RGD:150410533 Rat Genome Database

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Variant: RGD:150410533 -  Homo sapiens

RGD ID: 150410533
RS ID: rs116807211
ClinVar ID: CV1190047
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SCN11A  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 38,891,713
GRCh38 3 38,850,222
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.11:g.38891713A>G
NM_014139.3:c.4327+259T>C
NG_033859.2:g.206765T>C
NC_000003.12:g.38850222A>G
More... 		12/17/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SCN11A
Accession:NM_014139
Location:INTRON

Gene Symbol:SCN11A
Accession:XM_011533321
Location:INTRON

Gene Symbol:SCN11A
Accession:XM_017005650
Location:INTRON

Gene Symbol:SCN11A
Accession:XM_017005651
Location:INTRON

Gene Symbol:SCN11A
Accession:XM_017005653
Location:INTRON

Gene Symbol:SCN11A
Accession:NM_001349253
Location:INTRON

Gene Symbol:SCN11A
Accession:XM_047447378
Location:INTRON

Gene Symbol:SCN11A
Accession:NR_164473
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001566102 CLINVAR
dbSNP (RS) rs116807211 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SCN11A CLINVAR
OMIM 604385 CLINVAR