTCTCTCTCTCTCTCTC=0.00	1.0	N/A
Other Asian	Sub	22	CTCTCTCTCTCTCTC=1.00	CTCTCTCTC=0.00, CTCTCTCTCTC=0.00, CTCTCTCTCTCTC=0.00, CTCTCTCTCTCTCTCTC=0.00	1.0	N/A
Latin American 1	Sub	144	CTCTCTCTCTCTCTC=1.000	CTCTCTCTC=0.000, CTCTCTCTCTC=0.000, CTCTCTCTCTCTC=0.000, CTCTCTCTCTCTCTCTC=0.000	1.0	N/A
Latin American 2	Sub	608	CTCTCTCTCTCTCTC=1.000	CTCTCTCTC=0.000, CTCTCTCTCTC=0.000, CTCTCTCTCTCTC=0.000, CTCTCTCTCTCTCTCTC=0.000	1.0	N/A
South Asian	Sub	92	CTCTCTCTCTCTCTC=1.00	CTCTCTCTC=0.00, CTCTCTCTCTC=0.00, CTCTCTCTCTCTC=0.00, CTCTCTCTCTCTCTCTC=0.00	1.0	N/A
Other	Sub	470	CTCTCTCTCTCTCTC=1.000	CTCTCTCTC=0.000, CTCTCTCTCTC=0.000, CTCTCTCTCTCTC=0.000, CTCTCTCTCTCTCTCTC=0.000	1.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11840	(CT)₇C=1.00000	del(TC)₃=0.00000, delTCTC=0.00000, delTC=0.00000, dupTC=0.00000
Allele Frequency Aggregator	European	Sub	7610	(CT)₇C=1.0000	del(TC)₃=0.0000, delTCTC=0.0000, delTC=0.0000, dupTC=0.0000
Allele Frequency Aggregator	African	Sub	2810	(CT)₇C=1.0000	del(TC)₃=0.0000, delTCTC=0.0000, delTC=0.0000, dupTC=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	608	(CT)₇C=1.000	del(TC)₃=0.000, delTCTC=0.000, delTC=0.000, dupTC=0.000
Allele Frequency Aggregator	Other	Sub	470	(CT)₇C=1.000	del(TC)₃=0.000, delTCTC=0.000, delTC=0.000, dupTC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	(CT)₇C=1.000	del(TC)₃=0.000, delTCTC=0.000, delTC=0.000, dupTC=0.000
Allele Frequency Aggregator	Asian	Sub	106	(CT)₇C=1.000	del(TC)₃=0.000, delTCTC=0.000, delTC=0.000, dupTC=0.000
Allele Frequency Aggregator	South Asian	Sub	92	(CT)₇C=1.00	del(TC)₃=0.00, delTCTC=0.00, delTC=0.00, dupTC=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 X	NC_000023.11:g.66038469TC[4]
GRCh38.p14 chr X	NC_000023.11:g.66038469TC[5]
GRCh38.p14 chr X	NC_000023.11:g.66038469TC[6]
GRCh38.p14 chr X	NC_000023.11:g.66038469TC[8]
GRCh38.p14 chr X	NC_000023.11:g.66038469TC[9]
GRCh37.p13 chr X	NC_000023.10:g.65258311TC[4]
GRCh37.p13 chr X	NC_000023.10:g.65258311TC[5]
GRCh37.p13 chr X	NC_000023.10:g.65258311TC[6]
GRCh37.p13 chr X	NC_000023.10:g.65258311TC[8]
GRCh37.p13 chr X	NC_000023.10:g.65258311TC[9]
VSIG4 RefSeqGene	NG_021306.1:g.6645AG[4]
VSIG4 RefSeqGene	NG_021306.1:g.6645AG[5]
VSIG4 RefSeqGene	NG_021306.1:g.6645AG[6]
VSIG4 RefSeqGene	NG_021306.1:g.6645AG[8]
VSIG4 RefSeqGene	NG_021306.1:g.6645AG[9]

Gene: VSIG4, V-set and immunoglobulin domain containing 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
VSIG4 transcript variant 2	NM_001100431.2:c.55+1463A… NM_001100431.2:c.55+1463AG[4]	N/A	Intron Variant
VSIG4 transcript variant 4	NM_001184830.2:c.55+1463A… NM_001184830.2:c.55+1463AG[4]	N/A	Intron Variant
VSIG4 transcript variant 3	NM_001184831.2:c.55+1463A… NM_001184831.2:c.55+1463AG[4]	N/A	Intron Variant
VSIG4 transcript variant 5	NM_001257403.2:c.55+1463A… NM_001257403.2:c.55+1463AG[4]	N/A	Intron Variant
VSIG4 transcript variant 1	NM_007268.3:c.55+1463AG[4]	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	(CT)₇C=	del(TC)₃	delTCTC	delTC	dupTC	dupTCTC
GRCh38.p14 chr X	NC_000023.11:g.66038468_66038482=	NC_000023.11:g.66038469TC[4]	NC_000023.11:g.66038469TC[5]	NC_000023.11:g.66038469TC[6]	NC_000023.11:g.66038469TC[8]	NC_000023.11:g.66038469TC[9]
GRCh37.p13 chr X	NC_000023.10:g.65258310_65258324=	NC_000023.10:g.65258311TC[4]	NC_000023.10:g.65258311TC[5]	NC_000023.10:g.65258311TC[6]	NC_000023.10:g.65258311TC[8]	NC_000023.10:g.65258311TC[9]
VSIG4 RefSeqGene	NG_021306.1:g.6644_6658=	NG_021306.1:g.6645AG[4]	NG_021306.1:g.6645AG[5]	NG_021306.1:g.6645AG[6]	NG_021306.1:g.6645AG[8]	NG_021306.1:g.6645AG[9]
VSIG4 transcript variant 2	NM_001100431.1:c.55+1476=	NM_001100431.1:c.55+1463AG[4]	NM_001100431.1:c.55+1463AG[5]	NM_001100431.1:c.55+1463AG[6]	NM_001100431.1:c.55+1463AG[8]	NM_001100431.1:c.55+1463AG[9]
VSIG4 transcript variant 2	NM_001100431.2:c.55+1476=	NM_001100431.2:c.55+1463AG[4]	NM_001100431.2:c.55+1463AG[5]	NM_001100431.2:c.55+1463AG[6]	NM_001100431.2:c.55+1463AG[8]	NM_001100431.2:c.55+1463AG[9]
VSIG4 transcript variant 4	NM_001184830.1:c.55+1476=	NM_001184830.1:c.55+1463AG[4]	NM_001184830.1:c.55+1463AG[5]	NM_001184830.1:c.55+1463AG[6]	NM_001184830.1:c.55+1463AG[8]	NM_001184830.1:c.55+1463AG[9]
VSIG4 transcript variant 4	NM_001184830.2:c.55+1476=	NM_001184830.2:c.55+1463AG[4]	NM_001184830.2:c.55+1463AG[5]	NM_001184830.2:c.55+1463AG[6]	NM_001184830.2:c.55+1463AG[8]	NM_001184830.2:c.55+1463AG[9]
VSIG4 transcript variant 3	NM_001184831.1:c.55+1476=	NM_001184831.1:c.55+1463AG[4]	NM_001184831.1:c.55+1463AG[5]	NM_001184831.1:c.55+1463AG[6]	NM_001184831.1:c.55+1463AG[8]	NM_001184831.1:c.55+1463AG[9]
VSIG4 transcript variant 3	NM_001184831.2:c.55+1476=	NM_001184831.2:c.55+1463AG[4]	NM_001184831.2:c.55+1463AG[5]	NM_001184831.2:c.55+1463AG[6]	NM_001184831.2:c.55+1463AG[8]	NM_001184831.2:c.55+1463AG[9]
VSIG4 transcript variant 5	NM_001257403.1:c.55+1476=	NM_001257403.1:c.55+1463AG[4]	NM_001257403.1:c.55+1463AG[5]	NM_001257403.1:c.55+1463AG[6]	NM_001257403.1:c.55+1463AG[8]	NM_001257403.1:c.55+1463AG[9]
VSIG4 transcript variant 5	NM_001257403.2:c.55+1476=	NM_001257403.2:c.55+1463AG[4]	NM_001257403.2:c.55+1463AG[5]	NM_001257403.2:c.55+1463AG[6]	NM_001257403.2:c.55+1463AG[8]	NM_001257403.2:c.55+1463AG[9]
VSIG4 transcript variant 1	NM_007268.2:c.55+1476=	NM_007268.2:c.55+1463AG[4]	NM_007268.2:c.55+1463AG[5]	NM_007268.2:c.55+1463AG[6]	NM_007268.2:c.55+1463AG[8]	NM_007268.2:c.55+1463AG[9]
VSIG4 transcript variant 1	NM_007268.3:c.55+1476=	NM_007268.3:c.55+1463AG[4]	NM_007268.3:c.55+1463AG[5]	NM_007268.3:c.55+1463AG[6]	NM_007268.3:c.55+1463AG[8]	NM_007268.3:c.55+1463AG[9]
VSIG4 transcript variant X1	XM_005262240.1:c.55+1476=	XM_005262240.1:c.55+1463AG[4]	XM_005262240.1:c.55+1463AG[5]	XM_005262240.1:c.55+1463AG[6]	XM_005262240.1:c.55+1463AG[8]	XM_005262240.1:c.55+1463AG[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#.

