Overview

Variant ID 26923
Entrez Gene ID 80036
Gene TRPM3 (GeneCards)
Location hg19 9:73398040-73398040
hg38 9:70783124-70783124
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000009.11:g.73398040 C>G (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 141213431

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.0795
CADD Raw score (version 1.3) -0.013375 (Deleterious)
FATHMM raw prediction score 0.16209 (Tolerated)
Deleterious probability by DeFine 0.4649 (Neutral)
Entrez Gene ID 80036 (NCBI Gene)
Official Gene Symbol TRPM3 (GeneCards)
Number of variants in TRPM3 in this database 15 (view all the variants)
Full name transient receptor potential cation channel subfamily M member 3
Band 9q21.12-q21.13
Other IDs Vega: OTTHUMG00000019997
OMIM: 608961
HGNC: HGNC:17992
Ensembl: ENSG00000083067
Other names GON-2, MLSN2, LTRPC3
Summary The product of this gene belongs to the family of transient receptor potential (TRP) channels. TRP channels are cation-selective channels important for cellular calcium signaling and homeostasis. The protein encoded by this gene mediates calcium entry, and this entry is potentiated by calcium store depletion. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID