Name: rs1491449720
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.

rs1491449720

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:120347147-120347148 (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: insTTT / insTTTCT / insTTTCTTT / i…
insTTT / insTTTCT / insTTTCTTT / ins(TTTC)₂TTT / ins(TTTC)₃TTT / ins(TTTC)₄TTT
Variation Type: Insertion
Frequency: None

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ARHGEF12 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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").

None

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 11	NC_000011.10:g.120347147_120347148insTTT
GRCh38.p14 chr 11	NC_000011.10:g.120347147_120347148insTTTCT
GRCh38.p14 chr 11	NC_000011.10:g.120347147_120347148insTTTCTTT
GRCh38.p14 chr 11	NC_000011.10:g.120347147_120347148insTTTCTTTCTTT
GRCh38.p14 chr 11	NC_000011.10:g.120347147_120347148insTTTCTTTCTTTCTTT
GRCh38.p14 chr 11	NC_000011.10:g.120347147_120347148insTTTCTTTCTTTCTTTCTTT
GRCh37.p13 chr 11	NC_000011.9:g.120217856_120217857insTTT
GRCh37.p13 chr 11	NC_000011.9:g.120217856_120217857insTTTCT
GRCh37.p13 chr 11	NC_000011.9:g.120217856_120217857insTTTCTTT
GRCh37.p13 chr 11	NC_000011.9:g.120217856_120217857insTTTCTTTCTTT
GRCh37.p13 chr 11	NC_000011.9:g.120217856_120217857insTTTCTTTCTTTCTTT
GRCh37.p13 chr 11	NC_000011.9:g.120217856_120217857insTTTCTTTCTTTCTTTCTTT
ARHGEF12 RefSeqGene	NG_027960.1:g.15239_15240insTTT
ARHGEF12 RefSeqGene	NG_027960.1:g.15239_15240insTTTCT
ARHGEF12 RefSeqGene	NG_027960.1:g.15239_15240insTTTCTTT
ARHGEF12 RefSeqGene	NG_027960.1:g.15239_15240insTTTCTTTCTTT
ARHGEF12 RefSeqGene	NG_027960.1:g.15239_15240insTTTCTTTCTTTCTTT
ARHGEF12 RefSeqGene	NG_027960.1:g.15239_15240insTTTCTTTCTTTCTTTCTTT

