Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.113149365T>ACA388794219F10c.1315T>A (p.Trp439Arg)
c.*306T>A (n.*306T>A)
c.1183T>A (p.Trp395Arg)
13g.113149365T>CCA388794221F10c.1315T>C (p.Trp439Arg)
c.*306T>C (n.*306T>C)
c.1183T>C (p.Trp395Arg)
13g.113149365T>GCA388794223F10c.1315T>G (p.Trp439Gly)
c.*306T>G (n.*306T>G)
c.1183T>G (p.Trp395Gly)
13g.113149366G>ACA388794225F10c.1316G>A (p.Trp439Ter)
c.*307G>A (n.*307G>A)
c.1184G>A (p.Trp395Ter)
13g.113149366G>CCA388794226F10c.1316G>C (p.Trp439Ser)
c.*307G>C (n.*307G>C)
c.1184G>C (p.Trp395Ser)
13g.113149366G>TCA388794227F10c.1316G>T (p.Trp439Leu)
c.*307G>T (n.*307G>T)
c.1184G>T (p.Trp395Leu)
13g.113149366_113149367insTCA2623810140F10c.1316_1317insT (p.Trp439CysfsTer8)
c.*307_*308insT (n.*307_*308insT)
c.1184_1185insT (p.Trp395CysfsTer8)
gnomAD v4
13g.113149367G>ACA388794228F10c.1317G>A (p.Trp439Ter)
c.*308G>A (n.*308G>A)
c.1185G>A (p.Trp395Ter)
13g.113149367G>CCA388794229F10c.1317G>C (p.Trp439Cys)
c.*308G>C (n.*308G>C)
c.1185G>C (p.Trp395Cys)
13g.113149367G=CA2120140545F10c.1317G= (p.Trp439=)
c.*308G= (n.*308G=)
c.1185G= (p.Trp395=)
13g.113149367G>TCA388794230F10c.1317G>T (p.Trp439Cys)
c.*308G>T (n.*308G>T)
c.1185G>T (p.Trp395Cys)
13g.113149367_113149376delCA2623810142F10c.1317_1326del (p.Trp439CysfsTer25)
c.*308_*317del (n.*308_*317del)
c.1185_1194del (p.Trp395CysfsTer25)
gnomAD v4
13g.113149367_113149368insTTTTTTTTTTTTAACA612868374F10c.1317_1318insTTTTTTTTTTTTAA (p.Gly440PhefsTer32)
c.*308_*309insTTTTTTTTTTTTAA (n.*308_*309insTTTTTTTTTTTTAA)
c.1185_1186insTTTTTTTTTTTTAA (p.Gly396PhefsTer32)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149368G>ACA388794233F10c.1318G>A (p.Gly440Arg)
c.*309G>A (n.*309G>A)
c.1186G>A (p.Gly396Arg)
13g.113149368G>CCA388794235F10c.1318G>C (p.Gly440Arg)
c.*309G>C (n.*309G>C)
c.1186G>C (p.Gly396Arg)
13g.113149368G=CA2120140549F10c.1318G= (p.Gly440=)
c.*309G= (n.*309G=)
c.1186G= (p.Gly396=)
13g.113149368G>TCA388794231F10c.1318G>T (p.Gly440Ter)
c.*309G>T (n.*309G>T)
c.1186G>T (p.Gly396Ter)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149368_113149376delCA2800665256F10c.1318_1326del (p.Gly440_Gly442del)
c.*309_*317del (n.*309_*317del)
c.1186_1194del (p.Gly396_Gly398del)
13g.113149368_113149369insTTTTTTTTTTAATCA2623810168F10c.1318_1319insTTTTTTTTTTAAT (p.Gly440ValfsTer11)
c.*309_*310insTTTTTTTTTTAAT (n.*309_*310insTTTTTTTTTTAAT)
c.1186_1187insTTTTTTTTTTAAT (p.Gly396ValfsTer11)
gnomAD v4
13g.113149368_113149369insTATTTTTTTTTAATCA2800665263F10c.1318_1319insTATTTTTTTTTAAT (p.Gly440ValfsTer32)
c.*309_*310insTATTTTTTTTTAAT (n.*309_*310insTATTTTTTTTTAAT)
c.1186_1187insTATTTTTTTTTAAT (p.Gly396ValfsTer32)
13g.113149368_113149369insTTGTTTTTTTTAATCA2623810166F10c.1318_1319insTTGTTTTTTTTAAT (p.Gly440ValfsTer32)
c.*309_*310insTTGTTTTTTTTAAT (n.*309_*310insTTGTTTTTTTTAAT)
c.1186_1187insTTGTTTTTTTTAAT (p.Gly396ValfsTer32)
gnomAD v4
13g.113149368_113149369insTTTTGTTTTTTAATCA2800665265F10c.1318_1319insTTTTGTTTTTTAAT (p.Gly440ValfsTer32)
c.*309_*310insTTTTGTTTTTTAAT (n.*309_*310insTTTTGTTTTTTAAT)
c.1186_1187insTTTTGTTTTTTAAT (p.Gly396ValfsTer32)
13g.113149368_113149369insTTTTTTTTTTTAATCA612868376F10c.1318_1319insTTTTTTTTTTTAAT (p.Gly440ValfsTer32)
c.*309_*310insTTTTTTTTTTTAAT (n.*309_*310insTTTTTTTTTTTAAT)
c.1186_1187insTTTTTTTTTTTAAT (p.Gly396ValfsTer32)
dbSNP gnomAD v2 gnomAD v4
13g.113149368_113149369insTTTTTTTTTTTACTCA2623810171F10c.1318_1319insTTTTTTTTTTTACT (p.Gly440ValfsTer32)
c.*309_*310insTTTTTTTTTTTACT (n.*309_*310insTTTTTTTTTTTACT)
c.1186_1187insTTTTTTTTTTTACT (p.Gly396ValfsTer32)
gnomAD v4
13g.113149369G>ACA388794236F10c.1319G>A (p.Gly440Glu)
c.*310G>A (n.*310G>A)
c.1187G>A (p.Gly396Glu)
gnomAD v4
13g.113149369G>CCA388794238F10c.1319G>C (p.Gly440Ala)
c.*310G>C (n.*310G>C)
c.1187G>C (p.Gly396Ala)
dbSNP gnomAD v2 gnomAD v4
13g.113149369G=CA2120140555F10c.1319G= (p.Gly440=)
c.*310G= (n.*310G=)
c.1187G= (p.Gly396=)
13g.113149369G>TCA388794240F10c.1319G>T (p.Gly440Val)
c.*310G>T (n.*310G>T)
c.1187G>T (p.Gly396Val)
13g.113149369_113149370insTTTTTTTTTTAATGCA612868375F10c.1319_1320insTTTTTTTTTTAATG (p.Glu441PhefsTer31)
c.*310_*311insTTTTTTTTTTAATG (n.*310_*311insTTTTTTTTTTAATG)
c.1187_1188insTTTTTTTTTTAATG (p.Glu397PhefsTer31)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149369_113149370insTTTTTTTTTTTAATGCA2800665264F10c.1319_1320insTTTTTTTTTTTAATG (p.Gly441PhefsTer4)
c.*310_*311insTTTTTTTTTTTAATG (n.*310_*311insTTTTTTTTTTTAATG)
c.1187_1188insTTTTTTTTTTTAATG (p.Gly397PhefsTer4)
13g.113149369_113149370insTTTTTTTTTTAATCCA2800665266F10c.1319_1320insTTTTTTTTTTAATC (p.Glu441PhefsTer31)
c.*310_*311insTTTTTTTTTTAATC (n.*310_*311insTTTTTTTTTTAATC)
c.1187_1188insTTTTTTTTTTAATC (p.Glu397PhefsTer31)
13g.113149370A>CCA485424188F10c.1320A>C (p.Gly440=)
c.*311A>C (n.*311A>C)
c.1188A>C (p.Gly396=)
13g.113149370A>GCA485424191F10c.1320A>G (p.Gly440=)
c.*311A>G (n.*311A>G)
c.1188A>G (p.Gly396=)
13g.113149370A>TCA485424189F10c.1320A>T (p.Gly440=)
c.*311A>T (n.*311A>T)
c.1188A>T (p.Gly396=)
13g.113149370_113149376delCA2623810182F10c.1320_1326del (p.Glu441ValfsTer24)
c.*311_*317del (n.*311_*317del)
c.1188_1194del (p.Glu397ValfsTer24)
gnomAD v4
13g.113149370_113149371insTTTTTTTTTAATCA2800665269F10c.1320_1321insTTTTTTTTTAAT (p.Gly440_Glu441insPhePhePheAsn)
c.*311_*312insTTTTTTTTTAAT (n.*311_*312insTTTTTTTTTAAT)
c.1188_1189insTTTTTTTTTAAT (p.Gly396_Glu397insPhePhePheAsn)
13g.113149371G>ACA388794242F10c.1321G>A (p.Glu441Lys)
c.*312G>A (n.*312G>A)
c.1189G>A (p.Glu397Lys)
ClinVar dbSNP
13g.113149371G>CCA388794243F10c.1321G>C (p.Glu441Gln)
c.*312G>C (n.*312G>C)
c.1189G>C (p.Glu397Gln)
13g.113149371G=CA2120140562F10c.1321G= (p.Glu441=)
c.*312G= (n.*312G=)
c.1189G= (p.Glu397=)
13g.113149371G>TCA388794245F10c.1321G>T (p.Glu441Ter)
c.*312G>T (n.*312G>T)
c.1189G>T (p.Glu397Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149372A>CCA388794247F10c.1322A>C (p.Glu441Ala)
c.*313A>C (n.*313A>C)
c.1190A>C (p.Glu397Ala)
13g.113149372A>GCA388794251F10c.1322A>G (p.Glu441Gly)
c.*313A>G (n.*313A>G)
c.1190A>G (p.Glu397Gly)
13g.113149372A>TCA388794249F10c.1322A>T (p.Glu441Val)
c.*313A>T (n.*313A>T)
c.1190A>T (p.Glu397Val)
13g.113149372_113149376delinsAGGGCCA2120140568F10c.1322_1326delinsAGGGC (p.Glu441=)
c.*313_*317delinsAGGGC (n.*313_*317delinsAGGGC)
c.1190_1194delinsAGGGC (p.Glu397=)
13g.113149373G>ACA485424195F10c.1323G>A (p.Glu441=)
c.*314G>A (n.*314G>A)
c.1191G>A (p.Glu397=)
dbSNP gnomAD v4
13g.113149373G>CCA388794253F10c.1323G>C (p.Glu441Asp)
c.*314G>C (n.*314G>C)
c.1191G>C (p.Glu397Asp)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149373G=CA2120140578F10c.1323G= (p.Glu441=)
c.*314G= (n.*314G=)
c.1191G= (p.Glu397=)
13g.113149373G>TCA388794254F10c.1323G>T (p.Glu441Asp)
c.*314G>T (n.*314G>T)
c.1191G>T (p.Glu397Asp)
13g.113149373_113149375delCA2800665271F10c.1323_1325del (p.Glu441_Gly442delinsAsp)
c.*314_*316del (n.*314_*316del)
c.1191_1193del (p.Glu397_Gly398delinsAsp)
13g.113149375delCA2623810190F10c.1325del (p.Gly442AlafsTer25)
c.*316del (n.*316del)
c.1193del (p.Gly398AlafsTer25)
gnomAD v4
13g.113149373_113149376delCA612868378F10c.1323_1326del (p.Glu441AspfsTer25)
c.*314_*317del (n.*314_*317del)
c.1191_1194del (p.Glu397AspfsTer25)
dbSNP gnomAD v2
13g.113149373_113149376delinsGGGCCA2120140572F10c.1323_1326delinsGGGC (p.Glu441=)
c.*314_*317delinsGGGC (n.*314_*317delinsGGGC)
c.1191_1194delinsGGGC (p.Glu397=)
13g.113149373_113149384delCA612868377F10c.1323_1334del (p.Glu441_Arg445delinsAsp)
c.*314_*325del (n.*314_*325del)
c.1191_1202del (p.Glu397_Arg401delinsAsp)
gnomAD v2 gnomAD v4
13g.113149373_113149374insTTTTTTAATCATACCA960419792F10c.1323_1324insTTTTTTAATCATAC (p.Gly442PhefsTer30)
c.*314_*315insTTTTTTAATCATAC (n.*314_*315insTTTTTTAATCATAC)
c.1191_1192insTTTTTTAATCATAC (p.Gly398PhefsTer30)
gnomAD v3 gnomAD v4
13g.113149374G>ACA388794257F10c.1324G>A (p.Gly442Ser)
c.*315G>A (n.*315G>A)
c.1192G>A (p.Gly398Ser)
gnomAD v4
13g.113149374G>CCA388794258F10c.1324G>C (p.Gly442Arg)
c.*315G>C (n.*315G>C)
c.1192G>C (p.Gly398Arg)
13g.113149374G=CA2120140580F10c.1324G= (p.Gly442=)
c.*315G= (n.*315G=)
c.1192G= (p.Gly398=)
13g.113149374G>TCA388794259F10c.1324G>T (p.Gly442Cys)
c.*315G>T (n.*315G>T)
c.1192G>T (p.Gly398Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149374_113149376delCA612868379F10c.1324_1326del (p.Gly442del)
c.*315_*317del (n.*315_*317del)
c.1192_1194del (p.Gly398del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149375G>ACA388794263F10c.1325G>A (p.Gly442Asp)
c.*316G>A (n.*316G>A)
c.1193G>A (p.Gly398Asp)
ClinVar dbSNP gnomAD v4
13g.113149375G>CCA388794264F10c.1325G>C (p.Gly442Ala)
c.*316G>C (n.*316G>C)
c.1193G>C (p.Gly398Ala)
13g.113149375G=CA2120140585F10c.1325G= (p.Gly442=)
c.*316G= (n.*316G=)
c.1193G= (p.Gly398=)
13g.113149375G>TCA388794261F10c.1325G>T (p.Gly442Val)
c.*316G>T (n.*316G>T)
c.1193G>T (p.Gly398Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149375_113149376delCA960419801F10c.1325_1326del (p.Gly442ValfsTer4)
c.*316_*317del (n.*316_*317del)
c.1193_1194del (p.Gly398ValfsTer4)
gnomAD v3 gnomAD v4
13g.113149376delCA2623810225F10c.1326del (p.Cys443ValfsTer24)
c.*317del (n.*317del)
c.1194del (p.Cys399ValfsTer24)
gnomAD v4
13g.113149376C>ACA485424198F10c.1326C>A (p.Gly442=)
c.*317C>A (n.*317C>A)
c.1194C>A (p.Gly398=)
13g.113149376C=CA2120140595F10c.1326C= (p.Gly442=)
c.*317C= (n.*317C=)
c.1194C= (p.Gly398=)
13g.113149376C>GCA7060729F10c.1326C>G (p.Gly442=)
c.*317C>G (n.*317C>G)
c.1194C>G (p.Gly398=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149376C>TCA485424200F10c.1326C>T (p.Gly442=)
c.*317C>T (n.*317C>T)
c.1194C>T (p.Gly398=)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149377T>ACA388794268F10c.1327T>A (p.Cys443Ser)
c.*318T>A (n.*318T>A)
c.1195T>A (p.Cys399Ser)
13g.113149377T>CCA388794269F10c.1327T>C (p.Cys443Arg)
c.*318T>C (n.*318T>C)
c.1195T>C (p.Cys399Arg)
13g.113149377T>GCA388794271F10c.1327T>G (p.Cys443Gly)
c.*318T>G (n.*318T>G)
c.1195T>G (p.Cys399Gly)
13g.113149377_113149378insTTTCA2800665279F10c.1327_1328insTTT (p.Gly442_Cys443insPhe)
c.*318_*319insTTT (n.*318_*319insTTT)
c.1195_1196insTTT (p.Gly398_Cys399insPhe)
13g.113149377_113149379delCA612868380F10c.1327_1329del (p.Cys443del)
c.*318_*320del (n.*318_*320del)
c.1195_1197del (p.Cys399del)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149378delCA960419809F10c.1328del (p.Cys443LeufsTer24)
c.*319del (n.*319del)
c.1196del (p.Cys399LeufsTer24)
gnomAD v3 gnomAD v4
13g.113149378G>ACA388794273F10c.1328G>A (p.Cys443Tyr)
c.*319G>A (n.*319G>A)
c.1196G>A (p.Cys399Tyr)
dbSNP gnomAD v3 gnomAD v4
13g.113149378G>CCA388794274F10c.1328G>C (p.Cys443Ser)
c.*319G>C (n.*319G>C)
c.1196G>C (p.Cys399Ser)
gnomAD v4
13g.113149378G=CA2120140602F10c.1328G= (p.Cys443=)
c.*319G= (n.*319G=)
c.1196G= (p.Cys399=)
13g.113149378G>TCA388794276F10c.1328G>T (p.Cys443Phe)
c.*319G>T (n.*319G>T)
c.1196G>T (p.Cys399Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149380_113149385delCA2623810233F10c.1330_1335del (p.Ala444_Arg445del)
c.*321_*326del (n.*321_*326del)
c.1198_1203del (p.Ala400_Arg401del)
gnomAD v4
13g.113149379T>ACA388794278F10c.1329T>A (p.Cys443Ter)
c.*320T>A (n.*320T>A)
c.1197T>A (p.Cys399Ter)
13g.113149379T>CCA485424735F10c.1329T>C (p.Cys443=)
c.*320T>C (n.*320T>C)
c.1197T>C (p.Cys399=)
13g.113149379T>GCA388794280F10c.1329T>G (p.Cys443Trp)
c.*320T>G (n.*320T>G)
c.1197T>G (p.Cys399Trp)
13g.113149379_113149383delCA2623810235F10c.1329_1333del (p.Cys443TrpfsTer2)
c.*320_*324del (n.*320_*324del)
c.1197_1201del (p.Cys399TrpfsTer2)
gnomAD v4
13g.113149379_113149384delinsTGCCCGCA2120140609F10c.1329_1334delinsTGCCCG (p.Cys443=)
c.*320_*325delinsTGCCCG (n.*320_*325delinsTGCCCG)
c.1197_1202delinsTGCCCG (p.Cys399=)
13g.113149380G>ACA388794281F10c.1330G>A (p.Ala444Thr)
c.*321G>A (n.*321G>A)
c.1198G>A (p.Ala400Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149380G>CCA388794282F10c.1330G>C (p.Ala444Pro)
c.*321G>C (n.*321G>C)
c.1198G>C (p.Ala400Pro)
13g.113149380G=CA2120140615F10c.1330G= (p.Ala444=)
c.*321G= (n.*321G=)
c.1198G= (p.Ala400=)
13g.113149380G>TCA388794283F10c.1330G>T (p.Ala444Ser)
c.*321G>T (n.*321G>T)
c.1198G>T (p.Ala400Ser)
13g.113149380_113149382delCA2623810242F10c.1330_1332del (p.Ala444del)
c.*321_*323del (n.*321_*323del)
c.1198_1200del (p.Ala400del)
gnomAD v4
13g.113149380_113149384delCA612868383F10c.1330_1334del (p.Ala444Ter)
c.*321_*325del (n.*321_*325del)
c.1198_1202del (p.Ala400Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149381_113149384delCA612868384F10c.1331_1334del (p.Ala444ValfsTer22)
c.*322_*325del (n.*322_*325del)
c.1199_1202del (p.Ala400ValfsTer22)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149381_113149391delCA612868382F10c.1331_1341del (p.Ala444GlufsTer?)
