RGD:155800853 Rat Genome Database

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Variant: RGD:155800853 -  Homo sapiens

RGD ID: 155800853
ClinVar ID: CV1863848
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SCN1A-AS1  SCN9A  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 167,060,984
GRCh38 2 166,204,474
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001365536.1:c.4399-10G>C
LRG_369:g.176514G>C
NC_000002.11:g.167060984C>G
NC_000002.12:g.166204474C>G
More... 		03/22/2022 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:SCN9A
Accession:NM_002977
Location:INTRON

Gene Symbol:SCN9A
Accession:XM_011511618
Location:INTRON

Gene Symbol:SCN9A
Accession:XM_011511617
Location:INTRON

Gene Symbol:SCN9A
Accession:XM_011511616
Location:INTRON

Gene Symbol:SCN9A
Accession:XM_011511619
Location:INTRON

Gene Symbol:SCN9A
Accession:XM_017004669
Location:INTRON

Gene Symbol:SCN9A
Accession:NM_001365536
Location:INTRON

Gene Symbol:SCN9A
Accession:XR_001738886
Location:INTRON;NON-CODING

Gene Symbol:SCN1A-AS1
Accession:NR_110260
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:26467025  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002474271 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SCN1A-AS1 CLINVAR
  SCN9A CLINVAR
OMIM 603415 CLINVAR