RGD:12846687 Rat Genome Database

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Variant: RGD:12846687 -  Homo sapiens

RGD ID: 12846687
RS ID: rs1057523824
ClinVar ID: CV367562
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SCN10A  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 38,830,542
GRCh38 3 38,789,051
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.9960A>G
NC_000003.12:g.38789051T>C
NC_000003.11:g.38830542T>C
NM_006514.2:c.390-15A>G
More... 		11/07/2016 intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:SCN10A
Accession:NM_006514
Location:INTRON

Gene Symbol:SCN10A
Accession:XM_005265371
Location:INTRON

Gene Symbol:SCN10A
Accession:XM_011533993
Location:INTRON

Gene Symbol:SCN10A
Accession:NM_001293307
Location:INTRON

Gene Symbol:SCN10A
Accession:NM_001293306
Location:INTRON

Gene Symbol:SCN10A
Accession:XM_011533994
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000442116 CLINVAR
dbSNP (RS) rs1057523824 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene SCN10A CLINVAR
OMIM 604427 CLINVAR