c.*322_*332del (n.*322_*332del)
c.1199_1209del (p.Ala400GlufsTer?)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149381C>ACA388794285F10c.1331C>A (p.Ala444Asp)
c.*322C>A (n.*322C>A)
c.1199C>A (p.Ala400Asp)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149381C=CA2120140622F10c.1331C= (p.Ala444=)
c.*322C= (n.*322C=)
c.1199C= (p.Ala400=)
13g.113149381C>GCA388794287F10c.1331C>G (p.Ala444Gly)
c.*322C>G (n.*322C>G)
c.1199C>G (p.Ala400Gly)
13g.113149381C>TCA388794288F10c.1331C>T (p.Ala444Val)
c.*322C>T (n.*322C>T)
c.1199C>T (p.Ala400Val)
dbSNP gnomAD v3 gnomAD v4
13g.113149381_113149383delCA2800665283F10c.1331_1333del (p.Ala444_Arg445delinsGly)
c.*322_*324del (n.*322_*324del)
c.1199_1201del (p.Ala400_Arg401delinsGly)
13g.113149382C>ACA485424753F10c.1332C>A (p.Ala444=)
c.*323C>A (n.*323C>A)
c.1200C>A (p.Ala400=)
13g.113149382C>GCA485424755F10c.1332C>G (p.Ala444=)
c.*323C>G (n.*323C>G)
c.1200C>G (p.Ala400=)
gnomAD v4
13g.113149382C>TCA485424757F10c.1332C>T (p.Ala444=)
c.*323C>T (n.*323C>T)
c.1200C>T (p.Ala400=)
13g.113149382_113149384delCA612868385F10c.1332_1334del (p.Arg445del)
c.*323_*325del (n.*323_*325del)
c.1200_1202del (p.Arg401del)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149383C>ACA388794290F10c.1333C>A (p.Arg445Ser)
c.*324C>A (n.*324C>A)
c.1201C>A (p.Arg401Ser)
gnomAD v4
13g.113149383C=CA2120140628F10c.1333C= (p.Arg445=)
c.*324C= (n.*324C=)
c.1201C= (p.Arg401=)
13g.113149383C>GCA388794291F10c.1333C>G (p.Arg445Gly)
c.*324C>G (n.*324C>G)
c.1201C>G (p.Arg401Gly)
gnomAD v4
13g.113149383C>TCA7060730F10c.1333C>T (p.Arg445Cys)
c.*324C>T (n.*324C>T)
c.1201C>T (p.Arg401Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.113149384G>ACA388794293F10c.1334G>A (p.Arg445His)
c.*325G>A (n.*325G>A)
c.1202G>A (p.Arg401His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149384G>CCA388794295F10c.1334G>C (p.Arg445Pro)
c.*325G>C (n.*325G>C)
c.1202G>C (p.Arg401Pro)
13g.113149384G=CA2120140635F10c.1334G= (p.Arg445=)
c.*325G= (n.*325G=)
c.1202G= (p.Arg401=)
13g.113149384G>TCA388794296F10c.1334G>T (p.Arg445Leu)
c.*325G>T (n.*325G>T)
c.1202G>T (p.Arg401Leu)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149384_113149395delCA612868386F10c.1334_1345del (p.Arg445_Tyr449delinsHis)
c.*325_*336del (n.*325_*336del)
c.1202_1213del (p.Arg401_Tyr405delinsHis)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149384_113149385insATGACA2800665289F10c.1334_1335insATGA (p.Lys446Ter)
c.*325_*326insATGA (n.*325_*326insATGA)
c.1202_1203insATGA (p.Lys402Ter)
13g.113149385T>ACA485424774F10c.1335T>A (p.Arg445=)
c.*326T>A (n.*326T>A)
c.1203T>A (p.Arg401=)
13g.113149385T>CCA485424778F10c.1335T>C (p.Arg445=)
c.*326T>C (n.*326T>C)
c.1203T>C (p.Arg401=)
dbSNP
13g.113149385T>GCA485424779F10c.1335T>G (p.Arg445=)
c.*326T>G (n.*326T>G)
c.1203T>G (p.Arg401=)
gnomAD v4
13g.113149385T=CA2120140641F10c.1335T= (p.Arg445=)
c.*326T= (n.*326T=)
c.1203T= (p.Arg401=)
13g.113149385_113149386insTTCA612868387F10c.1335_1336insTT (p.Lys446LeufsTer22)
c.*326_*327insTT (n.*326_*327insTT)
c.1203_1204insTT (p.Lys402LeufsTer22)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149385_113149386insTTTCA612868388F10c.1335_1336insTTT (p.Arg445_Lys446insPhe)
c.*326_*327insTTT (n.*326_*327insTTT)
c.1203_1204insTTT (p.Arg401_Lys402insPhe)
gnomAD v2
13g.113149385_113149386insTTTTTCA2623810275F10c.1335_1336insTTTTT (p.Lys446PhefsTer23)
c.*326_*327insTTTTT (n.*326_*327insTTTTT)
c.1203_1204insTTTTT (p.Lys402PhefsTer23)
gnomAD v4
13g.113149385_113149386insTGTTTTCA2800665290F10c.1335_1336insTGTTTT (p.Arg445_Lys446insCysPhe)
c.*326_*327insTGTTTT (n.*326_*327insTGTTTT)
c.1203_1204insTGTTTT (p.Arg401_Lys402insCysPhe)
13g.113149385_113149386insTTTTTTTTTCA612868389F10c.1335_1336insTTTTTTTTT (p.Arg445_Lys446insPhePhePhe)
c.*326_*327insTTTTTTTTT (n.*326_*327insTTTTTTTTT)
c.1203_1204insTTTTTTTTT (p.Arg401_Lys402insPhePhePhe)
gnomAD v2
13g.113149385_113149390delinsTAAGGGCA2120140639F10c.1335_1340delinsTAAGGG (p.Arg445=)
c.*326_*331delinsTAAGGG (n.*326_*331delinsTAAGGG)
c.1203_1208delinsTAAGGG (p.Arg401=)
13g.113149386A>CCA388794299F10c.1336A>C (p.Lys446Gln)
c.*327A>C (n.*327A>C)
c.1204A>C (p.Lys402Gln)
13g.113149386A>GCA388794301F10c.1336A>G (p.Lys446Glu)
c.*327A>G (n.*327A>G)
c.1204A>G (p.Lys402Glu)
13g.113149386A>TCA388794303F10c.1336A>T (p.Lys446Ter)
c.*327A>T (n.*327A>T)
c.1204A>T (p.Lys402Ter)
13g.113149386_113149390delCA612868390F10c.1336_1340del (p.Lys446GlufsTer?)
c.*327_*331del (n.*327_*331del)
c.1204_1208del (p.Lys402GlufsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149387A>CCA388794305F10c.1337A>C (p.Lys446Thr)
c.*328A>C (n.*328A>C)
c.1205A>C (p.Lys402Thr)
gnomAD v2 gnomAD v4 COSMIC
13g.113149387A>GCA388794307F10c.1337A>G (p.Lys446Arg)
c.*328A>G (n.*328A>G)
c.1205A>G (p.Lys402Arg)
13g.113149387A>TCA388794308F10c.1337A>T (p.Lys446Met)
c.*328A>T (n.*328A>T)
c.1205A>T (p.Lys402Met)
gnomAD v4
13g.113149387_113149389delinsAGGCA2120140645F10c.1337_1339delinsAGG (p.Lys446=)
c.*328_*330delinsAGG (n.*328_*330delinsAGG)
c.1205_1207delinsAGG (p.Lys402=)
13g.113149387_113149388insTCATACCA2800665298F10c.1337_1338insTCATAC (p.Lys446delinsAsnHisThr)
c.*328_*329insTCATAC (n.*328_*329insTCATAC)
c.1205_1206insTCATAC (p.Lys402delinsAsnHisThr)
13g.113149387_113149388insTGATACCA2623810294F10c.1337_1338insTGATAC (p.Lys446delinsAsnAspThr)
c.*328_*329insTGATAC (n.*328_*329insTGATAC)
c.1205_1206insTGATAC (p.Lys402delinsAsnAspThr)
gnomAD v4
13g.113149388G>ACA7060731F10c.1338G>A (p.Lys446=)
c.*329G>A (n.*329G>A)
c.1206G>A (p.Lys402=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149388G>CCA388794311F10c.1338G>C (p.Lys446Asn)
c.*329G>C (n.*329G>C)
c.1206G>C (p.Lys402Asn)
13g.113149388G=CA2120140649F10c.1338G= (p.Lys446=)
c.*329G= (n.*329G=)
c.1206G= (p.Lys402=)
13g.113149388G>TCA388794313F10c.1338G>T (p.Lys446Asn)
c.*329G>T (n.*329G>T)
c.1206G>T (p.Lys402Asn)
gnomAD v4
13g.113149390_113149391delCA612868391F10c.1340_1341del (p.Gly447GlufsTer?)