20 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_UK10K_ALSPAC	ss1709743891	Apr 01, 2015 (144)
2	EVA_UK10K_TWINSUK	ss1709743937	Apr 01, 2015 (144)
3	EVA_UK10K_ALSPAC	ss1710863957	Apr 01, 2015 (144)
4	EVA_UK10K_TWINSUK	ss1710864004	Apr 01, 2015 (144)
5	SWEGEN	ss3020073084	Nov 08, 2017 (151)
6	GNOMAD	ss4372752263	Apr 27, 2021 (155)
7	GNOMAD	ss4372752264	Apr 27, 2021 (155)
8	GNOMAD	ss4372752265	Apr 27, 2021 (155)
9	GNOMAD	ss4372752266	Apr 27, 2021 (155)
10	GNOMAD	ss4372752267	Apr 27, 2021 (155)
11	TOPMED	ss5125037976	Apr 27, 2021 (155)
12	TOPMED	ss5125037977	Apr 27, 2021 (155)
13	TOMMO_GENOMICS	ss5234734203	Apr 27, 2021 (155)
14	TOMMO_GENOMICS	ss5234734204	Apr 27, 2021 (155)
15	TOMMO_GENOMICS	ss5234734205	Apr 27, 2021 (155)
16	1000G_HIGH_COVERAGE	ss5312736221	Oct 17, 2022 (156)
17	HUGCELL_USP	ss5504359629	Oct 17, 2022 (156)
18	TOMMO_GENOMICS	ss5796639891	Oct 17, 2022 (156)
19	TOMMO_GENOMICS	ss5796639892	Oct 17, 2022 (156)
20	TOMMO_GENOMICS	ss5796639893	Oct 17, 2022 (156)
21	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 45614431 (NC_000023.10:65258309:CT: 120/2889) Row 45614432 (NC_000023.10:65258309::CT 17/2889)	-	Oct 12, 2018 (152)
22	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 45614431 (NC_000023.10:65258309:CT: 120/2889) Row 45614432 (NC_000023.10:65258309::CT 17/2889)	-	Oct 12, 2018 (152)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 582322713 (NC_000023.11:66038467::CT 66/86571) Row 582322714 (NC_000023.11:66038467::CTCT 1/86572) Row 582322715 (NC_000023.11:66038467:CT: 78/86521)...	-	Apr 27, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 582322713 (NC_000023.11:66038467::CT 66/86571) Row 582322714 (NC_000023.11:66038467::CTCT 1/86572) Row 582322715 (NC_000023.11:66038467:CT: 78/86521)...	-	Apr 27, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 582322713 (NC_000023.11:66038467::CT 66/86571) Row 582322714 (NC_000023.11:66038467::CTCT 1/86572) Row 582322715 (NC_000023.11:66038467:CT: 78/86521)...	-	Apr 27, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 582322713 (NC_000023.11:66038467::CT 66/86571) Row 582322714 (NC_000023.11:66038467::CTCT 1/86572) Row 582322715 (NC_000023.11:66038467:CT: 78/86521)...	-	Apr 27, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 582322713 (NC_000023.11:66038467::CT 66/86571) Row 582322714 (NC_000023.11:66038467::CTCT 1/86572) Row 582322715 (NC_000023.11:66038467:CT: 78/86521)...	-	Apr 27, 2021 (155)
28	8.3KJPN Submission ignored due to conflicting rows: Row 92703510 (NC_000023.10:65258309::CT 7/12832) Row 92703511 (NC_000023.10:65258309:CT: 3/12832) Row 92703512 (NC_000023.10:65258309:CTCT: 1/12832)	-	Apr 27, 2021 (155)
29	8.3KJPN Submission ignored due to conflicting rows: Row 92703510 (NC_000023.10:65258309::CT 7/12832) Row 92703511 (NC_000023.10:65258309:CT: 3/12832) Row 92703512 (NC_000023.10:65258309:CTCT: 1/12832)	-	Apr 27, 2021 (155)
30	8.3KJPN Submission ignored due to conflicting rows: Row 92703510 (NC_000023.10:65258309::CT 7/12832) Row 92703511 (NC_000023.10:65258309:CT: 3/12832) Row 92703512 (NC_000023.10:65258309:CTCT: 1/12832)	-	Apr 27, 2021 (155)
