Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.113149367_113149376del | CA2623810142 | F10 | c.1317_1326del (p.Trp439CysfsTer25) c.*308_*317del (n.*308_*317del) c.1185_1194del (p.Trp395CysfsTer25) | gnomAD v4 |
13 | g.113149368_113149376del | CA2800665256 | F10 | c.1318_1326del (p.Gly440_Gly442del) c.*309_*317del (n.*309_*317del) c.1186_1194del (p.Gly396_Gly398del) | |
13 | g.113149370A>C | CA485424188 | F10 | c.1320A>C (p.Gly440=) c.*311A>C (n.*311A>C) c.1188A>C (p.Gly396=) | |
13 | g.113149370A>G | CA485424191 | F10 | c.1320A>G (p.Gly440=) c.*311A>G (n.*311A>G) c.1188A>G (p.Gly396=) | |
13 | g.113149370A>T | CA485424189 | F10 | c.1320A>T (p.Gly440=) c.*311A>T (n.*311A>T) c.1188A>T (p.Gly396=) | |
13 | g.113149370_113149376del | CA2623810182 | F10 | c.1320_1326del (p.Glu441ValfsTer24) c.*311_*317del (n.*311_*317del) c.1188_1194del (p.Glu397ValfsTer24) | gnomAD v4 |
13 | g.113149370_113149371insTTTTTTTTTAAT | CA2800665269 | F10 | c.1320_1321insTTTTTTTTTAAT (p.Gly440_Glu441insPhePhePheAsn) c.*311_*312insTTTTTTTTTAAT (n.*311_*312insTTTTTTTTTAAT) c.1188_1189insTTTTTTTTTAAT (p.Gly396_Glu397insPhePhePheAsn) | |
13 | g.113149371G>A | CA388794242 | F10 | c.1321G>A (p.Glu441Lys) c.*312G>A (n.*312G>A) c.1189G>A (p.Glu397Lys) | ClinVar dbSNP |
13 | g.113149371G>C | CA388794243 | F10 | c.1321G>C (p.Glu441Gln) c.*312G>C (n.*312G>C) c.1189G>C (p.Glu397Gln) | |
13 | g.113149371G= | CA2120140562 | F10 | c.1321G= (p.Glu441=) c.*312G= (n.*312G=) c.1189G= (p.Glu397=) | |
13 | g.113149371G>T | CA388794245 | F10 | c.1321G>T (p.Glu441Ter) c.*312G>T (n.*312G>T) c.1189G>T (p.Glu397Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149372A>C | CA388794247 | F10 | c.1322A>C (p.Glu441Ala) c.*313A>C (n.*313A>C) c.1190A>C (p.Glu397Ala) | |
13 | g.113149372A>G | CA388794251 | F10 | c.1322A>G (p.Glu441Gly) c.*313A>G (n.*313A>G) c.1190A>G (p.Glu397Gly) | |
13 | g.113149372A>T | CA388794249 | F10 | c.1322A>T (p.Glu441Val) c.*313A>T (n.*313A>T) c.1190A>T (p.Glu397Val) | |
13 | g.113149372_113149376delinsAGGGC | CA2120140568 | F10 | c.1322_1326delinsAGGGC (p.Glu441=) c.*313_*317delinsAGGGC (n.*313_*317delinsAGGGC) c.1190_1194delinsAGGGC (p.Glu397=) | |
13 | g.113149373G>A | CA485424195 | F10 | c.1323G>A (p.Glu441=) c.*314G>A (n.*314G>A) c.1191G>A (p.Glu397=) | dbSNP gnomAD v4 |
13 | g.113149373G>C | CA388794253 | F10 | c.1323G>C (p.Glu441Asp) c.*314G>C (n.*314G>C) c.1191G>C (p.Glu397Asp) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149373G= | CA2120140578 | F10 | c.1323G= (p.Glu441=) c.*314G= (n.*314G=) c.1191G= (p.Glu397=) | |
13 | g.113149373G>T | CA388794254 | F10 | c.1323G>T (p.Glu441Asp) c.*314G>T (n.*314G>T) c.1191G>T (p.Glu397Asp) | |
13 | g.113149373_113149375del | CA2800665271 | F10 | c.1323_1325del (p.Glu441_Gly442delinsAsp) c.*314_*316del (n.*314_*316del) c.1191_1193del (p.Glu397_Gly398delinsAsp) | |
13 | g.113149375del | CA2623810190 | F10 | c.1325del (p.Gly442AlafsTer25) c.*316del (n.*316del) c.1193del (p.Gly398AlafsTer25) | gnomAD v4 |
13 | g.113149373_113149376del | CA612868378 | F10 | c.1323_1326del (p.Glu441AspfsTer25) c.*314_*317del (n.*314_*317del) c.1191_1194del (p.Glu397AspfsTer25) | dbSNP gnomAD v2 |
13 | g.113149373_113149376delinsGGGC | CA2120140572 | F10 | c.1323_1326delinsGGGC (p.Glu441=) c.*314_*317delinsGGGC (n.*314_*317delinsGGGC) c.1191_1194delinsGGGC (p.Glu397=) | |
13 | g.113149373_113149384del | CA612868377 | F10 | c.1323_1334del (p.Glu441_Arg445delinsAsp) c.*314_*325del (n.*314_*325del) c.1191_1202del (p.Glu397_Arg401delinsAsp) | gnomAD v2 gnomAD v4 |
13 | g.113149373_113149374insTTTTTTAATCATAC | CA960419792 | F10 | c.1323_1324insTTTTTTAATCATAC (p.Gly442PhefsTer30) c.*314_*315insTTTTTTAATCATAC (n.*314_*315insTTTTTTAATCATAC) c.1191_1192insTTTTTTAATCATAC (p.Gly398PhefsTer30) | gnomAD v3 gnomAD v4 |
13 | g.113149374G>A | CA388794257 | F10 | c.1324G>A (p.Gly442Ser) c.*315G>A (n.*315G>A) c.1192G>A (p.Gly398Ser) | gnomAD v4 |
13 | g.113149374G>C | CA388794258 | F10 | c.1324G>C (p.Gly442Arg) c.*315G>C (n.*315G>C) c.1192G>C (p.Gly398Arg) | |
13 | g.113149374G= | CA2120140580 | F10 | c.1324G= (p.Gly442=) c.*315G= (n.*315G=) c.1192G= (p.Gly398=) | |
13 | g.113149374G>T | CA388794259 | F10 | c.1324G>T (p.Gly442Cys) c.*315G>T (n.*315G>T) c.1192G>T (p.Gly398Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149374_113149376del | CA612868379 | F10 | c.1324_1326del (p.Gly442del) c.*315_*317del (n.*315_*317del) c.1192_1194del (p.Gly398del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149375G>A | CA388794263 | F10 | c.1325G>A (p.Gly442Asp) c.*316G>A (n.*316G>A) c.1193G>A (p.Gly398Asp) | ClinVar dbSNP gnomAD v4 |
13 | g.113149375G>C | CA388794264 | F10 | c.1325G>C (p.Gly442Ala) c.*316G>C (n.*316G>C) c.1193G>C (p.Gly398Ala) | |
13 | g.113149375G= | CA2120140585 | F10 | c.1325G= (p.Gly442=) c.*316G= (n.*316G=) c.1193G= (p.Gly398=) | |
13 | g.113149375G>T | CA388794261 | F10 | c.1325G>T (p.Gly442Val) c.*316G>T (n.*316G>T) c.1193G>T (p.Gly398Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149375_113149376del | CA960419801 | F10 | c.1325_1326del (p.Gly442ValfsTer4) c.*316_*317del (n.*316_*317del) c.1193_1194del (p.Gly398ValfsTer4) | gnomAD v3 gnomAD v4 |
13 | g.113149376del | CA2623810225 | F10 | c.1326del (p.Cys443ValfsTer24) c.*317del (n.*317del) c.1194del (p.Cys399ValfsTer24) | gnomAD v4 |
13 | g.113149376C>A | CA485424198 | F10 | c.1326C>A (p.Gly442=) c.*317C>A (n.*317C>A) c.1194C>A (p.Gly398=) | |
13 | g.113149376C= | CA2120140595 | F10 | c.1326C= (p.Gly442=) c.*317C= (n.*317C=) c.1194C= (p.Gly398=) | |
13 | g.113149376C>G | CA7060729 | F10 | c.1326C>G (p.Gly442=) c.*317C>G (n.*317C>G) c.1194C>G (p.Gly398=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149376C>T | CA485424200 | F10 | c.1326C>T (p.Gly442=) c.*317C>T (n.*317C>T) c.1194C>T (p.Gly398=) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149377T>A | CA388794268 | F10 | c.1327T>A (p.Cys443Ser) c.*318T>A (n.*318T>A) c.1195T>A (p.Cys399Ser) | |
13 | g.113149377T>C | CA388794269 | F10 | c.1327T>C (p.Cys443Arg) c.*318T>C (n.*318T>C) c.1195T>C (p.Cys399Arg) | |
13 | g.113149377T>G | CA388794271 | F10 | c.1327T>G (p.Cys443Gly) c.*318T>G (n.*318T>G) c.1195T>G (p.Cys399Gly) | |
13 | g.113149377_113149378insTTT | CA2800665279 | F10 | c.1327_1328insTTT (p.Gly442_Cys443insPhe) c.*318_*319insTTT (n.*318_*319insTTT) c.1195_1196insTTT (p.Gly398_Cys399insPhe) | |
13 | g.113149377_113149379del | CA612868380 | F10 | c.1327_1329del (p.Cys443del) c.*318_*320del (n.*318_*320del) c.1195_1197del (p.Cys399del) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149378del | CA960419809 | F10 | c.1328del (p.Cys443LeufsTer24) c.*319del (n.*319del) c.1196del (p.Cys399LeufsTer24) | gnomAD v3 gnomAD v4 |
13 | g.113149378G>A | CA388794273 | F10 | c.1328G>A (p.Cys443Tyr) c.*319G>A (n.*319G>A) c.1196G>A (p.Cys399Tyr) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149378G>C | CA388794274 | F10 | c.1328G>C (p.Cys443Ser) c.*319G>C (n.*319G>C) c.1196G>C (p.Cys399Ser) | gnomAD v4 |
13 | g.113149378G= | CA2120140602 | F10 | c.1328G= (p.Cys443=) c.*319G= (n.*319G=) c.1196G= (p.Cys399=) | |
13 | g.113149378G>T | CA388794276 | F10 | c.1328G>T (p.Cys443Phe) c.*319G>T (n.*319G>T) c.1196G>T (p.Cys399Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149380_113149385del | CA2623810233 | F10 | c.1330_1335del (p.Ala444_Arg445del) c.*321_*326del (n.*321_*326del) c.1198_1203del (p.Ala400_Arg401del) | gnomAD v4 |
13 | g.113149379T>A | CA388794278 | F10 | c.1329T>A (p.Cys443Ter) c.*320T>A (n.*320T>A) c.1197T>A (p.Cys399Ter) | |
13 | g.113149379T>C | CA485424735 | F10 | c.1329T>C (p.Cys443=) c.*320T>C (n.*320T>C) c.1197T>C (p.Cys399=) | |
13 | g.113149379T>G | CA388794280 | F10 | c.1329T>G (p.Cys443Trp) c.*320T>G (n.*320T>G) c.1197T>G (p.Cys399Trp) | |
13 | g.113149379_113149383del | CA2623810235 | F10 | c.1329_1333del (p.Cys443TrpfsTer2) c.*320_*324del (n.*320_*324del) c.1197_1201del (p.Cys399TrpfsTer2) | gnomAD v4 |
13 | g.113149379_113149384delinsTGCCCG | CA2120140609 | F10 | c.1329_1334delinsTGCCCG (p.Cys443=) c.*320_*325delinsTGCCCG (n.*320_*325delinsTGCCCG) c.1197_1202delinsTGCCCG (p.Cys399=) | |
13 | g.113149380G>A | CA388794281 | F10 | c.1330G>A (p.Ala444Thr) c.*321G>A (n.*321G>A) c.1198G>A (p.Ala400Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149380G>C | CA388794282 | F10 | c.1330G>C (p.Ala444Pro) c.*321G>C (n.*321G>C) c.1198G>C (p.Ala400Pro) | |
13 | g.113149380G= | CA2120140615 | F10 | c.1330G= (p.Ala444=) c.*321G= (n.*321G=) c.1198G= (p.Ala400=) | |
13 | g.113149380G>T | CA388794283 | F10 | c.1330G>T (p.Ala444Ser) c.*321G>T (n.*321G>T) c.1198G>T (p.Ala400Ser) | |
13 | g.113149380_113149382del | CA2623810242 | F10 | c.1330_1332del (p.Ala444del) c.*321_*323del (n.*321_*323del) c.1198_1200del (p.Ala400del) | gnomAD v4 |
13 | g.113149380_113149384del | CA612868383 | F10 | c.1330_1334del (p.Ala444Ter) c.*321_*325del (n.*321_*325del) c.1198_1202del (p.Ala400Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149381_113149384del | CA612868384 | F10 | c.1331_1334del (p.Ala444ValfsTer22) c.*322_*325del (n.*322_*325del) c.1199_1202del (p.Ala400ValfsTer22) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149381_113149391del | CA612868382 | F10 | c.1331_1341del (p.Ala444GlufsTer?) c.*322_*332del (n.*322_*332del) c.1199_1209del (p.Ala400GlufsTer?) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149381C>A | CA388794285 | F10 | c.1331C>A (p.Ala444Asp) c.*322C>A (n.*322C>A) c.1199C>A (p.Ala400Asp) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149381C= | CA2120140622 | F10 | c.1331C= (p.Ala444=) c.*322C= (n.*322C=) c.1199C= (p.Ala400=) | |
13 | g.113149381C>G | CA388794287 | F10 | c.1331C>G (p.Ala444Gly) c.*322C>G (n.*322C>G) c.1199C>G (p.Ala400Gly) | |
13 | g.113149381C>T | CA388794288 | F10 | c.1331C>T (p.Ala444Val) c.*322C>T (n.*322C>T) c.1199C>T (p.Ala400Val) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149381_113149383del | CA2800665283 | F10 | c.1331_1333del (p.Ala444_Arg445delinsGly) c.*322_*324del (n.*322_*324del) c.1199_1201del (p.Ala400_Arg401delinsGly) | |
13 | g.113149382C>A | CA485424753 | F10 | c.1332C>A (p.Ala444=) c.*323C>A (n.*323C>A) c.1200C>A (p.Ala400=) | |
13 | g.113149382C>G | CA485424755 | F10 | c.1332C>G (p.Ala444=) c.*323C>G (n.*323C>G) c.1200C>G (p.Ala400=) | gnomAD v4 |
13 | g.113149382C>T | CA485424757 | F10 | c.1332C>T (p.Ala444=) c.*323C>T (n.*323C>T) c.1200C>T (p.Ala400=) | |
13 | g.113149382_113149384del | CA612868385 | F10 | c.1332_1334del (p.Arg445del) c.*323_*325del (n.*323_*325del) c.1200_1202del (p.Arg401del) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149383C>A | CA388794290 | F10 | c.1333C>A (p.Arg445Ser) c.*324C>A (n.*324C>A) c.1201C>A (p.Arg401Ser) | gnomAD v4 |
13 | g.113149383C= | CA2120140628 | F10 | c.1333C= (p.Arg445=) c.*324C= (n.*324C=) c.1201C= (p.Arg401=) | |
13 | g.113149383C>G | CA388794291 | F10 | c.1333C>G (p.Arg445Gly) c.*324C>G (n.*324C>G) c.1201C>G (p.Arg401Gly) | gnomAD v4 |
13 | g.113149383C>T | CA7060730 | F10 | c.1333C>T (p.Arg445Cys) c.*324C>T (n.*324C>T) c.1201C>T (p.Arg401Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
13 | g.113149384G>A | CA388794293 | F10 | c.1334G>A (p.Arg445His) c.*325G>A (n.*325G>A) c.1202G>A (p.Arg401His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149384G>C | CA388794295 | F10 | c.1334G>C (p.Arg445Pro) c.*325G>C (n.*325G>C) c.1202G>C (p.Arg401Pro) | |
13 | g.113149384G= | CA2120140635 | F10 | c.1334G= (p.Arg445=) c.*325G= (n.*325G=) c.1202G= (p.Arg401=) | |
13 | g.113149384G>T | CA388794296 | F10 | c.1334G>T (p.Arg445Leu) c.*325G>T (n.*325G>T) c.1202G>T (p.Arg401Leu) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149384_113149395del | CA612868386 | F10 | c.1334_1345del (p.Arg445_Tyr449delinsHis) c.*325_*336del (n.*325_*336del) c.1202_1213del (p.Arg401_Tyr405delinsHis) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149384_113149385insATGA | CA2800665289 | F10 | c.1334_1335insATGA (p.Lys446Ter) c.*325_*326insATGA (n.*325_*326insATGA) c.1202_1203insATGA (p.Lys402Ter) | |
13 | g.113149385T>A | CA485424774 | F10 | c.1335T>A (p.Arg445=) c.*326T>A (n.*326T>A) c.1203T>A (p.Arg401=) | |
13 | g.113149385T>C | CA485424778 | F10 | c.1335T>C (p.Arg445=) c.*326T>C (n.*326T>C) c.1203T>C (p.Arg401=) | dbSNP |
13 | g.113149385T>G | CA485424779 | F10 | c.1335T>G (p.Arg445=) c.*326T>G (n.*326T>G) c.1203T>G (p.Arg401=) | gnomAD v4 |
13 | g.113149385T= | CA2120140641 | F10 | c.1335T= (p.Arg445=) c.*326T= (n.*326T=) c.1203T= (p.Arg401=) | |
13 | g.113149385_113149386insTT | CA612868387 | F10 | c.1335_1336insTT (p.Lys446LeufsTer22) c.*326_*327insTT (n.*326_*327insTT) c.1203_1204insTT (p.Lys402LeufsTer22) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149385_113149386insTTT | CA612868388 | F10 | c.1335_1336insTTT (p.Arg445_Lys446insPhe) c.*326_*327insTTT (n.*326_*327insTTT) c.1203_1204insTTT (p.Arg401_Lys402insPhe) | gnomAD v2 |
13 | g.113149385_113149386insTTTTT | CA2623810275 | F10 | c.1335_1336insTTTTT (p.Lys446PhefsTer23) c.*326_*327insTTTTT (n.*326_*327insTTTTT) c.1203_1204insTTTTT (p.Lys402PhefsTer23) | gnomAD v4 |
13 | g.113149385_113149386insTGTTTT | CA2800665290 | F10 | c.1335_1336insTGTTTT (p.Arg445_Lys446insCysPhe) c.*326_*327insTGTTTT (n.*326_*327insTGTTTT) c.1203_1204insTGTTTT (p.Arg401_Lys402insCysPhe) | |
13 | g.113149385_113149386insTTTTTTTTT | CA612868389 | F10 | c.1335_1336insTTTTTTTTT (p.Arg445_Lys446insPhePhePhe) c.*326_*327insTTTTTTTTT (n.*326_*327insTTTTTTTTT) c.1203_1204insTTTTTTTTT (p.Arg401_Lys402insPhePhePhe) | gnomAD v2 |