c.*331_*332del (n.*331_*332del)
c.1208_1209del (p.Gly403GlufsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149389G>ACA7060732F10c.1339G>A (p.Gly447Arg)
c.*330G>A (n.*330G>A)
c.1207G>A (p.Gly403Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.113149389G>CCA388794317F10c.1339G>C (p.Gly447Arg)
c.*330G>C (n.*330G>C)
c.1207G>C (p.Gly403Arg)
13g.113149389G=CA2120140650F10c.1339G= (p.Gly447=)
c.*330G= (n.*330G=)
c.1207G= (p.Gly403=)
13g.113149389G>TCA388794315F10c.1339G>T (p.Gly447Trp)
c.*330G>T (n.*330G>T)
c.1207G>T (p.Gly403Trp)
13g.113149390G>ACA388794319F10c.1340G>A (p.Gly447Glu)
c.*331G>A (n.*331G>A)
c.1208G>A (p.Gly403Glu)
13g.113149390G>CCA388794320F10c.1340G>C (p.Gly447Ala)
c.*331G>C (n.*331G>C)
c.1208G>C (p.Gly403Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149390G=CA2120140653F10c.1340G= (p.Gly447=)
c.*331G= (n.*331G=)
c.1208G= (p.Gly403=)
13g.113149390G>TCA388794322F10c.1340G>T (p.Gly447Val)
c.*331G>T (n.*331G>T)
c.1208G>T (p.Gly403Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149391_113149394delCA2623810313F10c.1341_1344del (p.Lys448ThrfsTer18)
c.*332_*335del (n.*332_*335del)
c.1209_1212del (p.Lys404ThrfsTer18)
gnomAD v4
13g.113149391G>ACA256478746F10c.1341G>A (p.Gly447=)
c.*332G>A (n.*332G>A)
c.1209G>A (p.Gly403=)
dbSNP
13g.113149391G>CCA485424819F10c.1341G>C (p.Gly447=)
c.*332G>C (n.*332G>C)
c.1209G>C (p.Gly403=)
13g.113149391G=CA2120140658F10c.1341G= (p.Gly447=)
c.*332G= (n.*332G=)
c.1209G= (p.Gly403=)
13g.113149391G>TCA485424823F10c.1341G>T (p.Gly447=)
c.*332G>T (n.*332G>T)
c.1209G>T (p.Gly403=)
13g.113149392A>CCA388794324F10c.1342A>C (p.Lys448Gln)
c.*333A>C (n.*333A>C)
c.1210A>C (p.Lys404Gln)
13g.113149392A>GCA388794326F10c.1342A>G (p.Lys448Glu)
c.*333A>G (n.*333A>G)
c.1210A>G (p.Lys404Glu)
13g.113149392A>TCA388794327F10c.1342A>T (p.Lys448Ter)
c.*333A>T (n.*333A>T)
c.1210A>T (p.Lys404Ter)
13g.113149392_113149394delinsAAGCA2120140661F10c.1342_1344delinsAAG (p.Lys448=)
c.*333_*335delinsAAG (n.*333_*335delinsAAG)
c.1210_1212delinsAAG (p.Lys404=)
13g.113149392_113149393insCCCA612868393F10c.1342_1343insCC (p.Lys448ThrfsTer20)
c.*333_*334insCC (n.*333_*334insCC)
c.1210_1211insCC (p.Lys404ThrfsTer20)
gnomAD v2 gnomAD v4
13g.113149393A>CCA388794332F10c.1343A>C (p.Lys448Thr)
c.*334A>C (n.*334A>C)
c.1211A>C (p.Lys404Thr)
gnomAD v4
13g.113149393A>GCA388794329F10c.1343A>G (p.Lys448Arg)
c.*334A>G (n.*334A>G)
c.1211A>G (p.Lys404Arg)
13g.113149393A>TCA388794331F10c.1343A>T (p.Lys448Met)
c.*334A>T (n.*334A>T)
c.1211A>T (p.Lys404Met)
gnomAD v2 gnomAD v3 gnomAD v4
13g.113149393_113149394delCA612868392F10c.1343_1344del (p.Lys448IlefsTer?)
c.*334_*335del (n.*334_*335del)
c.1211_1212del (p.Lys404IlefsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149394G>ACA485424838F10c.1344G>A (p.Lys448=)
c.*335G>A (n.*335G>A)
c.1212G>A (p.Lys404=)
13g.113149394G>CCA388794334F10c.1344G>C (p.Lys448Asn)
c.*335G>C (n.*335G>C)
c.1212G>C (p.Lys404Asn)
gnomAD v4
13g.113149394G=CA2120140667F10c.1344G= (p.Lys448=)
c.*335G= (n.*335G=)
c.1212G= (p.Lys404=)
13g.113149394G>TCA388794336F10c.1344G>T (p.Lys448Asn)
c.*335G>T (n.*335G>T)
c.1212G>T (p.Lys404Asn)
13g.113149394_113149395delCA612868394F10c.1344_1345del (p.Tyr449ArgfsTer?)
c.*335_*336del (n.*335_*336del)
c.1212_1213del (p.Tyr405ArgfsTer?)
gnomAD v2 gnomAD v4
13g.113149394_113149395insACA612868395F10c.1344_1345insA (p.Tyr449IlefsTer?)
c.*335_*336insA (n.*335_*336insA)
c.1212_1213insA (p.Tyr405IlefsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149395T>ACA388794338F10c.1345T>A (p.Tyr449Asn)
c.*336T>A (n.*336T>A)
c.1213T>A (p.Tyr405Asn)
gnomAD v4
13g.113149395T>CCA388794339F10c.1345T>C (p.Tyr449His)
c.*336T>C (n.*336T>C)
c.1213T>C (p.Tyr405His)
13g.113149395T>GCA388794342F10c.1345T>G (p.Tyr449Asp)
c.*336T>G (n.*336T>G)
c.1213T>G (p.Tyr405Asp)
13g.113149396A=CA2120140669F10c.1346A= (p.Tyr449=)
c.*337A= (n.*337A=)
c.1214A= (p.Tyr405=)
13g.113149396A>CCA388794344F10c.1346A>C (p.Tyr449Ser)
c.*337A>C (n.*337A>C)
c.1214A>C (p.Tyr405Ser)
dbSNP gnomAD v2 gnomAD v4
13g.113149396A>GCA388794347F10c.1346A>G (p.Tyr449Cys)
c.*337A>G (n.*337A>G)
c.1214A>G (p.Tyr405Cys)
13g.113149396A>TCA388794345F10c.1346A>T (p.Tyr449Phe)
c.*337A>T (n.*337A>T)
c.1214A>T (p.Tyr405Phe)
13g.113149397C>ACA388794349F10c.1347C>A (p.Tyr449Ter)
c.*338C>A (n.*338C>A)
c.1215C>A (p.Tyr405Ter)
13g.113149397C=CA2120140673F10c.1347C= (p.Tyr449=)
c.*338C= (n.*338C=)
c.1215C= (p.Tyr405=)
13g.113149397C>GCA388794351F10c.1347C>G (p.Tyr449Ter)
c.*338C>G (n.*338C>G)
c.1215C>G (p.Tyr405Ter)
13g.113149397C>TCA485424857F10c.1347C>T (p.Tyr449=)
c.*338C>T (n.*338C>T)
c.1215C>T (p.Tyr405=)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.113149397dupCA612868396F10c.1347dup (p.Gly450ArgfsTer?)
c.*338dup (n.*338dup)
c.1215dup (p.Gly406ArgfsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149398G>ACA388794353F10c.1348G>A (p.Gly450Arg)
c.*339G>A (n.*339G>A)
c.1216G>A (p.Gly406Arg)
ClinVar dbSNP gnomAD v4 COSMIC
13g.113149398G>CCA388794355F10c.1348G>C (p.Gly450Arg)
c.*339G>C (n.*339G>C)
c.1216G>C (p.Gly406Arg)
13g.113149398G=CA2120140680F10c.1348G= (p.Gly450=)
c.*339G= (n.*339G=)
c.1216G= (p.Gly406=)
13g.113149398G>TCA388794356F10c.1348G>T (p.Gly450Trp)
c.*339G>T (n.*339G>T)
c.1216G>T (p.Gly406Trp)
13g.113149399G>ACA388794357F10c.1349G>A (p.Gly450Glu)
c.*340G>A (n.*340G>A)
c.1217G>A (p.Gly406Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149399G>CCA388794358F10c.1349G>C (p.Gly450Ala)
c.*340G>C (n.*340G>C)
c.1217G>C (p.Gly406Ala)
13g.113149399G=CA2120140688F10c.1349G= (p.Gly450=)
c.*340G= (n.*340G=)
c.1217G= (p.Gly406=)
13g.113149399G>TCA388794359F10c.1349G>T (p.Gly450Val)
c.*340G>T (n.*340G>T)
c.1217G>T (p.Gly406Val)
dbSNP gnomAD v2
13g.113149399_113149400insCGAACACCGACA2623810349F10c.1349_1350insCGAACACCGA (p.Ile451GlufsTer?)
c.*340_*341insCGAACACCGA (n.*340_*341insCGAACACCGA)
c.1217_1218insCGAACACCGA (p.Ile407GlufsTer?)
gnomAD v4
13g.113149399_113149400insCGACCACCGACA612868397F10c.1349_1350insCGACCACCGA (p.Ile451AspfsTer?)
c.*340_*341insCGACCACCGA (n.*340_*341insCGACCACCGA)
c.1217_1218insCGACCACCGA (p.Ile407AspfsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149399_113149400insCGACCTCCGACA2623810347F10c.1349_1350insCGACCTCCGA (p.Ile451AspfsTer?)
c.*340_*341insCGACCTCCGA (n.*340_*341insCGACCTCCGA)
c.1217_1218insCGACCTCCGA (p.Ile407AspfsTer?)
gnomAD v4
13g.113149399_113149400insCGACGACCGACA2800665312F10c.1349_1350insCGACGACCGA (p.Ile451AspfsTer?)
c.*340_*341insCGACGACCGA (n.*340_*341insCGACGACCGA)
c.1217_1218insCGACGACCGA (p.Ile407AspfsTer?)
