ClinVar Miner

List of variants in gene TRPC3 studied for hereditary dementia

Included ClinVar conditions (231):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001130698.2(TRPC3):c.117C>T (p.Gly39=) rs1396082 0.41213
NM_001130698.2(TRPC3):c.2285G>A (p.Arg762His) rs142339351 0.00001
NM_001130698.2(TRPC3):c.1419del (p.Val474fs) rs2149125943
NM_001130698.2(TRPC3):c.2216T>C (p.Leu739Pro)
NM_001130698.2(TRPC3):c.2545C>A (p.Gln849Lys)
NM_001130698.2(TRPC3):c.857C>G (p.Ser286Trp)
NM_001130698.2(TRPC3):c.949G>A (p.Glu317Lys) rs2149142103

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