13 | g.113149385_113149390delinsTAAGGG | CA2120140639 | F10 | c.1335_1340delinsTAAGGG (p.Arg445=) c.*326_*331delinsTAAGGG (n.*326_*331delinsTAAGGG) c.1203_1208delinsTAAGGG (p.Arg401=) | |
13 | g.113149386A>C | CA388794299 | F10 | c.1336A>C (p.Lys446Gln) c.*327A>C (n.*327A>C) c.1204A>C (p.Lys402Gln) | |
13 | g.113149386A>G | CA388794301 | F10 | c.1336A>G (p.Lys446Glu) c.*327A>G (n.*327A>G) c.1204A>G (p.Lys402Glu) | |
13 | g.113149386A>T | CA388794303 | F10 | c.1336A>T (p.Lys446Ter) c.*327A>T (n.*327A>T) c.1204A>T (p.Lys402Ter) | |
13 | g.113149386_113149390del | CA612868390 | F10 | c.1336_1340del (p.Lys446GlufsTer?) c.*327_*331del (n.*327_*331del) c.1204_1208del (p.Lys402GlufsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149387A>C | CA388794305 | F10 | c.1337A>C (p.Lys446Thr) c.*328A>C (n.*328A>C) c.1205A>C (p.Lys402Thr) | gnomAD v2 gnomAD v4 COSMIC |
13 | g.113149387A>G | CA388794307 | F10 | c.1337A>G (p.Lys446Arg) c.*328A>G (n.*328A>G) c.1205A>G (p.Lys402Arg) | |
13 | g.113149387A>T | CA388794308 | F10 | c.1337A>T (p.Lys446Met) c.*328A>T (n.*328A>T) c.1205A>T (p.Lys402Met) | gnomAD v4 |
13 | g.113149387_113149389delinsAGG | CA2120140645 | F10 | c.1337_1339delinsAGG (p.Lys446=) c.*328_*330delinsAGG (n.*328_*330delinsAGG) c.1205_1207delinsAGG (p.Lys402=) | |
13 | g.113149387_113149388insTCATAC | CA2800665298 | F10 | c.1337_1338insTCATAC (p.Lys446delinsAsnHisThr) c.*328_*329insTCATAC (n.*328_*329insTCATAC) c.1205_1206insTCATAC (p.Lys402delinsAsnHisThr) | |
13 | g.113149387_113149388insTGATAC | CA2623810294 | F10 | c.1337_1338insTGATAC (p.Lys446delinsAsnAspThr) c.*328_*329insTGATAC (n.*328_*329insTGATAC) c.1205_1206insTGATAC (p.Lys402delinsAsnAspThr) | gnomAD v4 |
13 | g.113149388G>A | CA7060731 | F10 | c.1338G>A (p.Lys446=) c.*329G>A (n.*329G>A) c.1206G>A (p.Lys402=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149388G>C | CA388794311 | F10 | c.1338G>C (p.Lys446Asn) c.*329G>C (n.*329G>C) c.1206G>C (p.Lys402Asn) | |
13 | g.113149388G= | CA2120140649 | F10 | c.1338G= (p.Lys446=) c.*329G= (n.*329G=) c.1206G= (p.Lys402=) | |
13 | g.113149388G>T | CA388794313 | F10 | c.1338G>T (p.Lys446Asn) c.*329G>T (n.*329G>T) c.1206G>T (p.Lys402Asn) | gnomAD v4 |
13 | g.113149390_113149391del | CA612868391 | F10 | c.1340_1341del (p.Gly447GlufsTer?) c.*331_*332del (n.*331_*332del) c.1208_1209del (p.Gly403GlufsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149389G>A | CA7060732 | F10 | c.1339G>A (p.Gly447Arg) c.*330G>A (n.*330G>A) c.1207G>A (p.Gly403Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.113149389G>C | CA388794317 | F10 | c.1339G>C (p.Gly447Arg) c.*330G>C (n.*330G>C) c.1207G>C (p.Gly403Arg) | |
13 | g.113149389G= | CA2120140650 | F10 | c.1339G= (p.Gly447=) c.*330G= (n.*330G=) c.1207G= (p.Gly403=) | |
13 | g.113149389G>T | CA388794315 | F10 | c.1339G>T (p.Gly447Trp) c.*330G>T (n.*330G>T) c.1207G>T (p.Gly403Trp) | |
13 | g.113149390G>A | CA388794319 | F10 | c.1340G>A (p.Gly447Glu) c.*331G>A (n.*331G>A) c.1208G>A (p.Gly403Glu) | |
13 | g.113149390G>C | CA388794320 | F10 | c.1340G>C (p.Gly447Ala) c.*331G>C (n.*331G>C) c.1208G>C (p.Gly403Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149390G= | CA2120140653 | F10 | c.1340G= (p.Gly447=) c.*331G= (n.*331G=) c.1208G= (p.Gly403=) | |
13 | g.113149390G>T | CA388794322 | F10 | c.1340G>T (p.Gly447Val) c.*331G>T (n.*331G>T) c.1208G>T (p.Gly403Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149391_113149394del | CA2623810313 | F10 | c.1341_1344del (p.Lys448ThrfsTer18) c.*332_*335del (n.*332_*335del) c.1209_1212del (p.Lys404ThrfsTer18) | gnomAD v4 |
13 | g.113149391G>A | CA256478746 | F10 | c.1341G>A (p.Gly447=) c.*332G>A (n.*332G>A) c.1209G>A (p.Gly403=) | dbSNP |
13 | g.113149391G>C | CA485424819 | F10 | c.1341G>C (p.Gly447=) c.*332G>C (n.*332G>C) c.1209G>C (p.Gly403=) | |
13 | g.113149391G= | CA2120140658 | F10 | c.1341G= (p.Gly447=) c.*332G= (n.*332G=) c.1209G= (p.Gly403=) | |
13 | g.113149391G>T | CA485424823 | F10 | c.1341G>T (p.Gly447=) c.*332G>T (n.*332G>T) c.1209G>T (p.Gly403=) | |
13 | g.113149392A>C | CA388794324 | F10 | c.1342A>C (p.Lys448Gln) c.*333A>C (n.*333A>C) c.1210A>C (p.Lys404Gln) | |
13 | g.113149392A>G | CA388794326 | F10 | c.1342A>G (p.Lys448Glu) c.*333A>G (n.*333A>G) c.1210A>G (p.Lys404Glu) | |
13 | g.113149392A>T | CA388794327 | F10 | c.1342A>T (p.Lys448Ter) c.*333A>T (n.*333A>T) c.1210A>T (p.Lys404Ter) | |
13 | g.113149392_113149394delinsAAG | CA2120140661 | F10 | c.1342_1344delinsAAG (p.Lys448=) c.*333_*335delinsAAG (n.*333_*335delinsAAG) c.1210_1212delinsAAG (p.Lys404=) | |
13 | g.113149392_113149393insCC | CA612868393 | F10 | c.1342_1343insCC (p.Lys448ThrfsTer20) c.*333_*334insCC (n.*333_*334insCC) c.1210_1211insCC (p.Lys404ThrfsTer20) | gnomAD v2 gnomAD v4 |
13 | g.113149393A>C | CA388794332 | F10 | c.1343A>C (p.Lys448Thr) c.*334A>C (n.*334A>C) c.1211A>C (p.Lys404Thr) | gnomAD v4 |
13 | g.113149393A>G | CA388794329 | F10 | c.1343A>G (p.Lys448Arg) c.*334A>G (n.*334A>G) c.1211A>G (p.Lys404Arg) | |
13 | g.113149393A>T | CA388794331 | F10 | c.1343A>T (p.Lys448Met) c.*334A>T (n.*334A>T) c.1211A>T (p.Lys404Met) | gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149393_113149394del | CA612868392 | F10 | c.1343_1344del (p.Lys448IlefsTer?) c.*334_*335del (n.*334_*335del) c.1211_1212del (p.Lys404IlefsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149394G>A | CA485424838 | F10 | c.1344G>A (p.Lys448=) c.*335G>A (n.*335G>A) c.1212G>A (p.Lys404=) | |
13 | g.113149394G>C | CA388794334 | F10 | c.1344G>C (p.Lys448Asn) c.*335G>C (n.*335G>C) c.1212G>C (p.Lys404Asn) | gnomAD v4 |
13 | g.113149394G= | CA2120140667 | F10 | c.1344G= (p.Lys448=) c.*335G= (n.*335G=) c.1212G= (p.Lys404=) | |
13 | g.113149394G>T | CA388794336 | F10 | c.1344G>T (p.Lys448Asn) c.*335G>T (n.*335G>T) c.1212G>T (p.Lys404Asn) | |
13 | g.113149394_113149395del | CA612868394 | F10 | c.1344_1345del (p.Tyr449ArgfsTer?) c.*335_*336del (n.*335_*336del) c.1212_1213del (p.Tyr405ArgfsTer?) | gnomAD v2 gnomAD v4 |
13 | g.113149394_113149395insA | CA612868395 | F10 | c.1344_1345insA (p.Tyr449IlefsTer?) c.*335_*336insA (n.*335_*336insA) c.1212_1213insA (p.Tyr405IlefsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149395T>A | CA388794338 | F10 | c.1345T>A (p.Tyr449Asn) c.*336T>A (n.*336T>A) c.1213T>A (p.Tyr405Asn) | gnomAD v4 |
13 | g.113149395T>C | CA388794339 | F10 | c.1345T>C (p.Tyr449His) c.*336T>C (n.*336T>C) c.1213T>C (p.Tyr405His) | |
13 | g.113149395T>G | CA388794342 | F10 | c.1345T>G (p.Tyr449Asp) c.*336T>G (n.*336T>G) c.1213T>G (p.Tyr405Asp) | |
13 | g.113149396A= | CA2120140669 | F10 | c.1346A= (p.Tyr449=) c.*337A= (n.*337A=) c.1214A= (p.Tyr405=) | |