13g.113149400G>ACA7060733F10c.1350G>A (p.Gly450=)
c.*341G>A (n.*341G>A)
c.1218G>A (p.Gly406=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149400G>CCA485424862F10c.1350G>C (p.Gly450=)
c.*341G>C (n.*341G>C)
c.1218G>C (p.Gly406=)
gnomAD v4
13g.113149400G=CA2120140693F10c.1350G= (p.Gly450=)
c.*341G= (n.*341G=)
c.1218G= (p.Gly406=)
13g.113149400G>TCA485424864F10c.1350G>T (p.Gly450=)
c.*341G>T (n.*341G>T)
c.1218G>T (p.Gly406=)
13g.113149401A=CA2120140696F10c.1351A= (p.Ile451=)
c.*342A= (n.*342A=)
c.1219A= (p.Ile407=)
13g.113149401A>CCA7060734F10c.1351A>C (p.Ile451Leu)
c.*342A>C (n.*342A>C)
c.1219A>C (p.Ile407Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149401A>GCA388794363F10c.1351A>G (p.Ile451Val)
c.*342A>G (n.*342A>G)
c.1219A>G (p.Ile407Val)
13g.113149401A>TCA388794364F10c.1351A>T (p.Ile451Phe)
c.*342A>T (n.*342A>T)
c.1219A>T (p.Ile407Phe)
13g.113149402T>ACA388794369F10c.1352T>A (p.Ile451Asn)
c.*343T>A (n.*343T>A)
c.1220T>A (p.Ile407Asn)
13g.113149402T>CCA388794370F10c.1352T>C (p.Ile451Thr)
c.*343T>C (n.*343T>C)
c.1220T>C (p.Ile407Thr)
13g.113149402T>GCA388794367F10c.1352T>G (p.Ile451Ser)
c.*343T>G (n.*343T>G)
c.1220T>G (p.Ile407Ser)
13g.113149403C>ACA485424878F10c.1353C>A (p.Ile451=)
c.*344C>A (n.*344C>A)
c.1221C>A (p.Ile407=)
13g.113149403C>GCA388794372F10c.1353C>G (p.Ile451Met)
c.*344C>G (n.*344C>G)
c.1221C>G (p.Ile407Met)
13g.113149403C>TCA485424882F10c.1353C>T (p.Ile451=)
c.*344C>T (n.*344C>T)
c.1221C>T (p.Ile407=)
13g.113149404T>ACA388794375F10c.1354T>A (p.Tyr452Asn)
c.*345T>A (n.*345T>A)
c.1222T>A (p.Tyr408Asn)
13g.113149404T>CCA388794374F10c.1354T>C (p.Tyr452His)
c.*345T>C (n.*345T>C)
c.1222T>C (p.Tyr408His)
13g.113149404T>GCA388794377F10c.1354T>G (p.Tyr452Asp)
c.*345T>G (n.*345T>G)
c.1222T>G (p.Tyr408Asp)
13g.113149404_113149418delinsTACACCAAGGTCACCCA2120140698F10c.1354_1368delinsTACACCAAGGTCACC (p.Tyr452=)
c.*345_*359delinsTACACCAAGGTCACC (n.*345_*359delinsTACACCAAGGTCACC)
c.1222_1236delinsTACACCAAGGTCACC (p.Tyr408=)
13g.113149405A>CCA388794378F10c.1355A>C (p.Tyr452Ser)
c.*346A>C (n.*346A>C)
c.1223A>C (p.Tyr408Ser)
13g.113149405A>GCA388794382F10c.1355A>G (p.Tyr452Cys)
c.*346A>G (n.*346A>G)
c.1223A>G (p.Tyr408Cys)
13g.113149405A>TCA388794380F10c.1355A>T (p.Tyr452Phe)
c.*346A>T (n.*346A>T)
c.1223A>T (p.Tyr408Phe)
13g.113149405_113149418delCA2120140701F10c.1355_1368del (p.Tyr452CysfsTer?)
c.*346_*359del (n.*346_*359del)
c.1223_1236del (p.Tyr408CysfsTer?)
dbSNP
13g.113149406C>ACA388794384F10c.1356C>A (p.Tyr452Ter)
c.*347C>A (n.*347C>A)
c.1224C>A (p.Tyr408Ter)
13g.113149406C>GCA388794385F10c.1356C>G (p.Tyr452Ter)
c.*347C>G (n.*347C>G)
c.1224C>G (p.Tyr408Ter)
13g.113149406C>TCA485424900F10c.1356C>T (p.Tyr452=)
c.*347C>T (n.*347C>T)
c.1224C>T (p.Tyr408=)
gnomAD v4
13g.113149407A>CCA388794387F10c.1357A>C (p.Thr453Pro)
c.*348A>C (n.*348A>C)
c.1225A>C (p.Thr409Pro)
13g.113149407A>GCA388794388F10c.1357A>G (p.Thr453Ala)
c.*348A>G (n.*348A>G)
c.1225A>G (p.Thr409Ala)
13g.113149407A>TCA388794389F10c.1357A>T (p.Thr453Ser)
c.*348A>T (n.*348A>T)
c.1225A>T (p.Thr409Ser)
13g.113149408C>ACA388794391F10c.1358C>A (p.Thr453Asn)
c.*349C>A (n.*349C>A)
c.1226C>A (p.Thr409Asn)
13g.113149408C=CA2120140705F10c.1358C= (p.Thr453=)
c.*349C= (n.*349C=)
c.1226C= (p.Thr409=)
13g.113149408C>GCA256478749F10c.1358C>G (p.Thr453Ser)
c.*349C>G (n.*349C>G)
c.1226C>G (p.Thr409Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149408C>TCA388794393F10c.1358C>T (p.Thr453Ile)
c.*349C>T (n.*349C>T)
c.1226C>T (p.Thr409Ile)
dbSNP
13g.113149409C>ACA485424917F10c.1359C>A (p.Thr453=)
c.*350C>A (n.*350C>A)
c.1227C>A (p.Thr409=)
13g.113149409C=CA2120140708F10c.1359C= (p.Thr453=)
c.*350C= (n.*350C=)
c.1227C= (p.Thr409=)
13g.113149409C>GCA485424919F10c.1359C>G (p.Thr453=)
c.*350C>G (n.*350C>G)
c.1227C>G (p.Thr409=)
gnomAD v4
13g.113149409C>TCA485424922F10c.1359C>T (p.Thr453=)
c.*350C>T (n.*350C>T)
c.1227C>T (p.Thr409=)
dbSNP
13g.113149410A=CA2120140713F10c.1360A= (p.Lys454=)
c.*351A= (n.*351A=)
c.1228A= (p.Lys410=)
13g.113149410A>CCA388794394F10c.1360A>C (p.Lys454Gln)
c.*351A>C (n.*351A>C)
c.1228A>C (p.Lys410Gln)
13g.113149410A>GCA388794395F10c.1360A>G (p.Lys454Glu)
c.*351A>G (n.*351A>G)
c.1228A>G (p.Lys410Glu)
gnomAD v4
13g.113149410A>TCA388794396F10c.1360A>T (p.Lys454Ter)
c.*351A>T (n.*351A>T)
c.1228A>T (p.Lys410Ter)
dbSNP gnomAD v3 gnomAD v4
13g.113149411A>CCA388794397F10c.1361A>C (p.Lys454Thr)
c.*352A>C (n.*352A>C)
c.1229A>C (p.Lys410Thr)
13g.113149411A>GCA388794398F10c.1361A>G (p.Lys454Arg)
c.*352A>G (n.*352A>G)
c.1229A>G (p.Lys410Arg)
13g.113149411A>TCA388794399F10c.1361A>T (p.Lys454Met)
c.*352A>T (n.*352A>T)
c.1229A>T (p.Lys410Met)
13g.113149411_113149412insCACACCCAACACACA2800665314F10c.1361_1362insCACACCCAACACA (p.Lys454AsnfsTer?)
c.*352_*353insCACACCCAACACA (n.*352_*353insCACACCCAACACA)
c.1229_1230insCACACCCAACACA (p.Lys410AsnfsTer?)
13g.113149412G>ACA485424940F10c.1362G>A (p.Lys454=)
c.*353G>A (n.*353G>A)
c.1230G>A (p.Lys410=)
dbSNP gnomAD v3 gnomAD v4
13g.113149412G>CCA388794403F10c.1362G>C (p.Lys454Asn)
c.*353G>C (n.*353G>C)
c.1230G>C (p.Lys410Asn)
gnomAD v4
13g.113149412G=CA2120140716F10c.1362G= (p.Lys454=)
c.*353G= (n.*353G=)
c.1230G= (p.Lys410=)
13g.113149412G>TCA388794401F10c.1362G>T (p.Lys454Asn)
c.*353G>T (n.*353G>T)
c.1230G>T (p.Lys410Asn)
13g.113149413G>ACA388794404F10c.1363G>A (p.Val455Ile)
c.*354G>A (n.*354G>A)
c.1231G>A (p.Val411Ile)
dbSNP
13g.113149413G>CCA388794406F10c.1363G>C (p.Val455Leu)
c.*354G>C (n.*354G>C)
c.1231G>C (p.Val411Leu)
13g.113149413G=CA2120140720F10c.1363G= (p.Val455=)
c.*354G= (n.*354G=)
c.1231G= (p.Val411=)
13g.113149413G>TCA388794408F10c.1363G>T (p.Val455Phe)
c.*354G>T (n.*354G>T)
c.1231G>T (p.Val411Phe)
13g.113149414T>ACA388794410F10c.1364T>A (p.Val455Asp)
c.*355T>A (n.*355T>A)
c.1232T>A (p.Val411Asp)
13g.113149414T>CCA388794411F10c.1364T>C (p.Val455Ala)
c.*355T>C (n.*355T>C)
c.1232T>C (p.Val411Ala)
dbSNP gnomAD v4
13g.113149414T>GCA388794413F10c.1364T>G (p.Val455Gly)
c.*355T>G (n.*355T>G)
c.1232T>G (p.Val411Gly)
13g.113149414T=CA2120140724F10c.1364T= (p.Val455=)
c.*355T= (n.*355T=)
c.1232T= (p.Val411=)
13g.113149415C>ACA485424962F10c.1365C>A (p.Val455=)
c.*356C>A (n.*356C>A)
c.1233C>A (p.Val411=)
13g.113149415C>GCA485424964F10c.1365C>G (p.Val455=)
c.*356C>G (n.*356C>G)
