RGD:8651289 Rat Genome Database

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Variant: RGD:8651289 -  Homo sapiens

RGD ID: 8651289
ClinVar ID: CV127864
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPM3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 73,533,345
GRCh38 9 70,918,429
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.70918429C>T
NC_000009.11:g.73533345C>T
NM_001007471.2:c.178-53918G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:TRPM3
Accession:NM_001007471
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_206948
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366153
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_020952
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366145
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366142
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366146
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366149
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366148
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366154
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366147
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366143
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366144
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_206946
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001007470
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_206944
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_206945
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_024971
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366141
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366150
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366151
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_001366152
Location:INTRON

Gene Symbol:TRPM3
Accession:NM_206947
Location:INTRON

Variant Samples