Gene: ARHGEF12, Rho guanine nucleotide exchange factor 12 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ARHGEF12 transcript variant 2	NM_001198665.2:c.32+9872_… NM_001198665.2:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant 1	NM_015313.3:c.32+9872_32+… NM_015313.3:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant 3	NM_001301084.2:c.	N/A	Genic Upstream Transcript Variant
ARHGEF12 transcript variant X1	XM_006718805.4:c.32+9872_… XM_006718805.4:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X6	XM_011542720.3:c.-278+104… XM_011542720.3:c.-278+10471_-278+10472insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X4	XM_017017420.2:c.32+9872_… XM_017017420.2:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X10	XM_017017421.2:c.-278+927… XM_017017421.2:c.-278+9278_-278+9279insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X2	XM_047426659.1:c.32+9872_… XM_047426659.1:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X3	XM_047426660.1:c.32+9872_… XM_047426660.1:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X5	XM_047426661.1:c.32+9872_… XM_047426661.1:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X7	XM_047426662.1:c.32+9872_… XM_047426662.1:c.32+9872_32+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X8	XM_047426663.1:c.-221+104… XM_047426663.1:c.-221+10471_-221+10472insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X11	XM_047426665.1:c.-111+987… XM_047426665.1:c.-111+9872_-111+9873insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X12	XM_047426666.1:c.-278+104… XM_047426666.1:c.-278+10471_-278+10472insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X13	XM_047426667.1:c.-221+104… XM_047426667.1:c.-221+10471_-221+10472insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X14	XM_047426668.1:c.-221+104… XM_047426668.1:c.-221+10471_-221+10472insTTT	N/A	Intron Variant
ARHGEF12 transcript variant X9	XM_047426664.1:c.	N/A	Genic Upstream Transcript Variant
ARHGEF12 transcript variant X15	XM_047426669.1:c.	N/A	Genic Upstream Transcript Variant
ARHGEF12 transcript variant X16	XM_047426670.1:c.	N/A	Genic Upstream Transcript 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	=	insTTT	insTTTCT	insTTTCTTT	ins(TTTC)₂TTT	ins(TTTC)₃TTT	ins(TTTC)₄TTT
GRCh38.p14 chr 11	NC_000011.10:g.120347147_120347148=	NC_000011.10:g.120347147_120347148insTTT	NC_000011.10:g.120347147_120347148insTTTCT	NC_000011.10:g.120347147_120347148insTTTCTTT	NC_000011.10:g.120347147_120347148insTTTCTTTCTTT	NC_000011.10:g.120347147_120347148insTTTCTTTCTTTCTTT	NC_000011.10:g.120347147_120347148insTTTCTTTCTTTCTTTCTTT
GRCh37.p13 chr 11	NC_000011.9:g.120217856_120217857=	NC_000011.9:g.120217856_120217857insTTT	NC_000011.9:g.120217856_120217857insTTTCT	NC_000011.9:g.120217856_120217857insTTTCTTT	NC_000011.9:g.120217856_120217857insTTTCTTTCTTT	NC_000011.9:g.120217856_120217857insTTTCTTTCTTTCTTT	NC_000011.9:g.120217856_120217857insTTTCTTTCTTTCTTTCTTT
ARHGEF12 RefSeqGene	NG_027960.1:g.15239_15240=	NG_027960.1:g.15239_15240insTTT	NG_027960.1:g.15239_15240insTTTCT	NG_027960.1:g.15239_15240insTTTCTTT	NG_027960.1:g.15239_15240insTTTCTTTCTTT	NG_027960.1:g.15239_15240insTTTCTTTCTTTCTTT	NG_027960.1:g.15239_15240insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant 2	NM_001198665.1:c.32+9873=	NM_001198665.1:c.32+9872_32+9873insTTT	NM_001198665.1:c.32+9872_32+9873insTTTCT	NM_001198665.1:c.32+9872_32+9873insTTTCTTT	NM_001198665.1:c.32+9872_32+9873insTTTCTTTCTTT	NM_001198665.1:c.32+9872_32+9873insTTTCTTTCTTTCTTT	NM_001198665.1:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant 2	NM_001198665.2:c.32+9873=	NM_001198665.2:c.32+9872_32+9873insTTT	NM_001198665.2:c.32+9872_32+9873insTTTCT	NM_001198665.2:c.32+9872_32+9873insTTTCTTT	NM_001198665.2:c.32+9872_32+9873insTTTCTTTCTTT	NM_001198665.2:c.32+9872_32+9873insTTTCTTTCTTTCTTT	NM_001198665.2:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant 1	NM_015313.2:c.32+9873=	NM_015313.2:c.32+9872_32+9873insTTT	NM_015313.2:c.32+9872_32+9873insTTTCT	NM_015313.2:c.32+9872_32+9873insTTTCTTT	NM_015313.2:c.32+9872_32+9873insTTTCTTTCTTT	NM_015313.2:c.32+9872_32+9873insTTTCTTTCTTTCTTT	NM_015313.2:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant 1	NM_015313.3:c.32+9873=	NM_015313.3:c.32+9872_32+9873insTTT	NM_015313.3:c.32+9872_32+9873insTTTCT	NM_015313.3:c.32+9872_32+9873insTTTCTTT	NM_015313.3:c.32+9872_32+9873insTTTCTTTCTTT	NM_015313.3:c.32+9872_32+9873insTTTCTTTCTTTCTTT	NM_015313.3:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X1	XM_005271478.1:c.32+9873=	XM_005271478.1:c.32+9872_32+9873insTTT	XM_005271478.1:c.32+9872_32+9873insTTTCT	XM_005271478.1:c.32+9872_32+9873insTTTCTTT	XM_005271478.1:c.32+9872_32+9873insTTTCTTTCTTT	XM_005271478.1:c.32+9872_32+9873insTTTCTTTCTTTCTTT	XM_005271478.1:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X3	XM_005271480.1:c.-278+9279=	XM_005271480.1:c.