c.1233C>G (p.Val411=)
13g.113149415C>TCA485424968F10c.1365C>T (p.Val455=)
c.*356C>T (n.*356C>T)
c.1233C>T (p.Val411=)
gnomAD v4
13g.113149416A>CCA388794415F10c.1366A>C (p.Thr456Pro)
c.*357A>C (n.*357A>C)
c.1234A>C (p.Thr412Pro)
13g.113149416A>GCA388794417F10c.1366A>G (p.Thr456Ala)
c.*357A>G (n.*357A>G)
c.1234A>G (p.Thr412Ala)
13g.113149416A>TCA388794418F10c.1366A>T (p.Thr456Ser)
c.*357A>T (n.*357A>T)
c.1234A>T (p.Thr412Ser)
13g.113149417C>ACA388794420F10c.1367C>A (p.Thr456Asn)
c.*358C>A (n.*358C>A)
c.1235C>A (p.Thr412Asn)
13g.113149417C=CA2120140730F10c.1367C= (p.Thr456=)
c.*358C= (n.*358C=)
c.1235C= (p.Thr412=)
13g.113149417C>GCA388794422F10c.1367C>G (p.Thr456Ser)
c.*358C>G (n.*358C>G)
c.1235C>G (p.Thr412Ser)
13g.113149417C>TCA388794423F10c.1367C>T (p.Thr456Ile)
c.*358C>T (n.*358C>T)
c.1235C>T (p.Thr412Ile)
dbSNP
13g.113149418C>ACA485424985F10c.1368C>A (p.Thr456=)
c.*359C>A (n.*359C>A)
c.1236C>A (p.Thr412=)
13g.113149418C=CA2120140736F10c.1368C= (p.Thr456=)
c.*359C= (n.*359C=)
c.1236C= (p.Thr412=)
13g.113149418C>GCA485424989F10c.1368C>G (p.Thr456=)
c.*359C>G (n.*359C>G)
c.1236C>G (p.Thr412=)
gnomAD v4
13g.113149418C>TCA7060735F10c.1368C>T (p.Thr456=)
c.*359C>T (n.*359C>T)
c.1236C>T (p.Thr412=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.113149419G>ACA7060736F10c.1369G>A (p.Ala457Thr)
c.*360G>A (n.*360G>A)
c.1237G>A (p.Ala413Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149419G>CCA388794424F10c.1369G>C (p.Ala457Pro)
c.*360G>C (n.*360G>C)
c.1237G>C (p.Ala413Pro)
13g.113149419G=CA2120140738F10c.1369G= (p.Ala457=)
c.*360G= (n.*360G=)
c.1237G= (p.Ala413=)
13g.113149419G>TCA388794426F10c.1369G>T (p.Ala457Ser)
c.*360G>T (n.*360G>T)
c.1237G>T (p.Ala413Ser)
dbSNP
13g.113149420C>ACA388794428F10c.1370C>A (p.Ala457Asp)
c.*361C>A (n.*361C>A)
c.1238C>A (p.Ala413Asp)
13g.113149420C>GCA388794430F10c.1370C>G (p.Ala457Gly)
c.*361C>G (n.*361C>G)
c.1238C>G (p.Ala413Gly)
13g.113149420C>TCA388794431F10c.1370C>T (p.Ala457Val)
c.*361C>T (n.*361C>T)
c.1238C>T (p.Ala413Val)
gnomAD v4
13g.113149421C>ACA485425005F10c.1371C>A (p.Ala457=)
c.*362C>A (n.*362C>A)
c.1239C>A (p.Ala413=)
13g.113149421C=CA2120140741F10c.1371C= (p.Ala457=)
c.*362C= (n.*362C=)
c.1239C= (p.Ala413=)
13g.113149421C>GCA485425007F10c.1371C>G (p.Ala457=)
c.*362C>G (n.*362C>G)
c.1239C>G (p.Ala413=)
13g.113149421C>TCA485425010F10c.1371C>T (p.Ala457=)
c.*362C>T (n.*362C>T)
c.1239C>T (p.Ala413=)
dbSNP gnomAD v3 gnomAD v4
13g.113149422T>ACA388794434F10c.1372T>A (p.Phe458Ile)
c.*363T>A (n.*363T>A)
c.1240T>A (p.Phe414Ile)
13g.113149422T>CCA388794436F10c.1372T>C (p.Phe458Leu)
c.*363T>C (n.*363T>C)
c.1240T>C (p.Phe414Leu)
dbSNP gnomAD v3 gnomAD v4
13g.113149422T>GCA388794437F10c.1372T>G (p.Phe458Val)
c.*363T>G (n.*363T>G)
c.1240T>G (p.Phe414Val)
13g.113149422T=CA2120140744F10c.1372T= (p.Phe458=)
c.*363T= (n.*363T=)
c.1240T= (p.Phe414=)
13g.113149423T>ACA388794442F10c.1373T>A (p.Phe458Tyr)
c.*364T>A (n.*364T>A)
c.1241T>A (p.Phe414Tyr)
13g.113149423T>CCA388794439F10c.1373T>C (p.Phe458Ser)
c.*364T>C (n.*364T>C)
c.1241T>C (p.Phe414Ser)
13g.113149423T>GCA388794441F10c.1373T>G (p.Phe458Cys)
c.*364T>G (n.*364T>G)
c.1241T>G (p.Phe414Cys)
13g.113149424C>ACA388794444F10c.1374C>A (p.Phe458Leu)
c.*365C>A (n.*365C>A)
c.1242C>A (p.Phe414Leu)
13g.113149424C>GCA388794446F10c.1374C>G (p.Phe458Leu)
c.*365C>G (n.*365C>G)
c.1242C>G (p.Phe414Leu)
13g.113149424C>TCA485425036F10c.1374C>T (p.Phe458=)
c.*365C>T (n.*365C>T)
c.1242C>T (p.Phe414=)
COSMIC
13g.113149425C>ACA388794448F10c.1375C>A (p.Leu459Ile)
c.*366C>A (n.*366C>A)
c.1243C>A (p.Leu415Ile)
13g.113149425C=CA2120140747F10c.1375C= (p.Leu459=)
c.*366C= (n.*366C=)
c.1243C= (p.Leu415=)
13g.113149425C>GCA388794449F10c.1375C>G (p.Leu459Val)
c.*366C>G (n.*366C>G)
c.1243C>G (p.Leu415Val)
dbSNP gnomAD v2 gnomAD v4
13g.113149425C>TCA388794451F10c.1375C>T (p.Leu459Phe)
c.*366C>T (n.*366C>T)
c.1243C>T (p.Leu415Phe)
13g.113149426T>ACA388794454F10c.1376T>A (p.Leu459His)
c.*367T>A (n.*367T>A)
c.1244T>A (p.Leu415His)
13g.113149426T>CCA388794457F10c.1376T>C (p.Leu459Pro)
c.*367T>C (n.*367T>C)
c.1244T>C (p.Leu415Pro)
13g.113149426T>GCA388794455F10c.1376T>G (p.Leu459Arg)
c.*367T>G (n.*367T>G)
c.1244T>G (p.Leu415Arg)
13g.113149427C>ACA485425054F10c.1377C>A (p.Leu459=)
c.*368C>A (n.*368C>A)
c.1245C>A (p.Leu415=)
13g.113149427C=CA2120140752F10c.1377C= (p.Leu459=)
c.*368C= (n.*368C=)
c.1245C= (p.Leu415=)
13g.113149427C>GCA485425056F10c.1377C>G (p.Leu459=)
c.*368C>G (n.*368C>G)
c.1245C>G (p.Leu415=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.113149427C>TCA485425058F10c.1377C>T (p.Leu459=)
c.*368C>T (n.*368C>T)
c.1245C>T (p.Leu415=)
13g.113149428A>CCA388794459F10c.1378A>C (p.Lys460Gln)
c.*369A>C (n.*369A>C)
c.1246A>C (p.Lys416Gln)
gnomAD v4
13g.113149428A>GCA388794461F10c.1378A>G (p.Lys460Glu)
c.*369A>G (n.*369A>G)
c.1246A>G (p.Lys416Glu)
13g.113149428A>TCA388794462F10c.1378A>T (p.Lys460Ter)
c.*369A>T (n.*369A>T)
c.1246A>T (p.Lys416Ter)
13g.113149429A>CCA388794464F10c.1379A>C (p.Lys460Thr)
c.*370A>C (n.*370A>C)
c.1247A>C (p.Lys416Thr)
13g.113149429A>GCA388794465F10c.1379A>G (p.Lys460Arg)
c.*370A>G (n.*370A>G)
c.1247A>G (p.Lys416Arg)
13g.113149429A>TCA388794467F10c.1379A>T (p.Lys460Met)
c.*370A>T (n.*370A>T)
c.1247A>T (p.Lys416Met)
13g.113149429_113149430insACACACCCAACACACA2800665316F10c.1379_1380insACACACCCAACACA (p.Trp461HisfsTer11)
c.*370_*371insACACACCCAACACA (n.*370_*371insACACACCCAACACA)
c.1247_1248insACACACCCAACACA (p.Trp417HisfsTer11)
13g.113149430G>ACA485425074F10c.1380G>A (p.Lys460=)
c.*371G>A (n.*371G>A)
c.1248G>A (p.Lys416=)
13g.113149430G>CCA388794468F10c.1380G>C (p.Lys460Asn)
c.*371G>C (n.*371G>C)
c.1248G>C (p.Lys416Asn)
13g.113149430G>TCA388794470F10c.1380G>T (p.Lys460Asn)
c.*371G>T (n.*371G>T)
c.1248G>T (p.Lys416Asn)
13g.113149431T>ACA388794472F10c.1381T>A (p.Trp461Arg)
c.*372T>A (n.*372T>A)
c.1249T>A (p.Trp417Arg)
13g.113149431T>CCA388794474F10c.1381T>C (p.Trp461Arg)
c.*372T>C (n.*372T>C)
c.1249T>C (p.Trp417Arg)
dbSNP gnomAD v3 gnomAD v4
13g.113149431T>GCA388794475F10c.1381T>G (p.Trp461Gly)
c.*372T>G (n.*372T>G)
c.1249T>G (p.Trp417Gly)
13g.113149431T=CA2120140757F10c.1381T= (p.Trp461=)
c.*372T= (n.*372T=)
c.1249T= (p.Trp417=)
13g.113149432G>ACA388794477F10c.1382G>A (p.Trp461Ter)
