RGD:150474609 Rat Genome Database

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Variant: RGD:150474609 -  Homo sapiens

RGD ID: 150474609
RS ID: rs4468002
ClinVar ID: CV1202124
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPM6  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 77,354,230
GRCh38 9 74,739,314
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001177310.2:c.5555+53C>T
NM_001177311.2:c.5555+53C>T
NM_017662.5:c.5570+53C>T
NG_017036.1:g.153781C>T
More... 		05/30/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TRPM6
Accession:NM_017662
Location:INTRON

Gene Symbol:TRPM6
Accession:NM_001177310
Location:INTRON

Gene Symbol:TRPM6
Accession:NM_001177311
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001589367 CLINVAR
dbSNP (RS) rs4468002 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TRPM6 CLINVAR
OMIM 607009 CLINVAR