-278+9278_-278+9279insTTT	XM_005271480.1:c.-278+9278_-278+9279insTTTCT	XM_005271480.1:c.-278+9278_-278+9279insTTTCTTT	XM_005271480.1:c.-278+9278_-278+9279insTTTCTTTCTTT	XM_005271480.1:c.-278+9278_-278+9279insTTTCTTTCTTTCTTT	XM_005271480.1:c.-278+9278_-278+9279insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X1	XM_006718805.4:c.32+9873=	XM_006718805.4:c.32+9872_32+9873insTTT	XM_006718805.4:c.32+9872_32+9873insTTTCT	XM_006718805.4:c.32+9872_32+9873insTTTCTTT	XM_006718805.4:c.32+9872_32+9873insTTTCTTTCTTT	XM_006718805.4:c.32+9872_32+9873insTTTCTTTCTTTCTTT	XM_006718805.4:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X6	XM_011542720.3:c.-278+10472=	XM_011542720.3:c.-278+10471_-278+10472insTTT	XM_011542720.3:c.-278+10471_-278+10472insTTTCT	XM_011542720.3:c.-278+10471_-278+10472insTTTCTTT	XM_011542720.3:c.-278+10471_-278+10472insTTTCTTTCTTT	XM_011542720.3:c.-278+10471_-278+10472insTTTCTTTCTTTCTTT	XM_011542720.3:c.-278+10471_-278+10472insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X4	XM_017017420.2:c.32+9873=	XM_017017420.2:c.32+9872_32+9873insTTT	XM_017017420.2:c.32+9872_32+9873insTTTCT	XM_017017420.2:c.32+9872_32+9873insTTTCTTT	XM_017017420.2:c.32+9872_32+9873insTTTCTTTCTTT	XM_017017420.2:c.32+9872_32+9873insTTTCTTTCTTTCTTT	XM_017017420.2:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X10	XM_017017421.2:c.-278+9279=	XM_017017421.2:c.-278+9278_-278+9279insTTT	XM_017017421.2:c.-278+9278_-278+9279insTTTCT	XM_017017421.2:c.-278+9278_-278+9279insTTTCTTT	XM_017017421.2:c.-278+9278_-278+9279insTTTCTTTCTTT	XM_017017421.2:c.-278+9278_-278+9279insTTTCTTTCTTTCTTT	XM_017017421.2:c.-278+9278_-278+9279insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X2	XM_047426659.1:c.32+9873=	XM_047426659.1:c.32+9872_32+9873insTTT	XM_047426659.1:c.32+9872_32+9873insTTTCT	XM_047426659.1:c.32+9872_32+9873insTTTCTTT	XM_047426659.1:c.32+9872_32+9873insTTTCTTTCTTT	XM_047426659.1:c.32+9872_32+9873insTTTCTTTCTTTCTTT	XM_047426659.1:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X3	XM_047426660.1:c.32+9873=	XM_047426660.1:c.32+9872_32+9873insTTT	XM_047426660.1:c.32+9872_32+9873insTTTCT	XM_047426660.1:c.32+9872_32+9873insTTTCTTT	XM_047426660.1:c.32+9872_32+9873insTTTCTTTCTTT	XM_047426660.1:c.32+9872_32+9873insTTTCTTTCTTTCTTT	XM_047426660.1:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X5	XM_047426661.1:c.32+9873=	XM_047426661.1:c.32+9872_32+9873insTTT	XM_047426661.1:c.32+9872_32+9873insTTTCT	XM_047426661.1:c.32+9872_32+9873insTTTCTTT	XM_047426661.1:c.32+9872_32+9873insTTTCTTTCTTT	XM_047426661.1:c.32+9872_32+9873insTTTCTTTCTTTCTTT	XM_047426661.1:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X7	XM_047426662.1:c.32+9873=	XM_047426662.1:c.32+9872_32+9873insTTT	XM_047426662.1:c.32+9872_32+9873insTTTCT	XM_047426662.1:c.32+9872_32+9873insTTTCTTT	XM_047426662.1:c.32+9872_32+9873insTTTCTTTCTTT	XM_047426662.1:c.32+9872_32+9873insTTTCTTTCTTTCTTT	XM_047426662.1:c.32+9872_32+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X8	XM_047426663.1:c.-221+10472=	XM_047426663.1:c.-221+10471_-221+10472insTTT	XM_047426663.1:c.-221+10471_-221+10472insTTTCT	XM_047426663.1:c.-221+10471_-221+10472insTTTCTTT	XM_047426663.1:c.-221+10471_-221+10472insTTTCTTTCTTT	XM_047426663.1:c.-221+10471_-221+10472insTTTCTTTCTTTCTTT	XM_047426663.1:c.-221+10471_-221+10472insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X11	XM_047426665.1:c.-111+9873=	XM_047426665.1:c.-111+9872_-111+9873insTTT	XM_047426665.1:c.-111+9872_-111+9873insTTTCT	XM_047426665.1:c.-111+9872_-111+9873insTTTCTTT	XM_047426665.1:c.-111+9872_-111+9873insTTTCTTTCTTT	XM_047426665.1:c.-111+9872_-111+9873insTTTCTTTCTTTCTTT	XM_047426665.1:c.-111+9872_-111+9873insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X12	XM_047426666.1:c.-278+10472=	XM_047426666.1:c.-278+10471_-278+10472insTTT	XM_047426666.1:c.-278+10471_-278+10472insTTTCT	XM_047426666.1:c.-278+10471_-278+10472insTTTCTTT	XM_047426666.1:c.-278+10471_-278+10472insTTTCTTTCTTT	XM_047426666.1:c.-278+10471_-278+10472insTTTCTTTCTTTCTTT	XM_047426666.1:c.-278+10471_-278+10472insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X13	XM_047426667.1:c.-221+10472=	XM_047426667.1:c.-221+10471_-221+10472insTTT	XM_047426667.1:c.-221+10471_-221+10472insTTTCT	XM_047426667.1:c.-221+10471_-221+10472insTTTCTTT	XM_047426667.1:c.-221+10471_-221+10472insTTTCTTTCTTT	XM_047426667.1:c.-221+10471_-221+10472insTTTCTTTCTTTCTTT	XM_047426667.1:c.-221+10471_-221+10472insTTTCTTTCTTTCTTTCTTT
ARHGEF12 transcript variant X14	XM_047426668.1:c.-221+10472=	XM_047426668.1:c.-221+10471_-221+10472insTTT	XM_047426668.1:c.-221+10471_-221+10472insTTTCT	XM_047426668.1:c.-221+10471_-221+10472insTTTCTTT	XM_047426668.1:c.-221+10471_-221+10472insTTTCTTTCTTT	XM_047426668.1:c.-221+10471_-221+10472insTTTCTTTCTTTCTTT	XM_047426668.1:c.-221+10471_-221+10472insTTTCTTTCTTTCTTTCTTT

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#.

14 SubSNP, 9 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	MCHAISSO	ss3064537569	Jan 10, 2018 (151)
2	ACPOP	ss3738596443	Jul 13, 2019 (153)
3	ACPOP	ss3738596444	Jul 13, 2019 (153)
4	ACPOP	ss3738596445	Jul 13, 2019 (153)
5	GNOMAD	ss4243716625	Apr 26, 2021 (155)
6	GNOMAD	ss4243716626	Apr 26, 2021 (155)
7	GNOMAD	ss4243716627	Apr 26, 2021 (155)
8	GNOMAD	ss4243716628	Apr 26, 2021 (155)
9	GNOMAD	ss4243716629	Apr 26, 2021 (155)
10	GNOMAD	ss4243716630	Apr 26, 2021 (155)
11	HUGCELL_USP	ss5484093660	Oct 16, 2022 (156)
12	HUGCELL_USP	ss5484093661	Oct 16, 2022 (156)
13	HUGCELL_USP	ss5484093662	Oct 16, 2022 (156)
14	HUGCELL_USP	ss5484093663	Oct 16, 2022 (156)
15	gnomAD - Genomes Submission ignored due to conflicting rows: Row 393831391 (NC_000011.10:120347147::TTT 4354/42808) Row 393831392 (NC_000011.10:120347147::TTTCT 3/43020) Row 393831393 (NC_000011.10:120347147::TTTCTTT 790/42856)...	-	Apr 26, 2021 (155)
16	gnomAD - Genomes Submission ignored due to conflicting rows: Row 393831391 (NC_000011.10:120347147::TTT 4354/42808) Row 393831392 (NC_000011.10:120347147::TTTCT 3/43020) Row 393831393 (NC_000011.10:120347147::TTTCTTT 790/42856)...	-	Apr 26, 2021 (155)
17	gnomAD - Genomes Submission ignored due to conflicting rows: Row 393831391 (NC_000011.10:120347147::TTT 4354/42808) Row 393831392 (NC_000011.10:120347147::TTTCT 3/43020) Row 393831393 (NC_000011.10:120347147::TTTCTTT 790/42856)...	-	Apr 26, 2021 (155)
18	gnomAD - Genomes Submission ignored due to conflicting rows: Row 393831391 (NC_000011.10:120347147::TTT 4354/42808) Row 393831392 (NC_000011.10:120347147::TTTCT 3/43020) Row 393831393 (NC_000011.10:120347147::TTTCTTT 790/42856)...	-	Apr 26, 2021 (155)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 393831391 (NC_000011.10:120347147::TTT 4354/42808) Row 393831392 (NC_000011.10:120347147::TTTCT 3/43020) Row 393831393 (NC_000011.10:120347147::TTTCTTT 790/42856)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 393831391 (NC_000011.10:120347147::TTT 4354/42808) Row 393831392 (NC_000011.10:120347147::TTTCT 3/43020) Row 393831393 (NC_000011.10:120347147::TTTCTTT 790/42856)...	-	Apr 26, 2021 (155)
21	Northern Sweden Submission ignored due to conflicting rows: Row 11881308 (NC_000011.9:120217856:: 531/584, NC_000011.9:120217856::TTT 53/584) Row 11881309 (NC_000011.9:120217856:: 579/584, NC_000011.9:120217856::TTTCTTT 5/584) Row 11881310 (NC_000011.9:120217856:: 583/584, NC_000011.9:120217856::TTTCTTTCTTT 1/584)	-	Jul 13, 2019 (153)
22	Northern Sweden Submission ignored due to conflicting rows: Row 11881308 (NC_000011.9:120217856:: 531/584, NC_000011.9:120217856::TTT 53/584) Row 11881309 (NC_000011.9:120217856:: 579/584, NC_000011.9:120217856::TTTCTTT 5/584) Row 11881310 (NC_000011.9:120217856:: 583/584, NC_000011.9:120217856::TTTCTTTCTTT 1/584)	-	Jul 13, 2019 (153)
23	Northern Sweden Submission ignored due to conflicting rows: Row 11881308 (NC_000011.9:120217856:: 531/584, NC_000011.9:120217856::TTT 53/584) Row 11881309 (NC_000011.9:120217856:: 579/584, NC_000011.9:120217856::TTTCTTT 5/584) Row 11881310 (NC_000011.9:120217856:: 583/584, NC_000011.9:120217856::TTTCTTTCTTT 1/584)	-	Jul 13, 2019 (153)