c.*373G>A (n.*373G>A)
c.1250G>A (p.Trp417Ter)
13g.113149432G>CCA388794481F10c.1382G>C (p.Trp461Ser)
c.*373G>C (n.*373G>C)
c.1250G>C (p.Trp417Ser)
13g.113149432G>TCA388794479F10c.1382G>T (p.Trp461Leu)
c.*373G>T (n.*373G>T)
c.1250G>T (p.Trp417Leu)
13g.113149433G>ACA388794483F10c.1383G>A (p.Trp461Ter)
c.*374G>A (n.*374G>A)
c.1251G>A (p.Trp417Ter)
13g.113149433G>CCA388794486F10c.1383G>C (p.Trp461Cys)
c.*374G>C (n.*374G>C)
c.1251G>C (p.Trp417Cys)
gnomAD v4
13g.113149433G>TCA388794485F10c.1383G>T (p.Trp461Cys)
c.*374G>T (n.*374G>T)
c.1251G>T (p.Trp417Cys)
gnomAD v4
13g.113149434A>CCA388794488F10c.1384A>C (p.Ile462Leu)
c.*375A>C (n.*375A>C)
c.1252A>C (p.Ile418Leu)
13g.113149434A>GCA388794489F10c.1384A>G (p.Ile462Val)
c.*375A>G (n.*375A>G)
c.1252A>G (p.Ile418Val)
13g.113149434A>TCA388794490F10c.1384A>T (p.Ile462Phe)
c.*375A>T (n.*375A>T)
c.1252A>T (p.Ile418Phe)
13g.113149435T>ACA388794492F10c.1385T>A (p.Ile462Asn)
c.*376T>A (n.*376T>A)
c.1253T>A (p.Ile418Asn)
13g.113149435T>CCA388794493F10c.1385T>C (p.Ile462Thr)
c.*376T>C (n.*376T>C)
c.1253T>C (p.Ile418Thr)
13g.113149435T>GCA388794495F10c.1385T>G (p.Ile462Ser)
c.*376T>G (n.*376T>G)
c.1253T>G (p.Ile418Ser)
13g.113149436C>ACA485425111F10c.1386C>A (p.Ile462=)
c.*377C>A (n.*377C>A)
c.1254C>A (p.Ile418=)
13g.113149436C=CA2120140760F10c.1386C= (p.Ile462=)
c.*377C= (n.*377C=)
c.1254C= (p.Ile418=)
13g.113149436C>GCA388794497F10c.1386C>G (p.Ile462Met)
c.*377C>G (n.*377C>G)
c.1254C>G (p.Ile418Met)
13g.113149436C>TCA7060737F10c.1386C>T (p.Ile462=)
c.*377C>T (n.*377C>T)
c.1254C>T (p.Ile418=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.113149437G>ACA388794500F10c.1387G>A (p.Asp463Asn)
c.*378G>A (n.*378G>A)
c.1255G>A (p.Asp419Asn)
dbSNP gnomAD v4 COSMIC
13g.113149437G>CCA388794502F10c.1387G>C (p.Asp463His)
c.*378G>C (n.*378G>C)
c.1255G>C (p.Asp419His)
ClinVar dbSNP
13g.113149437G=CA2120140763F10c.1387G= (p.Asp463=)
c.*378G= (n.*378G=)
c.1255G= (p.Asp419=)
13g.113149437G>TCA388794504F10c.1387G>T (p.Asp463Tyr)
c.*378G>T (n.*378G>T)
c.1255G>T (p.Asp419Tyr)
gnomAD v4
13g.113149438A>CCA388794506F10c.1388A>C (p.Asp463Ala)
c.*379A>C (n.*379A>C)
c.1256A>C (p.Asp419Ala)
13g.113149438A>GCA388794509F10c.1388A>G (p.Asp463Gly)
c.*379A>G (n.*379A>G)
c.1256A>G (p.Asp419Gly)
13g.113149438A>TCA388794507F10c.1388A>T (p.Asp463Val)
c.*379A>T (n.*379A>T)
c.1256A>T (p.Asp419Val)
gnomAD v4
13g.113149439C>ACA388794510F10c.1389C>A (p.Asp463Glu)
c.*380C>A (n.*380C>A)
c.1257C>A (p.Asp419Glu)
COSMIC
13g.113149439C>GCA388794511F10c.1389C>G (p.Asp463Glu)
c.*380C>G (n.*380C>G)
c.1257C>G (p.Asp419Glu)
13g.113149439C>TCA485425138F10c.1389C>T (p.Asp463=)
c.*380C>T (n.*380C>T)
c.1257C>T (p.Asp419=)
13g.113149440A>CCA485425141F10c.1390A>C (p.Arg464=)
c.*381A>C (n.*381A>C)
c.1258A>C (p.Arg420=)
13g.113149440A>GCA388794513F10c.1390A>G (p.Arg464Gly)
c.*381A>G (n.*381A>G)
c.1258A>G (p.Arg420Gly)
13g.113149440A>TCA388794515F10c.1390A>T (p.Arg464Trp)
c.*381A>T (n.*381A>T)
c.1258A>T (p.Arg420Trp)
13g.113149441G>ACA388794516F10c.1391G>A (p.Arg464Lys)
c.*382G>A (n.*382G>A)
c.1259G>A (p.Arg420Lys)
13g.113149441G>CCA388794518F10c.1391G>C (p.Arg464Thr)
c.*382G>C (n.*382G>C)
c.1259G>C (p.Arg420Thr)
13g.113149441G>TCA388794520F10c.1391G>T (p.Arg464Met)
c.*382G>T (n.*382G>T)
c.1259G>T (p.Arg420Met)
13g.113149442G>ACA485425156F10c.1392G>A (p.Arg464=)
c.*383G>A (n.*383G>A)
c.1260G>A (p.Arg420=)
13g.113149442G>CCA388794521F10c.1392G>C (p.Arg464Ser)
c.*383G>C (n.*383G>C)
c.1260G>C (p.Arg420Ser)
13g.113149442G>TCA388794522F10c.1392G>T (p.Arg464Ser)
c.*383G>T (n.*383G>T)
c.1260G>T (p.Arg420Ser)
13g.113149443T>ACA388794526F10c.1393T>A (p.Ser465Thr)
c.*384T>A (n.*384T>A)
c.1261T>A (p.Ser421Thr)
13g.113149443T>CCA7060738F10c.1393T>C (p.Ser465Pro)
c.*384T>C (n.*384T>C)
c.1261T>C (p.Ser421Pro)
dbSNP ExAC gnomAD v2
13g.113149443T>GCA388794525F10c.1393T>G (p.Ser465Ala)
c.*384T>G (n.*384T>G)
c.1261T>G (p.Ser421Ala)
13g.113149443T=CA2120140768F10c.1393T= (p.Ser465=)
c.*384T= (n.*384T=)
c.1261T= (p.Ser421=)
13g.113149444C>ACA388794528F10c.1394C>A (p.Ser465Tyr)
c.*385C>A (n.*385C>A)
c.1262C>A (p.Ser421Tyr)
13g.113149444C>GCA388794529F10c.1394C>G (p.Ser465Cys)
c.*385C>G (n.*385C>G)
c.1262C>G (p.Ser421Cys)
13g.113149444C>TCA388794531F10c.1394C>T (p.Ser465Phe)
c.*385C>T (n.*385C>T)
c.1262C>T (p.Ser421Phe)
13g.113149445C>ACA485425181F10c.1395C>A (p.Ser465=)
c.*386C>A (n.*386C>A)
c.1263C>A (p.Ser421=)
13g.113149445C>GCA485425185F10c.1395C>G (p.Ser465=)
c.*386C>G (n.*386C>G)
c.1263C>G (p.Ser421=)
13g.113149445C>TCA485425184F10c.1395C>T (p.Ser465=)
c.*386C>T (n.*386C>T)
c.1263C>T (p.Ser421=)
COSMIC
13g.113149446A=CA2120140772F10c.1396A= (p.Met466=)
c.*387A= (n.*387A=)
c.1264A= (p.Met422=)
13g.113149446A>CCA388794533F10c.1396A>C (p.Met466Leu)
c.*387A>C (n.*387A>C)
c.1264A>C (p.Met422Leu)
13g.113149446A>GCA256478752F10c.1396A>G (p.Met466Val)
c.*387A>G (n.*387A>G)
c.1264A>G (p.Met422Val)
dbSNP gnomAD v4
13g.113149446A>TCA388794536F10c.1396A>T (p.Met466Leu)
c.*387A>T (n.*387A>T)
c.1264A>T (p.Met422Leu)
13g.113149447T>ACA388794537F10c.1397T>A (p.Met466Lys)
c.*388T>A (n.*388T>A)
c.1265T>A (p.Met422Lys)
13g.113149447T>CCA7060739F10c.1397T>C (p.Met466Thr)
c.*388T>C (n.*388T>C)
c.1265T>C (p.Met422Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.113149447T>GCA388794540F10c.1397T>G (p.Met466Arg)
c.*388T>G (n.*388T>G)
c.1265T>G (p.Met422Arg)
13g.113149447T=CA2120140779F10c.1397T= (p.Met466=)
c.*388T= (n.*388T=)
c.1265T= (p.Met422=)
13g.113149448G>ACA388794542F10c.1398G>A (p.Met466Ile)
c.*389G>A (n.*389G>A)
c.1266G>A (p.Met422Ile)
13g.113149448G>CCA388794543F10c.1398G>C (p.Met466Ile)
c.*389G>C (n.*389G>C)
c.1266G>C (p.Met422Ile)
13g.113149448G=CA2120140783F10c.1398G= (p.Met466=)
c.*389G= (n.*389G=)
c.1266G= (p.Met422=)
13g.113149448G>TCA388794545F10c.1398G>T (p.Met466Ile)
c.*389G>T (n.*389G>T)
c.1266G>T (p.Met422Ile)
13g.113149449A>CCA388794550F10c.1399A>C (p.Lys467Gln)
c.*390A>C (n.*390A>C)
c.1267A>C (p.Lys423Gln)
13g.113149449A>GCA388794547F10c.1399A>G (p.Lys467Glu)
c.*390A>G (n.*390A>G)
c.1267A>G (p.Lys423Glu)
13g.113149449A>TCA388794549F10c.1399A>T (p.Lys467Ter)
c.*390A>T (n.*390A>T)
c.1267A>T (p.Lys423Ter)
gnomAD v4
13g.113149452dupCA612868399F10c.1402dup (p.Thr468AsnfsTer?)
c.*393dup (n.*393dup)
c.1270dup (p.Thr424AsnfsTer?)