13 | g.113149396A>C | CA388794344 | F10 | c.1346A>C (p.Tyr449Ser) c.*337A>C (n.*337A>C) c.1214A>C (p.Tyr405Ser) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.113149396A>G | CA388794347 | F10 | c.1346A>G (p.Tyr449Cys) c.*337A>G (n.*337A>G) c.1214A>G (p.Tyr405Cys) | |
13 | g.113149396A>T | CA388794345 | F10 | c.1346A>T (p.Tyr449Phe) c.*337A>T (n.*337A>T) c.1214A>T (p.Tyr405Phe) | |
13 | g.113149397C>A | CA388794349 | F10 | c.1347C>A (p.Tyr449Ter) c.*338C>A (n.*338C>A) c.1215C>A (p.Tyr405Ter) | |
13 | g.113149397C= | CA2120140673 | F10 | c.1347C= (p.Tyr449=) c.*338C= (n.*338C=) c.1215C= (p.Tyr405=) | |
13 | g.113149397C>G | CA388794351 | F10 | c.1347C>G (p.Tyr449Ter) c.*338C>G (n.*338C>G) c.1215C>G (p.Tyr405Ter) | |
13 | g.113149397C>T | CA485424857 | F10 | c.1347C>T (p.Tyr449=) c.*338C>T (n.*338C>T) c.1215C>T (p.Tyr405=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149397dup | CA612868396 | F10 | c.1347dup (p.Gly450ArgfsTer?) c.*338dup (n.*338dup) c.1215dup (p.Gly406ArgfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149398G>A | CA388794353 | F10 | c.1348G>A (p.Gly450Arg) c.*339G>A (n.*339G>A) c.1216G>A (p.Gly406Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
13 | g.113149398G>C | CA388794355 | F10 | c.1348G>C (p.Gly450Arg) c.*339G>C (n.*339G>C) c.1216G>C (p.Gly406Arg) | |
13 | g.113149398G= | CA2120140680 | F10 | c.1348G= (p.Gly450=) c.*339G= (n.*339G=) c.1216G= (p.Gly406=) | |
13 | g.113149398G>T | CA388794356 | F10 | c.1348G>T (p.Gly450Trp) c.*339G>T (n.*339G>T) c.1216G>T (p.Gly406Trp) | |
13 | g.113149399G>A | CA388794357 | F10 | c.1349G>A (p.Gly450Glu) c.*340G>A (n.*340G>A) c.1217G>A (p.Gly406Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149399G>C | CA388794358 | F10 | c.1349G>C (p.Gly450Ala) c.*340G>C (n.*340G>C) c.1217G>C (p.Gly406Ala) | |
13 | g.113149399G= | CA2120140688 | F10 | c.1349G= (p.Gly450=) c.*340G= (n.*340G=) c.1217G= (p.Gly406=) | |
13 | g.113149399G>T | CA388794359 | F10 | c.1349G>T (p.Gly450Val) c.*340G>T (n.*340G>T) c.1217G>T (p.Gly406Val) | dbSNP gnomAD v2 |
13 | g.113149399_113149400insCGAACACCGA | CA2623810349 | F10 | c.1349_1350insCGAACACCGA (p.Ile451GlufsTer?) c.*340_*341insCGAACACCGA (n.*340_*341insCGAACACCGA) c.1217_1218insCGAACACCGA (p.Ile407GlufsTer?) | gnomAD v4 |
13 | g.113149399_113149400insCGACCACCGA | CA612868397 | F10 | c.1349_1350insCGACCACCGA (p.Ile451AspfsTer?) c.*340_*341insCGACCACCGA (n.*340_*341insCGACCACCGA) c.1217_1218insCGACCACCGA (p.Ile407AspfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149399_113149400insCGACCTCCGA | CA2623810347 | F10 | c.1349_1350insCGACCTCCGA (p.Ile451AspfsTer?) c.*340_*341insCGACCTCCGA (n.*340_*341insCGACCTCCGA) c.1217_1218insCGACCTCCGA (p.Ile407AspfsTer?) | gnomAD v4 |
13 | g.113149399_113149400insCGACGACCGA | CA2800665312 | F10 | c.1349_1350insCGACGACCGA (p.Ile451AspfsTer?) c.*340_*341insCGACGACCGA (n.*340_*341insCGACGACCGA) c.1217_1218insCGACGACCGA (p.Ile407AspfsTer?) | |
13 | g.113149400G>A | CA7060733 | F10 | c.1350G>A (p.Gly450=) c.*341G>A (n.*341G>A) c.1218G>A (p.Gly406=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149400G>C | CA485424862 | F10 | c.1350G>C (p.Gly450=) c.*341G>C (n.*341G>C) c.1218G>C (p.Gly406=) | gnomAD v4 |
13 | g.113149400G= | CA2120140693 | F10 | c.1350G= (p.Gly450=) c.*341G= (n.*341G=) c.1218G= (p.Gly406=) | |
13 | g.113149400G>T | CA485424864 | F10 | c.1350G>T (p.Gly450=) c.*341G>T (n.*341G>T) c.1218G>T (p.Gly406=) | |
13 | g.113149401A= | CA2120140696 | F10 | c.1351A= (p.Ile451=) c.*342A= (n.*342A=) c.1219A= (p.Ile407=) | |
13 | g.113149401A>C | CA7060734 | F10 | c.1351A>C (p.Ile451Leu) c.*342A>C (n.*342A>C) c.1219A>C (p.Ile407Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149401A>G | CA388794363 | F10 | c.1351A>G (p.Ile451Val) c.*342A>G (n.*342A>G) c.1219A>G (p.Ile407Val) | |
13 | g.113149401A>T | CA388794364 | F10 | c.1351A>T (p.Ile451Phe) c.*342A>T (n.*342A>T) c.1219A>T (p.Ile407Phe) | |
13 | g.113149402T>A | CA388794369 | F10 | c.1352T>A (p.Ile451Asn) c.*343T>A (n.*343T>A) c.1220T>A (p.Ile407Asn) | |
13 | g.113149402T>C | CA388794370 | F10 | c.1352T>C (p.Ile451Thr) c.*343T>C (n.*343T>C) c.1220T>C (p.Ile407Thr) | |
13 | g.113149402T>G | CA388794367 | F10 | c.1352T>G (p.Ile451Ser) c.*343T>G (n.*343T>G) c.1220T>G (p.Ile407Ser) | |
13 | g.113149403C>A | CA485424878 | F10 | c.1353C>A (p.Ile451=) c.*344C>A (n.*344C>A) c.1221C>A (p.Ile407=) | |
13 | g.113149403C>G | CA388794372 | F10 | c.1353C>G (p.Ile451Met) c.*344C>G (n.*344C>G) c.1221C>G (p.Ile407Met) | |
13 | g.113149403C>T | CA485424882 | F10 | c.1353C>T (p.Ile451=) c.*344C>T (n.*344C>T) c.1221C>T (p.Ile407=) | |
13 | g.113149404T>A | CA388794375 | F10 | c.1354T>A (p.Tyr452Asn) c.*345T>A (n.*345T>A) c.1222T>A (p.Tyr408Asn) | |
13 | g.113149404T>C | CA388794374 | F10 | c.1354T>C (p.Tyr452His) c.*345T>C (n.*345T>C) c.1222T>C (p.Tyr408His) | |
13 | g.113149404T>G | CA388794377 | F10 | c.1354T>G (p.Tyr452Asp) c.*345T>G (n.*345T>G) c.1222T>G (p.Tyr408Asp) | |
13 | g.113149404_113149418delinsTACACCAAGGTCACC | CA2120140698 | F10 | c.1354_1368delinsTACACCAAGGTCACC (p.Tyr452=) c.*345_*359delinsTACACCAAGGTCACC (n.*345_*359delinsTACACCAAGGTCACC) c.1222_1236delinsTACACCAAGGTCACC (p.Tyr408=) | |
13 | g.113149405A>C | CA388794378 | F10 | c.1355A>C (p.Tyr452Ser) c.*346A>C (n.*346A>C) c.1223A>C (p.Tyr408Ser) | |
13 | g.113149405A>G | CA388794382 | F10 | c.1355A>G (p.Tyr452Cys) c.*346A>G (n.*346A>G) c.1223A>G (p.Tyr408Cys) | |
13 | g.113149405A>T | CA388794380 | F10 | c.1355A>T (p.Tyr452Phe) c.*346A>T (n.*346A>T) c.1223A>T (p.Tyr408Phe) | |
13 | g.113149405_113149418del | CA2120140701 | F10 | c.1355_1368del (p.Tyr452CysfsTer?) c.*346_*359del (n.*346_*359del) c.1223_1236del (p.Tyr408CysfsTer?) | dbSNP |
13 | g.113149406C>A | CA388794384 | F10 | c.1356C>A (p.Tyr452Ter) c.*347C>A (n.*347C>A) c.1224C>A (p.Tyr408Ter) | |
13 | g.113149406C>G | CA388794385 | F10 | c.1356C>G (p.Tyr452Ter) c.*347C>G (n.*347C>G) c.1224C>G (p.Tyr408Ter) | |
13 | g.113149406C>T | CA485424900 | F10 | c.1356C>T (p.Tyr452=) c.*347C>T (n.*347C>T) c.1224C>T (p.Tyr408=) | gnomAD v4 |
13 | g.113149407A>C | CA388794387 | F10 | c.1357A>C (p.Thr453Pro) c.*348A>C (n.*348A>C) c.1225A>C (p.Thr409Pro) | |
13 | g.113149407A>G | CA388794388 | F10 | c.1357A>G (p.Thr453Ala) c.*348A>G (n.*348A>G) c.1225A>G (p.Thr409Ala) | |
13 | g.113149407A>T | CA388794389 | F10 | c.1357A>T (p.Thr453Ser) c.*348A>T (n.*348A>T) c.1225A>T (p.Thr409Ser) | |
13 | g.113149408C>A | CA388794391 | F10 | c.1358C>A (p.Thr453Asn) c.*349C>A (n.*349C>A) c.1226C>A (p.Thr409Asn) | |
13 | g.113149408C= | CA2120140705 | F10 | c.1358C= (p.Thr453=) c.*349C= (n.*349C=) c.1226C= (p.Thr409=) | |
