RGD:12906072 Rat Genome Database

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Variant: RGD:12906072 -  Homo sapiens

RGD ID: 12906072
RS ID: rs1064797293
ClinVar ID: CV413624
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SCN10A  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 38,830,439
GRCh38 3 38,788,948
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_031891.2:g.10063G>A
NC_000003.12:g.38788948C>T
NC_000003.11:g.38830439C>T
NM_001293306.2:c.470+8G>A
More... 		01/31/2017 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:SCN10A
Accession:XM_005265371
Location:INTRON

Gene Symbol:SCN10A
Accession:XM_011533993
Location:INTRON

Gene Symbol:SCN10A
Accession:NM_006514
Location:INTRON

Gene Symbol:SCN10A
Accession:XM_011533994
Location:INTRON

Gene Symbol:SCN10A
Accession:NM_001293307
Location:INTRON

Gene Symbol:SCN10A
Accession:NM_001293306
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000488382 CLINVAR
dbSNP (RS) rs1064797293 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SCN10A CLINVAR
OMIM 604427 CLINVAR