RGD:15165194 Rat Genome Database

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Variant: RGD:15165194 -  Homo sapiens

RGD ID: 15165194
RS ID: rs114046227
ClinVar ID: CV779925
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPV1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 3,495,352
GRCh38 17 3,592,058
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018727.5:c.284+9G>A
NM_080704.4:c.284+9G>A
NM_080705.4:c.284+9G>A
NM_080706.3:c.284+9G>A
More... 		04/03/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TRPV1
Accession:NM_018727
Location:INTRON

Gene Symbol:TRPV1
Accession:NM_080704
Location:INTRON

Gene Symbol:TRPV1
Accession:NM_080706
Location:INTRON

Gene Symbol:TRPV1
Accession:NM_080705
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000970898 CLINVAR
dbSNP (RS) rs114046227 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TRPV1 CLINVAR
OMIM 602076 CLINVAR