RGD:151752278 Rat Genome Database

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Variant: RGD:151752278 -  Homo sapiens

RGD ID: 151752278
RS ID: rs768889606
ClinVar ID: CV1467440
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126862088  TRPM1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 31,318,338
GRCh38 15 31,026,135
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002420.6:c.3563+4C>T
NM_001252024.2:c.3629+4C>T
NM_001252020.2:c.3680+4C>T
NG_016453.2:g.140139C>T
More... 		10/11/2021 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:TRPM1
Accession:NM_001252024
Location:INTRON

Gene Symbol:TRPM1
Accession:NM_002420
Location:INTRON

Gene Symbol:TRPM1
Accession:NM_001252020
Location:INTRON

Gene Symbol:TRPM1
Accession:NM_001252030
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001927638 CLINVAR
dbSNP (RS) rs768889606 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126862088 CLINVAR
  TRPM1 CLINVAR
OMIM 603576 CLINVAR