31	14KJPN Submission ignored due to conflicting rows: Row 130476995 (NC_000023.11:66038467::CT 13/22223) Row 130476996 (NC_000023.11:66038467:CT: 2/22223) Row 130476997 (NC_000023.11:66038467:CTCT: 1/22223)	-	Oct 17, 2022 (156)
32	14KJPN Submission ignored due to conflicting rows: Row 130476995 (NC_000023.11:66038467::CT 13/22223) Row 130476996 (NC_000023.11:66038467:CT: 2/22223) Row 130476997 (NC_000023.11:66038467:CTCT: 1/22223)	-	Oct 17, 2022 (156)
33	14KJPN Submission ignored due to conflicting rows: Row 130476995 (NC_000023.11:66038467::CT 13/22223) Row 130476996 (NC_000023.11:66038467:CT: 2/22223) Row 130476997 (NC_000023.11:66038467:CTCT: 1/22223)	-	Oct 17, 2022 (156)
34	TopMed Submission ignored due to conflicting rows: Row 688644333 (NC_000023.11:66038467:CTCT: 3/264690) Row 688644334 (NC_000023.11:66038467:CTCTCT: 6/264690)	-	Apr 27, 2021 (155)
35	TopMed Submission ignored due to conflicting rows: Row 688644333 (NC_000023.11:66038467:CTCT: 3/264690) Row 688644334 (NC_000023.11:66038467:CTCTCT: 6/264690)	-	Apr 27, 2021 (155)
36	UK 10K study - Twins Submission ignored due to conflicting rows: Row 45614431 (NC_000023.10:65258309:CT: 165/3708) Row 45614432 (NC_000023.10:65258309::CT 22/3708)	-	Oct 12, 2018 (152)
37	UK 10K study - Twins Submission ignored due to conflicting rows: Row 45614431 (NC_000023.10:65258309:CT: 165/3708) Row 45614432 (NC_000023.10:65258309::CT 22/3708)	-	Oct 12, 2018 (152)
38	ALFA	NC_000023.11 - 66038468	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4372752267, ss5125037977	NC_000023.11:66038467:CTCTCT:	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTC	(self)
13697368423	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTC	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTC	(self)
ss5234734205	NC_000023.10:65258309:CTCT:	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTC	(self)
ss4372752266, ss5125037976, ss5796639893	NC_000023.11:66038467:CTCT:	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTC	(self)
13697368423	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTC	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTC	(self)
ss1709743891, ss1709743937, ss3020073084, ss5234734204	NC_000023.10:65258309:CT:	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTC	(self)
ss4372752265, ss5796639892	NC_000023.11:66038467:CT:	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTC	(self)
13697368423	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTC	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTC	(self)
ss5234734203	NC_000023.10:65258309::CT	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTC	(self)
ss1710863957, ss1710864004	NC_000023.10:65258311::CT	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTC	(self)
ss4372752263, ss5312736221, ss5504359629, ss5796639891	NC_000023.11:66038467::CT	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTC	(self)
13697368423	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTC	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTC	(self)
ss4372752264	NC_000023.11:66038467::CTCT	NC_000023.11:66038467:CTCTCTCTCTCT… NC_000023.11:66038467:CTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTC	(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 rs747112398

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

rs747112398