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
ss3738596443	NC_000011.9:120217856::TTT	NC_000011.10:120347147::TTT	(self)
ss4243716625, ss5484093660	NC_000011.10:120347147::TTT	NC_000011.10:120347147::TTT	(self)
ss4243716626	NC_000011.10:120347147::TTTCT	NC_000011.10:120347147::TTTCT	(self)
ss3738596444	NC_000011.9:120217856::TTTCTTT	NC_000011.10:120347147::TTTCTTT	(self)
ss3064537569, ss4243716627, ss5484093661	NC_000011.10:120347147::TTTCTTT	NC_000011.10:120347147::TTTCTTT	(self)
ss3738596445	NC_000011.9:120217856::TTTCTTTCTTT	NC_000011.10:120347147::TTTCTTTCTTT	(self)
ss4243716628, ss5484093662	NC_000011.10:120347147::TTTCTTTCTTT	NC_000011.10:120347147::TTTCTTTCTTT	(self)
ss4243716629, ss5484093663	NC_000011.10:120347147::TTTCTTTCTT… NC_000011.10:120347147::TTTCTTTCTTTCTTT	NC_000011.10:120347147::TTTCTTTCTT… NC_000011.10:120347147::TTTCTTTCTTTCTTT	(self)
ss4243716630	NC_000011.10:120347147::TTTCTTTCTT… NC_000011.10:120347147::TTTCTTTCTTTCTTTCTTT	NC_000011.10:120347147::TTTCTTTCTT… NC_000011.10:120347147::TTTCTTTCTTTCTTTCTTT	(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 rs1491449720

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

rs1491449720