ClinVar Miner

List of variants in gene TRPC3 studied for not provided

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Gene type:
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Total variants: 139
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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.1296C>T (p.Gly432=) rs34119323 0.01795
NM_001130698.2(TRPC3):c.804G>A (p.Lys268=) rs61742537 0.00619
NM_001130698.2(TRPC3):c.2686A>G (p.Ser896Gly) rs142202711 0.00228
NM_001130698.2(TRPC3):c.1707G>A (p.Lys569=) rs34507256 0.00164
NM_001130698.2(TRPC3):c.2127C>A (p.Leu709=) rs140365543 0.00108
NM_001130698.2(TRPC3):c.2469C>T (p.Asn823=) rs139940353 0.00009
NM_001130698.2(TRPC3):c.1268G>A (p.Cys423Tyr) rs199527931 0.00002
NM_001130698.2(TRPC3):c.2285G>A (p.Arg762His) rs142339351 0.00001
NM_001130698.2(TRPC3):c.1049G>T (p.Cys350Phe)
NM_001130698.2(TRPC3):c.1051C>T (p.Arg351Ter)
NM_001130698.2(TRPC3):c.1052G>A (p.Arg351Gln)
NM_001130698.2(TRPC3):c.1122G>A (p.Arg374=)
NM_001130698.2(TRPC3):c.1139G>A (p.Ser380Asn)
NM_001130698.2(TRPC3):c.1141C>T (p.Arg381Cys)
NM_001130698.2(TRPC3):c.1142G>A (p.Arg381His)
NM_001130698.2(TRPC3):c.1156A>G (p.Ile386Val)
NM_001130698.2(TRPC3):c.115G>T (p.Gly39Cys)
NM_001130698.2(TRPC3):c.1177-19A>T
NM_001130698.2(TRPC3):c.1203G>A (p.Gln401=)
NM_001130698.2(TRPC3):c.1214C>T (p.Thr405Met)
NM_001130698.2(TRPC3):c.1253C>A (p.Thr418Asn)
NM_001130698.2(TRPC3):c.1284C>T (p.Val428=)
NM_001130698.2(TRPC3):c.1285G>A (p.Val429Met)
NM_001130698.2(TRPC3):c.1305C>T (p.Phe435=)
NM_001130698.2(TRPC3):c.1312A>T (p.Ile438Phe)
NM_001130698.2(TRPC3):c.1326C>T (p.Ile442=)
NM_001130698.2(TRPC3):c.1328C>T (p.Ala443Val)
NM_001130698.2(TRPC3):c.1330C>T (p.Pro444Ser)
NM_001130698.2(TRPC3):c.1331C>T (p.Pro444Leu)
NM_001130698.2(TRPC3):c.1341G>T (p.Arg447Ser)
NM_001130698.2(TRPC3):c.1342-20T>C
NM_001130698.2(TRPC3):c.1347G>A (p.Gly449=)
NM_001130698.2(TRPC3):c.1386T>C (p.His462=)
NM_001130698.2(TRPC3):c.1395T>G (p.Ser465=)
NM_001130698.2(TRPC3):c.1399A>G (p.Ile467Val)
NM_001130698.2(TRPC3):c.146C>T (p.Pro49Leu)
NM_001130698.2(TRPC3):c.150C>T (p.Arg50=)
NM_001130698.2(TRPC3):c.1558+18A>C
NM_001130698.2(TRPC3):c.1558+4A>T
NM_001130698.2(TRPC3):c.1660A>C (p.Ile554Leu)
NM_001130698.2(TRPC3):c.167G>C (p.Arg56Pro)
NM_001130698.2(TRPC3):c.1704G>A (p.Thr568=)
NM_001130698.2(TRPC3):c.1716G>C (p.Gln572His)
NM_001130698.2(TRPC3):c.1719T>C (p.Tyr573=)
NM_001130698.2(TRPC3):c.1732G>A (p.Val578Ile)
NM_001130698.2(TRPC3):c.174G>T (p.Pro58=)
NM_001130698.2(TRPC3):c.1798G>A (p.Asp600Asn)
NM_001130698.2(TRPC3):c.1849A>G (p.Ile617Val)
NM_001130698.2(TRPC3):c.1885A>G (p.Ile629Val)
NM_001130698.2(TRPC3):c.1894G>T (p.Ala632Ser)
NM_001130698.2(TRPC3):c.191C>T (p.Pro64Leu)
NM_001130698.2(TRPC3):c.1967T>C (p.Leu656Pro)
NM_001130698.2(TRPC3):c.1998T>G (p.Ile666Met)
NM_001130698.2(TRPC3):c.2014T>C (p.Tyr672His)
NM_001130698.2(TRPC3):c.2025C>A (p.Tyr675Ter)
NM_001130698.2(TRPC3):c.204C>T (p.His68=)
NM_001130698.2(TRPC3):c.2057+10del
NM_001130698.2(TRPC3):c.2057+14_2057+18del
NM_001130698.2(TRPC3):c.2058-19del
NM_001130698.2(TRPC3):c.2058-20G>C
NM_001130698.2(TRPC3):c.2113A>T (p.Thr705Ser)
NM_001130698.2(TRPC3):c.2118C>A (p.Ser706=)
NM_001130698.2(TRPC3):c.2118C>T (p.Ser706=)
NM_001130698.2(TRPC3):c.2129A>G (p.Lys710Arg)