dbSNP gnomAD v2 gnomAD v4
13g.113149450A>CCA388794552F10c.1400A>C (p.Lys467Thr)
c.*391A>C (n.*391A>C)
c.1268A>C (p.Lys423Thr)
13g.113149450A>GCA388794554F10c.1400A>G (p.Lys467Arg)
c.*391A>G (n.*391A>G)
c.1268A>G (p.Lys423Arg)
13g.113149450A>TCA388794556F10c.1400A>T (p.Lys467Ile)
c.*391A>T (n.*391A>T)
c.1268A>T (p.Lys423Ile)
13g.113149451A>CCA388794558F10c.1401A>C (p.Lys467Asn)
c.*392A>C (n.*392A>C)
c.1269A>C (p.Lys423Asn)
13g.113149451A>GCA485425225F10c.1401A>G (p.Lys467=)
c.*392A>G (n.*392A>G)
c.1269A>G (p.Lys423=)
13g.113149451A>TCA388794559F10c.1401A>T (p.Lys467Asn)
c.*392A>T (n.*392A>T)
c.1269A>T (p.Lys423Asn)
13g.113149452A=CA2120140787F10c.1402A= (p.Thr468=)
c.*393A= (n.*393A=)
c.1270A= (p.Thr424=)
13g.113149452A>CCA7060740F10c.1402A>C (p.Thr468Pro)
c.*393A>C (n.*393A>C)
c.1270A>C (p.Thr424Pro)
dbSNP ExAC gnomAD v2
13g.113149452A>GCA388794562F10c.1402A>G (p.Thr468Ala)
c.*393A>G (n.*393A>G)
c.1270A>G (p.Thr424Ala)
13g.113149452A>TCA388794563F10c.1402A>T (p.Thr468Ser)
c.*393A>T (n.*393A>T)
c.1270A>T (p.Thr424Ser)
13g.113149453C>ACA388794566F10c.1403C>A (p.Thr468Asn)
c.*394C>A (n.*394C>A)
c.1271C>A (p.Thr424Asn)
13g.113149453C=CA2120140804F10c.1403C= (p.Thr468=)
c.*394C= (n.*394C=)
c.1271C= (p.Thr424=)
13g.113149453C>GCA388794567F10c.1403C>G (p.Thr468Ser)
c.*394C>G (n.*394C>G)
c.1271C>G (p.Thr424Ser)
dbSNP
13g.113149453C>TCA388794569F10c.1403C>T (p.Thr468Ile)
c.*394C>T (n.*394C>T)
c.1271C>T (p.Thr424Ile)
dbSNP gnomAD v4
13g.113149456_113149480delCA2623810410F10c.1406_1430del (p.Arg469MetfsTer6)
c.*397_*421del (n.*397_*421del)
c.1274_1298del (p.Arg425MetfsTer6)
gnomAD v4
13g.113149454C>ACA485425244F10c.1404C>A (p.Thr468=)
c.*395C>A (n.*395C>A)
c.1272C>A (p.Thr424=)
13g.113149454C=CA2120140809F10c.1404C= (p.Thr468=)
c.*395C= (n.*395C=)
c.1272C= (p.Thr424=)
13g.113149454C>GCA485425246F10c.1404C>G (p.Thr468=)
c.*395C>G (n.*395C>G)
c.1272C>G (p.Thr424=)
13g.113149454C>TCA485425247F10c.1404C>T (p.Thr468=)
c.*395C>T (n.*395C>T)
c.1272C>T (p.Thr424=)
dbSNP gnomAD v3 gnomAD v4
13g.113149455A>CCA485425249F10c.1405A>C (p.Arg469=)
c.*396A>C (n.*396A>C)
c.1273A>C (p.Arg425=)
13g.113149455A>GCA388794571F10c.1405A>G (p.Arg469Gly)
c.*396A>G (n.*396A>G)
c.1273A>G (p.Arg425Gly)
13g.113149455A>TCA388794572F10c.1405A>T (p.Arg469Trp)
c.*396A>T (n.*396A>T)
c.1273A>T (p.Arg425Trp)
13g.113149456G>ACA7060741F10c.1406G>A (p.Arg469Lys)
c.*397G>A (n.*397G>A)
c.1274G>A (p.Arg425Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149456G>CCA388794577F10c.1406G>C (p.Arg469Thr)
c.*397G>C (n.*397G>C)
c.1274G>C (p.Arg425Thr)
13g.113149456G=CA2120140816F10c.1406G= (p.Arg469=)
c.*397G= (n.*397G=)
c.1274G= (p.Arg425=)
13g.113149456G>TCA388794575F10c.1406G>T (p.Arg469Met)
c.*397G>T (n.*397G>T)
c.1274G>T (p.Arg425Met)
13g.113149459delCA2623810415F10c.1409del (p.Gly470AlafsTer13)
c.*400del (n.*400del)
c.1277del (p.Gly426AlafsTer13)
gnomAD v4
13g.113149457G>ACA485425263F10c.1407G>A (p.Arg469=)
c.*398G>A (n.*398G>A)
c.1275G>A (p.Arg425=)
13g.113149457G>CCA388794581F10c.1407G>C (p.Arg469Ser)
c.*398G>C (n.*398G>C)
c.1275G>C (p.Arg425Ser)
13g.113149457G>TCA388794579F10c.1407G>T (p.Arg469Ser)
c.*398G>T (n.*398G>T)
c.1275G>T (p.Arg425Ser)
gnomAD v4
13g.113149458G>ACA7060742F10c.1408G>A (p.Gly470Ser)
c.*399G>A (n.*399G>A)
c.1276G>A (p.Gly426Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149458G>CCA7060743F10c.1408G>C (p.Gly470Arg)
c.*399G>C (n.*399G>C)
c.1276G>C (p.Gly426Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149458G=CA2120140822F10c.1408G= (p.Gly470=)
c.*399G= (n.*399G=)
c.1276G= (p.Gly426=)
13g.113149458G>TCA388794584F10c.1408G>T (p.Gly470Cys)
c.*399G>T (n.*399G>T)
c.1276G>T (p.Gly426Cys)
13g.113149459G>ACA388794586F10c.1409G>A (p.Gly470Asp)
c.*400G>A (n.*400G>A)
c.1277G>A (p.Gly426Asp)
dbSNP
13g.113149459G>CCA388794588F10c.1409G>C (p.Gly470Ala)
c.*400G>C (n.*400G>C)
c.1277G>C (p.Gly426Ala)
13g.113149459G=CA2120140832F10c.1409G= (p.Gly470=)
c.*400G= (n.*400G=)
c.1277G= (p.Gly426=)
13g.113149459G>TCA388794590F10c.1409G>T (p.Gly470Val)
c.*400G>T (n.*400G>T)
c.1277G>T (p.Gly426Val)
dbSNP
13g.113149460C>ACA485425289F10c.1410C>A (p.Gly470=)
c.*401C>A (n.*401C>A)
c.1278C>A (p.Gly426=)
13g.113149460C=CA2120140837F10c.1410C= (p.Gly470=)
c.*401C= (n.*401C=)
c.1278C= (p.Gly426=)
13g.113149460C>GCA485425294F10c.1410C>G (p.Gly470=)
c.*401C>G (n.*401C>G)
c.1278C>G (p.Gly426=)
13g.113149460C>TCA485425290F10c.1410C>T (p.Gly470=)
c.*401C>T (n.*401C>T)
c.1278C>T (p.Gly426=)
dbSNP gnomAD v2 gnomAD v4
13g.113149461T>ACA388794592F10c.1411T>A (p.Leu471Met)
c.*402T>A (n.*402T>A)
c.1279T>A (p.Leu427Met)
13g.113149461T>CCA485425298F10c.1411T>C (p.Leu471=)
c.*402T>C (n.*402T>C)
c.1279T>C (p.Leu427=)
13g.113149461T>GCA388794593F10c.1411T>G (p.Leu471Val)
c.*402T>G (n.*402T>G)
c.1279T>G (p.Leu427Val)
13g.113149462T>ACA388794596F10c.1412T>A (p.Leu471Ter)
c.*403T>A (n.*403T>A)
c.1280T>A (p.Leu427Ter)
13g.113149462T>CCA388794598F10c.1412T>C (p.Leu471Ser)
c.*403T>C (n.*403T>C)
c.1280T>C (p.Leu427Ser)
13g.113149462T>GCA388794600F10c.1412T>G (p.Leu471Trp)
c.*403T>G (n.*403T>G)
c.1280T>G (p.Leu427Trp)
13g.113149463G>ACA485425308F10c.1413G>A (p.Leu471=)
c.*404G>A (n.*404G>A)
c.1281G>A (p.Leu427=)
gnomAD v4
13g.113149463G>CCA388794602F10c.1413G>C (p.Leu471Phe)
c.*404G>C (n.*404G>C)
c.1281G>C (p.Leu427Phe)
13g.113149463G>TCA388794603F10c.1413G>T (p.Leu471Phe)
c.*404G>T (n.*404G>T)
c.1281G>T (p.Leu427Phe)
13g.113149464C>ACA388794607F10c.1414C>A (p.Pro472Thr)
c.*405C>A (n.*405C>A)
c.1282C>A (p.Pro428Thr)
13g.113149464C>GCA388794604F10c.1414C>G (p.Pro472Ala)
c.*405C>G (n.*405C>G)
c.1282C>G (p.Pro428Ala)
13g.113149464C>TCA388794605F10c.1414C>T (p.Pro472Ser)
c.*405C>T (n.*405C>T)
c.1282C>T (p.Pro428Ser)
13g.113149465C>ACA388794608F10c.1415C>A (p.Pro472His)
c.*406C>A (n.*406C>A)
c.1283C>A (p.Pro428His)
13g.113149465C=CA2120140842F10c.1415C= (p.Pro472=)
c.*406C= (n.*406C=)
c.1283C= (p.Pro428=)
13g.113149465C>GCA388794610F10c.1415C>G (p.Pro472Arg)
c.*406C>G (n.*406C>G)
c.1283C>G (p.Pro428Arg)
13g.113149465C>TCA388794611F10c.1415C>T (p.Pro472Leu)
c.*406C>T (n.*406C>T)
c.1283C>T (p.Pro428Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched