ClinVar Miner

List of variants in gene TRPC6 studied for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP
NM_004621.5(TRPC6):c.*1020G>A rs201292926
NM_004621.5(TRPC6):c.*1038T>G rs142655335
NM_004621.5(TRPC6):c.*1089C>T rs117895343
NM_004621.5(TRPC6):c.*1176T>C rs886047535
NM_004621.5(TRPC6):c.*1349T>C rs180930016
NM_004621.5(TRPC6):c.*1380G>A rs747229991
NM_004621.5(TRPC6):c.*13C>T rs200791047
NM_004621.5(TRPC6):c.*175A>C rs199878670
NM_004621.5(TRPC6):c.*314C>G rs199583740
NM_004621.5(TRPC6):c.*336C>T rs199619303
NM_004621.5(TRPC6):c.*337G>A rs144714163
NM_004621.5(TRPC6):c.*33delT rs753955901
NM_004621.5(TRPC6):c.*40T>G rs201285907
NM_004621.5(TRPC6):c.*509_*512dupCTTA rs557577176
NM_004621.5(TRPC6):c.*530T>C rs112916171
NM_004621.5(TRPC6):c.*553T>G rs7931399
NM_004621.5(TRPC6):c.*575C>A rs200705719
NM_004621.5(TRPC6):c.*668G>A rs200307747
NM_004621.5(TRPC6):c.*710_*711insTTTA rs145266305
NM_004621.5(TRPC6):c.*792G>A rs201986308
NM_004621.5(TRPC6):c.*821C>T rs886047536
NM_004621.5(TRPC6):c.*970A>G rs146033736
NM_004621.5(TRPC6):c.*9C>T rs187970274
NM_004621.5(TRPC6):c.-10C>A rs191383391
NM_004621.5(TRPC6):c.-125C>T rs201034657
NM_004621.5(TRPC6):c.-143C>T rs886047539
NM_004621.5(TRPC6):c.-218C>T rs56134796
NM_004621.5(TRPC6):c.-243C>T rs199601311
NM_004621.5(TRPC6):c.-254C>G rs3824934
NM_004621.5(TRPC6):c.-317C>G rs886047540
NM_004621.5(TRPC6):c.-319delC rs886047541
NM_004621.5(TRPC6):c.-343C>G rs200074836
NM_004621.5(TRPC6):c.-344C>G rs867713895
NM_004621.5(TRPC6):c.-35G>A rs886047538
NM_004621.5(TRPC6):c.-360T>C rs192759166
NM_004621.5(TRPC6):c.-361A>T rs41302375
NM_004621.5(TRPC6):c.-406C>A rs886047542
NM_004621.5(TRPC6):c.1057C>T (p.Leu353Phe) rs775521973
NM_004621.5(TRPC6):c.1211C>T (p.Ala404Val) rs36111323
NM_004621.5(TRPC6):c.1338C>T (p.His446=) rs112258968
NM_004621.5(TRPC6):c.1344C>A (p.Ala448=) rs554849365
NM_004621.5(TRPC6):c.1677C>T (p.Asp559=) rs552837414
NM_004621.5(TRPC6):c.1683T>C (p.Asn561=) rs12366144
NM_004621.5(TRPC6):c.172C>T (p.Arg58Trp) rs117273916
NM_004621.5(TRPC6):c.1780A>G (p.Ile594Val) rs758348046
NM_004621.5(TRPC6):c.1818T>C (p.Ser606=) rs139187399
NM_004621.5(TRPC6):c.1886G>C (p.Arg629Thr) rs775034304
NM_004621.5(TRPC6):c.1928T>C (p.Met643Thr) rs773581652
NM_004621.5(TRPC6):c.2088C>T (p.Asn696=) rs61739601
NM_004621.5(TRPC6):c.2115C>T (p.Tyr705=) rs61743044
NM_004621.5(TRPC6):c.213T>A (p.Val71=) rs138123801
NM_004621.5(TRPC6):c.2142G>A (p.Thr714=) rs145077205
NM_004621.5(TRPC6):c.2142G>T (p.Thr714=) rs145077205
NM_004621.5(TRPC6):c.2410-11A>G rs886047537
NM_004621.5(TRPC6):c.2508T>C (p.Ser836=) rs377172208
NM_004621.5(TRPC6):c.2529C>T (p.Phe843=) rs72984209
NM_004621.5(TRPC6):c.2574A>C (p.Ile858=) rs751323115
NM_004621.5(TRPC6):c.2620A>T (p.Lys874Ter) rs121434393
NM_004621.5(TRPC6):c.2683C>T (p.Arg895Cys) rs121434394
NM_004621.5(TRPC6):c.2689G>A (p.Glu897Lys) rs121434395
NM_004621.5(TRPC6):c.2712G>A (p.Gln904=) rs12805398
NM_004621.5(TRPC6):c.2770C>T (p.Pro924Ser) rs139330011
NM_004621.5(TRPC6):c.304T>A (p.Phe102Ile) rs201363468
NM_004621.5(TRPC6):c.335C>A (p.Pro112Gln) rs121434390
NM_004621.5(TRPC6):c.336A>C (p.Pro112=) rs201818043
NM_004621.5(TRPC6):c.428A>G (p.Asn143Ser) rs121434391
NM_004621.5(TRPC6):c.43C>T (p.Pro15Ser) rs3802829
NM_004621.5(TRPC6):c.518A>G (p.Tyr173Cys) rs1555003819
NM_004621.5(TRPC6):c.523C>T (p.Arg175Trp) rs869025541
NM_004621.5(TRPC6):c.5G>C (p.Ser2Thr) rs886039885
NM_004621.5(TRPC6):c.673C>G (p.Leu225Val) rs201368333
NM_004621.5(TRPC6):c.739C>T (p.Arg247Trp) rs201859973
NM_004621.5(TRPC6):c.808T>A (p.Ser270Thr) rs121434392
NM_004621.6(TRPC6):c.1747A>G (p.Arg583Gly)
NM_004621.6(TRPC6):c.1886_1887insC (p.Arg629Serfs)
NM_004621.6(TRPC6):c.2009+1G>A
NM_004621.6(TRPC6):c.643C>G (p.Arg215Gly)
NM_004621.6(TRPC6):c.769G>A (p.Asp257Asn)

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