NM_001130698.2(TRPC3):c.216-16C>T
NM_001130698.2(TRPC3):c.216-3T>C
NM_001130698.2(TRPC3):c.216-8C>T
NM_001130698.2(TRPC3):c.2163C>T (p.Tyr721=)
NM_001130698.2(TRPC3):c.2164G>A (p.Val722Ile)
NM_001130698.2(TRPC3):c.2175A>G (p.Gly725=)
NM_001130698.2(TRPC3):c.2183A>G (p.Asn728Ser)
NM_001130698.2(TRPC3):c.2253+20A>G
NM_001130698.2(TRPC3):c.2253+8G>A
NM_001130698.2(TRPC3):c.2254-18dup
NM_001130698.2(TRPC3):c.2284C>T (p.Arg762Cys)
NM_001130698.2(TRPC3):c.2310T>C (p.Phe770=)
NM_001130698.2(TRPC3):c.2364A>G (p.Ser788=)
NM_001130698.2(TRPC3):c.2376C>A (p.Phe792Leu)
NM_001130698.2(TRPC3):c.2377A>T (p.Ile793Phe)
NM_001130698.2(TRPC3):c.2384G>A (p.Arg795Gln)
NM_001130698.2(TRPC3):c.2392A>G (p.Asn798Asp)
NM_001130698.2(TRPC3):c.2402A>G (p.Lys801Arg)
NM_001130698.2(TRPC3):c.2407A>C (p.Arg803=)
NM_001130698.2(TRPC3):c.2418G>A (p.Arg806=)
NM_001130698.2(TRPC3):c.2427G>A (p.Lys809=)
NM_001130698.2(TRPC3):c.2430T>C (p.Asp810=)
NM_001130698.2(TRPC3):c.2433A>G (p.Ile811Met)
NM_001130698.2(TRPC3):c.2438T>C (p.Met813Thr)
NM_001130698.2(TRPC3):c.2459C>T (p.Ser820Phe)
NM_001130698.2(TRPC3):c.2463+10G>A
NM_001130698.2(TRPC3):c.2463+9C>T
NM_001130698.2(TRPC3):c.2464-14G>A
NM_001130698.2(TRPC3):c.2468A>C (p.Asn823Thr)
NM_001130698.2(TRPC3):c.2481G>A (p.Gln827=)
NM_001130698.2(TRPC3):c.2539C>T (p.Arg847Cys)
NM_001130698.2(TRPC3):c.2547+15G>C
NM_001130698.2(TRPC3):c.2547+17C>T
NM_001130698.2(TRPC3):c.2547+18G>A
NM_001130698.2(TRPC3):c.2547+3A>G
NM_001130698.2(TRPC3):c.2577T>C (p.Tyr859=)
NM_001130698.2(TRPC3):c.2620G>T (p.Glu874Ter) rs1553936310
NM_001130698.2(TRPC3):c.2624-17dup
NM_001130698.2(TRPC3):c.2647G>T (p.Asp883Tyr)
NM_001130698.2(TRPC3):c.2670A>G (p.Glu890=)
NM_001130698.2(TRPC3):c.2691A>T (p.Gln897His)
NM_001130698.2(TRPC3):c.2701G>A (p.Glu901Lys)
NM_001130698.2(TRPC3):c.2713C>G (p.Leu905Val)
NM_001130698.2(TRPC3):c.2735A>C (p.Lys912Thr)
NM_001130698.2(TRPC3):c.2744C>T (p.Pro915Leu)
NM_001130698.2(TRPC3):c.2752C>T (p.Leu918=)
NM_001130698.2(TRPC3):c.297C>G (p.Ala99=)
NM_001130698.2(TRPC3):c.331G>A (p.Ala111Thr)
NM_001130698.2(TRPC3):c.334G>C (p.Glu112Gln)
NM_001130698.2(TRPC3):c.354C>T (p.Asp118=)
NM_001130698.2(TRPC3):c.393G>A (p.Met131Ile)
NM_001130698.2(TRPC3):c.447C>T (p.Asn149=)
NM_001130698.2(TRPC3):c.459G>A (p.Leu153=)
NM_001130698.2(TRPC3):c.474G>A (p.Glu158=)
NM_001130698.2(TRPC3):c.507G>A (p.Lys169=)
NM_001130698.2(TRPC3):c.531C>T (p.Asp177=)
NM_001130698.2(TRPC3):c.579C>G (p.Ala193=)
NM_001130698.2(TRPC3):c.580A>G (p.Ile194Val)
NM_001130698.2(TRPC3):c.612G>A (p.Lys204=)
NM_001130698.2(TRPC3):c.663C>T (p.Tyr221=)
NM_001130698.2(TRPC3):c.696G>A (p.Pro232=)
NM_001130698.2(TRPC3):c.702C>T (p.Ile234=)
NM_001130698.2(TRPC3):c.760A>C (p.Met254Leu)
NM_001130698.2(TRPC3):c.785C>T (p.Pro262Leu)
NM_001130698.2(TRPC3):c.80_91del (p.23EDEG[1])
NM_001130698.2(TRPC3):c.810G>A (p.Gly270=)
NM_001130698.2(TRPC3):c.816C>T (p.Cys272=)
NM_001130698.2(TRPC3):c.834C>T (p.His278=)
NM_001130698.2(TRPC3):c.878G>A (p.Gly293Glu)
NM_001130698.2(TRPC3):c.87G>C (p.Glu29Asp)
NM_001130698.2(TRPC3):c.888C>G (p.Ser296Arg)
NM_001130698.2(TRPC3):c.890C>G (p.Pro297Arg)
NM_001130698.2(TRPC3):c.913G>A (p.Glu305Lys)
NM_001130698.2(TRPC3):c.987+19C>G

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