13 | g.113149408C>G | CA256478749 | F10 | c.1358C>G (p.Thr453Ser) c.*349C>G (n.*349C>G) c.1226C>G (p.Thr409Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149408C>T | CA388794393 | F10 | c.1358C>T (p.Thr453Ile) c.*349C>T (n.*349C>T) c.1226C>T (p.Thr409Ile) | dbSNP |
13 | g.113149409C>A | CA485424917 | F10 | c.1359C>A (p.Thr453=) c.*350C>A (n.*350C>A) c.1227C>A (p.Thr409=) | |
13 | g.113149409C= | CA2120140708 | F10 | c.1359C= (p.Thr453=) c.*350C= (n.*350C=) c.1227C= (p.Thr409=) | |
13 | g.113149409C>G | CA485424919 | F10 | c.1359C>G (p.Thr453=) c.*350C>G (n.*350C>G) c.1227C>G (p.Thr409=) | gnomAD v4 |
13 | g.113149409C>T | CA485424922 | F10 | c.1359C>T (p.Thr453=) c.*350C>T (n.*350C>T) c.1227C>T (p.Thr409=) | dbSNP |
13 | g.113149410A= | CA2120140713 | F10 | c.1360A= (p.Lys454=) c.*351A= (n.*351A=) c.1228A= (p.Lys410=) | |
13 | g.113149410A>C | CA388794394 | F10 | c.1360A>C (p.Lys454Gln) c.*351A>C (n.*351A>C) c.1228A>C (p.Lys410Gln) | |
13 | g.113149410A>G | CA388794395 | F10 | c.1360A>G (p.Lys454Glu) c.*351A>G (n.*351A>G) c.1228A>G (p.Lys410Glu) | gnomAD v4 |
13 | g.113149410A>T | CA388794396 | F10 | c.1360A>T (p.Lys454Ter) c.*351A>T (n.*351A>T) c.1228A>T (p.Lys410Ter) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149411A>C | CA388794397 | F10 | c.1361A>C (p.Lys454Thr) c.*352A>C (n.*352A>C) c.1229A>C (p.Lys410Thr) | |
13 | g.113149411A>G | CA388794398 | F10 | c.1361A>G (p.Lys454Arg) c.*352A>G (n.*352A>G) c.1229A>G (p.Lys410Arg) | |
13 | g.113149411A>T | CA388794399 | F10 | c.1361A>T (p.Lys454Met) c.*352A>T (n.*352A>T) c.1229A>T (p.Lys410Met) | |
13 | g.113149411_113149412insCACACCCAACACA | CA2800665314 | F10 | c.1361_1362insCACACCCAACACA (p.Lys454AsnfsTer?) c.*352_*353insCACACCCAACACA (n.*352_*353insCACACCCAACACA) c.1229_1230insCACACCCAACACA (p.Lys410AsnfsTer?) | |
13 | g.113149412G>A | CA485424940 | F10 | c.1362G>A (p.Lys454=) c.*353G>A (n.*353G>A) c.1230G>A (p.Lys410=) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149412G>C | CA388794403 | F10 | c.1362G>C (p.Lys454Asn) c.*353G>C (n.*353G>C) c.1230G>C (p.Lys410Asn) | gnomAD v4 |
13 | g.113149412G= | CA2120140716 | F10 | c.1362G= (p.Lys454=) c.*353G= (n.*353G=) c.1230G= (p.Lys410=) | |
13 | g.113149412G>T | CA388794401 | F10 | c.1362G>T (p.Lys454Asn) c.*353G>T (n.*353G>T) c.1230G>T (p.Lys410Asn) | |
13 | g.113149413G>A | CA388794404 | F10 | c.1363G>A (p.Val455Ile) c.*354G>A (n.*354G>A) c.1231G>A (p.Val411Ile) | dbSNP |
13 | g.113149413G>C | CA388794406 | F10 | c.1363G>C (p.Val455Leu) c.*354G>C (n.*354G>C) c.1231G>C (p.Val411Leu) | |
13 | g.113149413G= | CA2120140720 | F10 | c.1363G= (p.Val455=) c.*354G= (n.*354G=) c.1231G= (p.Val411=) | |
13 | g.113149413G>T | CA388794408 | F10 | c.1363G>T (p.Val455Phe) c.*354G>T (n.*354G>T) c.1231G>T (p.Val411Phe) | |
13 | g.113149414T>A | CA388794410 | F10 | c.1364T>A (p.Val455Asp) c.*355T>A (n.*355T>A) c.1232T>A (p.Val411Asp) | |
13 | g.113149414T>C | CA388794411 | F10 | c.1364T>C (p.Val455Ala) c.*355T>C (n.*355T>C) c.1232T>C (p.Val411Ala) | dbSNP gnomAD v4 |
13 | g.113149414T>G | CA388794413 | F10 | c.1364T>G (p.Val455Gly) c.*355T>G (n.*355T>G) c.1232T>G (p.Val411Gly) | |
13 | g.113149414T= | CA2120140724 | F10 | c.1364T= (p.Val455=) c.*355T= (n.*355T=) c.1232T= (p.Val411=) | |
13 | g.113149415C>A | CA485424962 | F10 | c.1365C>A (p.Val455=) c.*356C>A (n.*356C>A) c.1233C>A (p.Val411=) | |
13 | g.113149415C>G | CA485424964 | F10 | c.1365C>G (p.Val455=) c.*356C>G (n.*356C>G) c.1233C>G (p.Val411=) | |
13 | g.113149415C>T | CA485424968 | F10 | c.1365C>T (p.Val455=) c.*356C>T (n.*356C>T) c.1233C>T (p.Val411=) | gnomAD v4 |
13 | g.113149416A>C | CA388794415 | F10 | c.1366A>C (p.Thr456Pro) c.*357A>C (n.*357A>C) c.1234A>C (p.Thr412Pro) | |
13 | g.113149416A>G | CA388794417 | F10 | c.1366A>G (p.Thr456Ala) c.*357A>G (n.*357A>G) c.1234A>G (p.Thr412Ala) | |
13 | g.113149416A>T | CA388794418 | F10 | c.1366A>T (p.Thr456Ser) c.*357A>T (n.*357A>T) c.1234A>T (p.Thr412Ser) | |
13 | g.113149417C>A | CA388794420 | F10 | c.1367C>A (p.Thr456Asn) c.*358C>A (n.*358C>A) c.1235C>A (p.Thr412Asn) | |
13 | g.113149417C= | CA2120140730 | F10 | c.1367C= (p.Thr456=) c.*358C= (n.*358C=) c.1235C= (p.Thr412=) | |
13 | g.113149417C>G | CA388794422 | F10 | c.1367C>G (p.Thr456Ser) c.*358C>G (n.*358C>G) c.1235C>G (p.Thr412Ser) | |
13 | g.113149417C>T | CA388794423 | F10 | c.1367C>T (p.Thr456Ile) c.*358C>T (n.*358C>T) c.1235C>T (p.Thr412Ile) | dbSNP |
13 | g.113149418C>A | CA485424985 | F10 | c.1368C>A (p.Thr456=) c.*359C>A (n.*359C>A) c.1236C>A (p.Thr412=) | |
13 | g.113149418C= | CA2120140736 | F10 | c.1368C= (p.Thr456=) c.*359C= (n.*359C=) c.1236C= (p.Thr412=) | |
13 | g.113149418C>G | CA485424989 | F10 | c.1368C>G (p.Thr456=) c.*359C>G (n.*359C>G) c.1236C>G (p.Thr412=) | gnomAD v4 |
13 | g.113149418C>T | CA7060735 | F10 | c.1368C>T (p.Thr456=) c.*359C>T (n.*359C>T) c.1236C>T (p.Thr412=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
13 | g.113149419G>A | CA7060736 | F10 | c.1369G>A (p.Ala457Thr) c.*360G>A (n.*360G>A) c.1237G>A (p.Ala413Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149419G>C | CA388794424 | F10 | c.1369G>C (p.Ala457Pro) c.*360G>C (n.*360G>C) c.1237G>C (p.Ala413Pro) | |
13 | g.113149419G= | CA2120140738 | F10 | c.1369G= (p.Ala457=) c.*360G= (n.*360G=) c.1237G= (p.Ala413=) | |
13 | g.113149419G>T | CA388794426 | F10 | c.1369G>T (p.Ala457Ser) c.*360G>T (n.*360G>T) c.1237G>T (p.Ala413Ser) | dbSNP |
13 | g.113149420C>A | CA388794428 | F10 | c.1370C>A (p.Ala457Asp) c.*361C>A (n.*361C>A) c.1238C>A (p.Ala413Asp) | |
13 | g.113149420C>G | CA388794430 | F10 | c.1370C>G (p.Ala457Gly) c.*361C>G (n.*361C>G) c.1238C>G (p.Ala413Gly) | |
13 | g.113149420C>T | CA388794431 | F10 | c.1370C>T (p.Ala457Val) c.*361C>T (n.*361C>T) c.1238C>T (p.Ala413Val) | gnomAD v4 |
13 | g.113149421C>A | CA485425005 | F10 | c.1371C>A (p.Ala457=) c.*362C>A (n.*362C>A) c.1239C>A (p.Ala413=) | |
13 | g.113149421C= | CA2120140741 | F10 | c.1371C= (p.Ala457=) c.*362C= (n.*362C=) c.1239C= (p.Ala413=) | |
13 | g.113149421C>G | CA485425007 | F10 | c.1371C>G (p.Ala457=) c.*362C>G (n.*362C>G) c.1239C>G (p.Ala413=) | |
13 | g.113149421C>T | CA485425010 | F10 | c.1371C>T (p.Ala457=) c.*362C>T (n.*362C>T) c.1239C>T (p.Ala413=) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149422T>A | CA388794434 | F10 | c.1372T>A (p.Phe458Ile) c.*363T>A (n.*363T>A) c.1240T>A (p.Phe414Ile) | |
13 | g.113149422T>C | CA388794436 | F10 | c.1372T>C (p.Phe458Leu) c.*363T>C (n.*363T>C) c.1240T>C (p.Phe414Leu) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149422T>G | CA388794437 | F10 | c.1372T>G (p.Phe458Val) c.*363T>G (n.*363T>G) c.1240T>G (p.Phe414Val) | |
13 | g.113149422T= | CA2120140744 | F10 | c.1372T= (p.Phe458=) c.*363T= (n.*363T=) c.1240T= (p.Phe414=) | |
13 | g.113149423T>A | CA388794442 | F10 | c.1373T>A (p.Phe458Tyr) c.*364T>A (n.*364T>A) c.1241T>A (p.Phe414Tyr) | |
13 | g.113149423T>C | CA388794439 | F10 | c.1373T>C (p.Phe458Ser) c.*364T>C (n.*364T>C) c.1241T>C (p.Phe414Ser) | |
13 | g.113149423T>G | CA388794441 | F10 | c.1373T>G (p.Phe458Cys) c.*364T>G (n.*364T>G) c.1241T>G (p.Phe414Cys) | |
13 | g.113149424C>A | CA388794444 | F10 | c.1374C>A (p.Phe458Leu) c.*365C>A (n.*365C>A) c.1242C>A (p.Phe414Leu) | |
13 | g.113149424C>G | CA388794446 | F10 | c.1374C>G (p.Phe458Leu) c.*365C>G (n.*365C>G) c.1242C>G (p.Phe414Leu) | |
13 | g.113149424C>T | CA485425036 | F10 | c.1374C>T (p.Phe458=) c.*365C>T (n.*365C>T) c.1242C>T (p.Phe414=) | COSMIC |
13 | g.113149425C>A | CA388794448 | F10 | c.1375C>A (p.Leu459Ile) c.*366C>A (n.*366C>A) c.1243C>A (p.Leu415Ile) | |
13 | g.113149425C= | CA2120140747 | F10 | c.1375C= (p.Leu459=) c.*366C= (n.*366C=) c.1243C= (p.Leu415=) | |
13 | g.113149425C>G | CA388794449 | F10 | c.1375C>G (p.Leu459Val) c.*366C>G (n.*366C>G) c.1243C>G (p.Leu415Val) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.113149425C>T | CA388794451 | F10 | c.1375C>T (p.Leu459Phe) c.*366C>T (n.*366C>T) c.1243C>T (p.Leu415Phe) | |
13 | g.113149426T>A | CA388794454 | F10 | c.1376T>A (p.Leu459His) c.*367T>A (n.*367T>A) c.1244T>A (p.Leu415His) | |
13 | g.113149426T>C | CA388794457 | F10 | c.1376T>C (p.Leu459Pro) c.*367T>C (n.*367T>C) c.1244T>C (p.Leu415Pro) | |
13 | g.113149426T>G | CA388794455 | F10 | c.1376T>G (p.Leu459Arg) c.*367T>G (n.*367T>G) c.1244T>G (p.Leu415Arg) | |
13 | g.113149427C>A | CA485425054 | F10 | c.1377C>A (p.Leu459=) c.*368C>A (n.*368C>A) c.1245C>A (p.Leu415=) | |
13 | g.113149427C= | CA2120140752 | F10 | c.1377C= (p.Leu459=) c.*368C= (n.*368C=) c.1245C= (p.Leu415=) | |
13 | g.113149427C>G | CA485425056 | F10 | c.1377C>G (p.Leu459=) c.*368C>G (n.*368C>G) c.1245C>G (p.Leu415=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149427C>T | CA485425058 | F10 | c.1377C>T (p.Leu459=) c.*368C>T (n.*368C>T) c.1245C>T (p.Leu415=) | |
13 | g.113149428A>C | CA388794459 | F10 | c.1378A>C (p.Lys460Gln) c.*369A>C (n.*369A>C) c.1246A>C (p.Lys416Gln) | gnomAD v4 |
13 | g.113149428A>G | CA388794461 | F10 | c.1378A>G (p.Lys460Glu) c.*369A>G (n.*369A>G) c.1246A>G (p.Lys416Glu) | |
13 | g.113149428A>T | CA388794462 | F10 | c.1378A>T (p.Lys460Ter) c.*369A>T (n.*369A>T) c.1246A>T (p.Lys416Ter) | |
13 | g.113149429A>C | CA388794464 | F10 | c.1379A>C (p.Lys460Thr) c.*370A>C (n.*370A>C) c.1247A>C (p.Lys416Thr) | |
13 | g.113149429A>G | CA388794465 | F10 | c.1379A>G (p.Lys460Arg) c.*370A>G (n.*370A>G) c.1247A>G (p.Lys416Arg) | |
13 | g.113149429A>T | CA388794467 | F10 | c.1379A>T (p.Lys460Met) c.*370A>T (n.*370A>T) c.1247A>T (p.Lys416Met) | |
13 | g.113149429_113149430insACACACCCAACACA | CA2800665316 | F10 | c.1379_1380insACACACCCAACACA (p.Trp461HisfsTer11) c.*370_*371insACACACCCAACACA (n.*370_*371insACACACCCAACACA) c.1247_1248insACACACCCAACACA (p.Trp417HisfsTer11) | |
13 | g.113149430G>A | CA485425074 | F10 | c.1380G>A (p.Lys460=) c.*371G>A (n.*371G>A) c.1248G>A (p.Lys416=) | |
13 | g.113149430G>C | CA388794468 | F10 | c.1380G>C (p.Lys460Asn) c.*371G>C (n.*371G>C) c.1248G>C (p.Lys416Asn) | |
13 | g.113149430G>T | CA388794470 | F10 | c.1380G>T (p.Lys460Asn) c.*371G>T (n.*371G>T) c.1248G>T (p.Lys416Asn) | |
13 | g.113149431T>A | CA388794472 | F10 | c.1381T>A (p.Trp461Arg) c.*372T>A (n.*372T>A) c.1249T>A (p.Trp417Arg) | |
13 | g.113149431T>C | CA388794474 | F10 | c.1381T>C (p.Trp461Arg) c.*372T>C (n.*372T>C) c.1249T>C (p.Trp417Arg) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149431T>G | CA388794475 | F10 | c.1381T>G (p.Trp461Gly) c.*372T>G (n.*372T>G) c.1249T>G (p.Trp417Gly) | |
13 | g.113149431T= | CA2120140757 | F10 | c.1381T= (p.Trp461=) c.*372T= (n.*372T=) c.1249T= (p.Trp417=) | |
13 | g.113149432G>A | CA388794477 | F10 | c.1382G>A (p.Trp461Ter) c.*373G>A (n.*373G>A) c.1250G>A (p.Trp417Ter) | |
13 | g.113149432G>C | CA388794481 | F10 | c.1382G>C (p.Trp461Ser) c.*373G>C (n.*373G>C) c.1250G>C (p.Trp417Ser) | |
13 | g.113149432G>T | CA388794479 | F10 | c.1382G>T (p.Trp461Leu) c.*373G>T (n.*373G>T) c.1250G>T (p.Trp417Leu) | |
13 | g.113149433G>A | CA388794483 | F10 | c.1383G>A (p.Trp461Ter) c.*374G>A (n.*374G>A) c.1251G>A (p.Trp417Ter) | |
13 | g.113149433G>C | CA388794486 | F10 | c.1383G>C (p.Trp461Cys) c.*374G>C (n.*374G>C) c.1251G>C (p.Trp417Cys) | gnomAD v4 |
13 | g.113149433G>T | CA388794485 | F10 | c.1383G>T (p.Trp461Cys) c.*374G>T (n.*374G>T) c.1251G>T (p.Trp417Cys) | gnomAD v4 |
13 | g.113149434A>C | CA388794488 | F10 | c.1384A>C (p.Ile462Leu) c.*375A>C (n.*375A>C) c.1252A>C (p.Ile418Leu) | |
13 | g.113149434A>G | CA388794489 | F10 | c.1384A>G (p.Ile462Val) c.*375A>G (n.*375A>G) c.1252A>G (p.Ile418Val) | |
13 | g.113149434A>T | CA388794490 | F10 | c.1384A>T (p.Ile462Phe) c.*375A>T (n.*375A>T) c.1252A>T (p.Ile418Phe) | |
13 | g.113149435T>A | CA388794492 | F10 | c.1385T>A (p.Ile462Asn) c.*376T>A (n.*376T>A) c.1253T>A (p.Ile418Asn) | |
13 | g.113149435T>C | CA388794493 | F10 | c.1385T>C (p.Ile462Thr) c.*376T>C (n.*376T>C) c.1253T>C (p.Ile418Thr) | |
13 | g.113149435T>G | CA388794495 | F10 | c.1385T>G (p.Ile462Ser) c.*376T>G (n.*376T>G) c.1253T>G (p.Ile418Ser) | |
13 | g.113149436C>A | CA485425111 | F10 | c.1386C>A (p.Ile462=) c.*377C>A (n.*377C>A) c.1254C>A (p.Ile418=) | |
13 | g.113149436C= | CA2120140760 | F10 | c.1386C= (p.Ile462=) c.*377C= (n.*377C=) c.1254C= (p.Ile418=) | |
13 | g.113149436C>G | CA388794497 | F10 | c.1386C>G (p.Ile462Met) c.*377C>G (n.*377C>G) c.1254C>G (p.Ile418Met) | |
13 | g.113149436C>T | CA7060737 | F10 | c.1386C>T (p.Ile462=) c.*377C>T (n.*377C>T) c.1254C>T (p.Ile418=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
13 | g.113149437G>A | CA388794500 | F10 | c.1387G>A (p.Asp463Asn) c.*378G>A (n.*378G>A) c.1255G>A (p.Asp419Asn) | dbSNP gnomAD v4 COSMIC |
13 | g.113149437G>C | CA388794502 | F10 | c.1387G>C (p.Asp463His) c.*378G>C (n.*378G>C) c.1255G>C (p.Asp419His) | ClinVar dbSNP |
13 | g.113149437G= | CA2120140763 | F10 | c.1387G= (p.Asp463=) c.*378G= (n.*378G=) c.1255G= (p.Asp419=) | |
13 | g.113149437G>T | CA388794504 | F10 | c.1387G>T (p.Asp463Tyr) c.*378G>T (n.*378G>T) c.1255G>T (p.Asp419Tyr) | gnomAD v4 |
13 | g.113149438A>C | CA388794506 | F10 | c.1388A>C (p.Asp463Ala) c.*379A>C (n.*379A>C) c.1256A>C (p.Asp419Ala) | |
13 | g.113149438A>G | CA388794509 | F10 | c.1388A>G (p.Asp463Gly) c.*379A>G (n.*379A>G) c.1256A>G (p.Asp419Gly) | |
13 | g.113149438A>T | CA388794507 | F10 | c.1388A>T (p.Asp463Val) c.*379A>T (n.*379A>T) c.1256A>T (p.Asp419Val) | gnomAD v4 |
13 | g.113149439C>A | CA388794510 | F10 | c.1389C>A (p.Asp463Glu) c.*380C>A (n.*380C>A) c.1257C>A (p.Asp419Glu) | COSMIC |
13 | g.113149439C>G | CA388794511 | F10 | c.1389C>G (p.Asp463Glu) c.*380C>G (n.*380C>G) c.1257C>G (p.Asp419Glu) | |
13 | g.113149439C>T | CA485425138 | F10 | c.1389C>T (p.Asp463=) c.*380C>T (n.*380C>T) c.1257C>T (p.Asp419=) | |
13 | g.113149440A>C | CA485425141 | F10 | c.1390A>C (p.Arg464=) c.*381A>C (n.*381A>C) c.1258A>C (p.Arg420=) | |
13 | g.113149440A>G | CA388794513 | F10 | c.1390A>G (p.Arg464Gly) c.*381A>G (n.*381A>G) c.1258A>G (p.Arg420Gly) | |
13 | g.113149440A>T | CA388794515 | F10 | c.1390A>T (p.Arg464Trp) c.*381A>T (n.*381A>T) c.1258A>T (p.Arg420Trp) | |
13 | g.113149441G>A | CA388794516 | F10 | c.1391G>A (p.Arg464Lys) c.*382G>A (n.*382G>A) c.1259G>A (p.Arg420Lys) | |
13 | g.113149441G>C | CA388794518 | F10 | c.1391G>C (p.Arg464Thr) c.*382G>C (n.*382G>C) c.1259G>C (p.Arg420Thr) | |
13 | g.113149441G>T | CA388794520 | F10 | c.1391G>T (p.Arg464Met) c.*382G>T (n.*382G>T) c.1259G>T (p.Arg420Met) | |
13 | g.113149442G>A | CA485425156 | F10 | c.1392G>A (p.Arg464=) c.*383G>A (n.*383G>A) c.1260G>A (p.Arg420=) | |
13 | g.113149442G>C | CA388794521 | F10 | c.1392G>C (p.Arg464Ser) c.*383G>C (n.*383G>C) c.1260G>C (p.Arg420Ser) | |
13 | g.113149442G>T | CA388794522 | F10 | c.1392G>T (p.Arg464Ser) c.*383G>T (n.*383G>T) c.1260G>T (p.Arg420Ser) | |
13 | g.113149443T>A | CA388794526 | F10 | c.1393T>A (p.Ser465Thr) c.*384T>A (n.*384T>A) c.1261T>A (p.Ser421Thr) | |
13 | g.113149443T>C | CA7060738 | F10 | c.1393T>C (p.Ser465Pro) c.*384T>C (n.*384T>C) c.1261T>C (p.Ser421Pro) | dbSNP ExAC gnomAD v2 |
13 | g.113149443T>G | CA388794525 | F10 | c.1393T>G (p.Ser465Ala) c.*384T>G (n.*384T>G) c.1261T>G (p.Ser421Ala) | |
13 | g.113149443T= | CA2120140768 | F10 | c.1393T= (p.Ser465=) c.*384T= (n.*384T=) c.1261T= (p.Ser421=) | |
13 | g.113149444C>A | CA388794528 | F10 | c.1394C>A (p.Ser465Tyr) c.*385C>A (n.*385C>A) c.1262C>A (p.Ser421Tyr) | |
13 | g.113149444C>G | CA388794529 | F10 | c.1394C>G (p.Ser465Cys) c.*385C>G (n.*385C>G) c.1262C>G (p.Ser421Cys) | |
13 | g.113149444C>T | CA388794531 | F10 | c.1394C>T (p.Ser465Phe) c.*385C>T (n.*385C>T) c.1262C>T (p.Ser421Phe) | |
13 | g.113149445C>A | CA485425181 | F10 | c.1395C>A (p.Ser465=) c.*386C>A (n.*386C>A) c.1263C>A (p.Ser421=) | |
13 | g.113149445C>G | CA485425185 | F10 | c.1395C>G (p.Ser465=) c.*386C>G (n.*386C>G) c.1263C>G (p.Ser421=) | |
13 | g.113149445C>T | CA485425184 | F10 | c.1395C>T (p.Ser465=) c.*386C>T (n.*386C>T) c.1263C>T (p.Ser421=) | COSMIC |
13 | g.113149446A= | CA2120140772 | F10 | c.1396A= (p.Met466=) c.*387A= (n.*387A=) c.1264A= (p.Met422=) | |
13 | g.113149446A>C | CA388794533 | F10 | c.1396A>C (p.Met466Leu) c.*387A>C (n.*387A>C) c.1264A>C (p.Met422Leu) | |
13 | g.113149446A>G | CA256478752 | F10 | c.1396A>G (p.Met466Val) c.*387A>G (n.*387A>G) c.1264A>G (p.Met422Val) | dbSNP gnomAD v4 |
13 | g.113149446A>T | CA388794536 | F10 | c.1396A>T (p.Met466Leu) c.*387A>T (n.*387A>T) c.1264A>T (p.Met422Leu) | |
13 | g.113149447T>A | CA388794537 | F10 | c.1397T>A (p.Met466Lys) c.*388T>A (n.*388T>A) c.1265T>A (p.Met422Lys) | |
13 | g.113149447T>C | CA7060739 | F10 | c.1397T>C (p.Met466Thr) c.*388T>C (n.*388T>C) c.1265T>C (p.Met422Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.113149447T>G | CA388794540 | F10 | c.1397T>G (p.Met466Arg) c.*388T>G (n.*388T>G) c.1265T>G (p.Met422Arg) | |
13 | g.113149447T= | CA2120140779 | F10 | c.1397T= (p.Met466=) c.*388T= (n.*388T=) c.1265T= (p.Met422=) | |
13 | g.113149448G>A | CA388794542 | F10 | c.1398G>A (p.Met466Ile) c.*389G>A (n.*389G>A) c.1266G>A (p.Met422Ile) | |
13 | g.113149448G>C | CA388794543 | F10 | c.1398G>C (p.Met466Ile) c.*389G>C (n.*389G>C) c.1266G>C (p.Met422Ile) | |
13 | g.113149448G= | CA2120140783 | F10 | c.1398G= (p.Met466=) c.*389G= (n.*389G=) c.1266G= (p.Met422=) | |
13 | g.113149448G>T | CA388794545 | F10 | c.1398G>T (p.Met466Ile) c.*389G>T (n.*389G>T) c.1266G>T (p.Met422Ile) | |
13 | g.113149449A>C | CA388794550 | F10 | c.1399A>C (p.Lys467Gln) c.*390A>C (n.*390A>C) c.1267A>C (p.Lys423Gln) | |
13 | g.113149449A>G | CA388794547 | F10 | c.1399A>G (p.Lys467Glu) c.*390A>G (n.*390A>G) c.1267A>G (p.Lys423Glu) | |
13 | g.113149449A>T | CA388794549 | F10 | c.1399A>T (p.Lys467Ter) c.*390A>T (n.*390A>T) c.1267A>T (p.Lys423Ter) | gnomAD v4 |
13 | g.113149452dup | CA612868399 | F10 | c.1402dup (p.Thr468AsnfsTer?) c.*393dup (n.*393dup) c.1270dup (p.Thr424AsnfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.113149450A>C | CA388794552 | F10 | c.1400A>C (p.Lys467Thr) c.*391A>C (n.*391A>C) c.1268A>C (p.Lys423Thr) | |
13 | g.113149450A>G | CA388794554 | F10 | c.1400A>G (p.Lys467Arg) c.*391A>G (n.*391A>G) c.1268A>G (p.Lys423Arg) | |
13 | g.113149450A>T | CA388794556 | F10 | c.1400A>T (p.Lys467Ile) c.*391A>T (n.*391A>T) c.1268A>T (p.Lys423Ile) | |
13 | g.113149451A>C | CA388794558 | F10 | c.1401A>C (p.Lys467Asn) c.*392A>C (n.*392A>C) c.1269A>C (p.Lys423Asn) | |
13 | g.113149451A>G | CA485425225 | F10 | c.1401A>G (p.Lys467=) c.*392A>G (n.*392A>G) c.1269A>G (p.Lys423=) | |
13 | g.113149451A>T | CA388794559 | F10 | c.1401A>T (p.Lys467Asn) c.*392A>T (n.*392A>T) c.1269A>T (p.Lys423Asn) | |
13 | g.113149452A= | CA2120140787 | F10 | c.1402A= (p.Thr468=) c.*393A= (n.*393A=) c.1270A= (p.Thr424=) | |
13 | g.113149452A>C | CA7060740 | F10 | c.1402A>C (p.Thr468Pro) c.*393A>C (n.*393A>C) c.1270A>C (p.Thr424Pro) | dbSNP ExAC gnomAD v2 |
13 | g.113149452A>G | CA388794562 | F10 | c.1402A>G (p.Thr468Ala) c.*393A>G (n.*393A>G) c.1270A>G (p.Thr424Ala) | |
13 | g.113149452A>T | CA388794563 | F10 | c.1402A>T (p.Thr468Ser) c.*393A>T (n.*393A>T) c.1270A>T (p.Thr424Ser) | |
13 | g.113149453C>A | CA388794566 | F10 | c.1403C>A (p.Thr468Asn) c.*394C>A (n.*394C>A) c.1271C>A (p.Thr424Asn) | |
13 | g.113149453C= | CA2120140804 | F10 | c.1403C= (p.Thr468=) c.*394C= (n.*394C=) c.1271C= (p.Thr424=) | |
13 | g.113149453C>G | CA388794567 | F10 | c.1403C>G (p.Thr468Ser) c.*394C>G (n.*394C>G) c.1271C>G (p.Thr424Ser) | dbSNP |
13 | g.113149453C>T | CA388794569 | F10 | c.1403C>T (p.Thr468Ile) c.*394C>T (n.*394C>T) c.1271C>T (p.Thr424Ile) | dbSNP gnomAD v4 |
13 | g.113149456_113149480del | CA2623810410 | F10 | c.1406_1430del (p.Arg469MetfsTer6) c.*397_*421del (n.*397_*421del) c.1274_1298del (p.Arg425MetfsTer6) | gnomAD v4 |
13 | g.113149454C>A | CA485425244 | F10 | c.1404C>A (p.Thr468=) c.*395C>A (n.*395C>A) c.1272C>A (p.Thr424=) | |
13 | g.113149454C= | CA2120140809 | F10 | c.1404C= (p.Thr468=) c.*395C= (n.*395C=) c.1272C= (p.Thr424=) | |
13 | g.113149454C>G | CA485425246 | F10 | c.1404C>G (p.Thr468=) c.*395C>G (n.*395C>G) c.1272C>G (p.Thr424=) | |
13 | g.113149454C>T | CA485425247 | F10 | c.1404C>T (p.Thr468=) c.*395C>T (n.*395C>T) c.1272C>T (p.Thr424=) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149455A>C | CA485425249 | F10 | c.1405A>C (p.Arg469=) c.*396A>C (n.*396A>C) c.1273A>C (p.Arg425=) | |
13 | g.113149455A>G | CA388794571 | F10 | c.1405A>G (p.Arg469Gly) c.*396A>G (n.*396A>G) c.1273A>G (p.Arg425Gly) | |
13 | g.113149455A>T | CA388794572 | F10 | c.1405A>T (p.Arg469Trp) c.*396A>T (n.*396A>T) c.1273A>T (p.Arg425Trp) | |
13 | g.113149456G>A | CA7060741 | F10 | c.1406G>A (p.Arg469Lys) c.*397G>A (n.*397G>A) c.1274G>A (p.Arg425Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149456G>C | CA388794577 | F10 | c.1406G>C (p.Arg469Thr) c.*397G>C (n.*397G>C) c.1274G>C (p.Arg425Thr) | |
13 | g.113149456G= | CA2120140816 | F10 | c.1406G= (p.Arg469=) c.*397G= (n.*397G=) c.1274G= (p.Arg425=) | |
13 | g.113149456G>T | CA388794575 | F10 | c.1406G>T (p.Arg469Met) c.*397G>T (n.*397G>T) c.1274G>T (p.Arg425Met) | |
13 | g.113149459del | CA2623810415 | F10 | c.1409del (p.Gly470AlafsTer13) c.*400del (n.*400del) c.1277del (p.Gly426AlafsTer13) | gnomAD v4 |
13 | g.113149457G>A | CA485425263 | F10 | c.1407G>A (p.Arg469=) c.*398G>A (n.*398G>A) c.1275G>A (p.Arg425=) | |
13 | g.113149457G>C | CA388794581 | F10 | c.1407G>C (p.Arg469Ser) c.*398G>C (n.*398G>C) c.1275G>C (p.Arg425Ser) | |
13 | g.113149457G>T | CA388794579 | F10 | c.1407G>T (p.Arg469Ser) c.*398G>T (n.*398G>T) c.1275G>T (p.Arg425Ser) | gnomAD v4 |
13 | g.113149458G>A | CA7060742 | F10 | c.1408G>A (p.Gly470Ser) c.*399G>A (n.*399G>A) c.1276G>A (p.Gly426Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149458G>C | CA7060743 | F10 | c.1408G>C (p.Gly470Arg) c.*399G>C (n.*399G>C) c.1276G>C (p.Gly426Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149458G= | CA2120140822 | F10 | c.1408G= (p.Gly470=) c.*399G= (n.*399G=) c.1276G= (p.Gly426=) | |
13 | g.113149458G>T | CA388794584 | F10 | c.1408G>T (p.Gly470Cys) c.*399G>T (n.*399G>T) c.1276G>T (p.Gly426Cys) | |
13 | g.113149459G>A | CA388794586 | F10 | c.1409G>A (p.Gly470Asp) c.*400G>A (n.*400G>A) c.1277G>A (p.Gly426Asp) | dbSNP |
13 | g.113149459G>C | CA388794588 | F10 | c.1409G>C (p.Gly470Ala) c.*400G>C (n.*400G>C) c.1277G>C (p.Gly426Ala) | |
13 | g.113149459G= | CA2120140832 | F10 | c.1409G= (p.Gly470=) c.*400G= (n.*400G=) c.1277G= (p.Gly426=) | |
13 | g.113149459G>T | CA388794590 | F10 | c.1409G>T (p.Gly470Val) c.*400G>T (n.*400G>T) c.1277G>T (p.Gly426Val) | dbSNP |
13 | g.113149460C>A | CA485425289 | F10 | c.1410C>A (p.Gly470=) c.*401C>A (n.*401C>A) c.1278C>A (p.Gly426=) | |
13 | g.113149460C= | CA2120140837 | F10 | c.1410C= (p.Gly470=) c.*401C= (n.*401C=) c.1278C= (p.Gly426=) | |
13 | g.113149460C>G | CA485425294 | F10 | c.1410C>G (p.Gly470=) c.*401C>G (n.*401C>G) c.1278C>G (p.Gly426=) | |
13 | g.113149460C>T | CA485425290 | F10 | c.1410C>T (p.Gly470=) c.*401C>T (n.*401C>T) c.1278C>T (p.Gly426=) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.113149461T>A | CA388794592 | F10 | c.1411T>A (p.Leu471Met) c.*402T>A (n.*402T>A) c.1279T>A (p.Leu427Met) | |
13 | g.113149461T>C | CA485425298 | F10 | c.1411T>C (p.Leu471=) c.*402T>C (n.*402T>C) c.1279T>C (p.Leu427=) | |
13 | g.113149461T>G | CA388794593 | F10 | c.1411T>G (p.Leu471Val) c.*402T>G (n.*402T>G) c.1279T>G (p.Leu427Val) | |
13 | g.113149462T>A | CA388794596 | F10 | c.1412T>A (p.Leu471Ter) c.*403T>A (n.*403T>A) c.1280T>A (p.Leu427Ter) | |
13 | g.113149462T>C | CA388794598 | F10 | c.1412T>C (p.Leu471Ser) c.*403T>C (n.*403T>C) c.1280T>C (p.Leu427Ser) | |
13 | g.113149462T>G | CA388794600 | F10 | c.1412T>G (p.Leu471Trp) c.*403T>G (n.*403T>G) c.1280T>G (p.Leu427Trp) | |
13 | g.113149463G>A | CA485425308 | F10 | c.1413G>A (p.Leu471=) c.*404G>A (n.*404G>A) c.1281G>A (p.Leu427=) | gnomAD v4 |
13 | g.113149463G>C | CA388794602 | F10 | c.1413G>C (p.Leu471Phe) c.*404G>C (n.*404G>C) c.1281G>C (p.Leu427Phe) | |
13 | g.113149463G>T | CA388794603 | F10 | c.1413G>T (p.Leu471Phe) c.*404G>T (n.*404G>T) c.1281G>T (p.Leu427Phe) | |
13 | g.113149464C>A | CA388794607 | F10 | c.1414C>A (p.Pro472Thr) c.*405C>A (n.*405C>A) c.1282C>A (p.Pro428Thr) | |
13 | g.113149464C>G | CA388794604 | F10 | c.1414C>G (p.Pro472Ala) c.*405C>G (n.*405C>G) c.1282C>G (p.Pro428Ala) | |
13 | g.113149464C>T | CA388794605 | F10 | c.1414C>T (p.Pro472Ser) c.*405C>T (n.*405C>T) c.1282C>T (p.Pro428Ser) | |
13 | g.113149465C>A | CA388794608 | F10 | c.1415C>A (p.Pro472His) c.*406C>A (n.*406C>A) c.1283C>A (p.Pro428His) | |
13 | g.113149465C= | CA2120140842 | F10 | c.1415C= (p.Pro472=) c.*406C= (n.*406C=) c.1283C= (p.Pro428=) | |
13 | g.113149465C>G | CA388794610 | F10 | c.1415C>G (p.Pro472Arg) c.*406C>G (n.*406C>G) c.1283C>G (p.Pro428Arg) | |
13 | g.113149465C>T | CA388794611 | F10 | c.1415C>T (p.Pro472Leu) c.*406C>T (n.*406C>T) c.1283C>T (p.Pro428Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149466C>A | CA485425331 | F10 | c.1416C>A (p.Pro472=) c.*407C>A (n.*407C>A) c.1284C>A (p.Pro428=) | |
13 | g.113149466C= | CA2120140852 | F10 | c.1416C= (p.Pro472=) c.*407C= (n.*407C=) c.1284C= (p.Pro428=) | |
13 | g.113149466C>G | CA485425334 | F10 | c.1416C>G (p.Pro472=) c.*407C>G (n.*407C>G) c.1284C>G (p.Pro428=) | |
13 | g.113149466C>T | CA256478756 | F10 | c.1416C>T (p.Pro472=) c.*407C>T (n.*407C>T) c.1284C>T (p.Pro428=) | dbSNP COSMIC |
13 | g.113149467A= | CA2120140857 | F10 | c.1417A= (p.Lys473=) c.*408A= (n.*408A=) c.1285A= (p.Lys429=) | |
13 | g.113149467A>C | CA388794613 | F10 | c.1417A>C (p.Lys473Gln) c.*408A>C (n.*408A>C) c.1285A>C (p.Lys429Gln) | |
13 | g.113149467A>G | CA388794615 | F10 | c.1417A>G (p.Lys473Glu) c.*408A>G (n.*408A>G) c.1285A>G (p.Lys429Glu) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149467A>T | CA388794616 | F10 | c.1417A>T (p.Lys473Ter) c.*408A>T (n.*408A>T) c.1285A>T (p.Lys429Ter) | |
13 | g.113149468A= | CA2120140865 | F10 | c.1418A= (p.Lys473=) c.*409A= (n.*409A=) c.1286A= (p.Lys429=) | |
13 | g.113149468A>C | CA388794617 | F10 | c.1418A>C (p.Lys473Thr) c.*409A>C (n.*409A>C) c.1286A>C (p.Lys429Thr) | |
13 | g.113149468A>G | CA256478758 | F10 | c.1418A>G (p.Lys473Arg) c.*409A>G (n.*409A>G) c.1286A>G (p.Lys429Arg) | dbSNP |
13 | g.113149468A>T | CA388794620 | F10 | c.1418A>T (p.Lys473Met) c.*409A>T (n.*409A>T) c.1286A>T (p.Lys429Met) | |
13 | g.113149469G>A | CA485425347 | F10 | c.1419G>A (p.Lys473=) c.*410G>A (n.*410G>A) c.1287G>A (p.Lys429=) | |
13 | g.113149469G>C | CA388794623 | F10 | c.1419G>C (p.Lys473Asn) c.*410G>C (n.*410G>C) c.1287G>C (p.Lys429Asn) | |
13 | g.113149469G>T | CA388794624 | F10 | c.1419G>T (p.Lys473Asn) c.*410G>T (n.*410G>T) c.1287G>T (p.Lys429Asn) | |
13 | g.113149470G>A | CA388794630 | F10 | c.1420G>A (p.Ala474Thr) c.*411G>A (n.*411G>A) c.1288G>A (p.Ala430Thr) | |
13 | g.113149470G>C | CA388794628 | F10 | c.1420G>C (p.Ala474Pro) c.*411G>C (n.*411G>C) c.1288G>C (p.Ala430Pro) | |
13 | g.113149470G>T | CA388794627 | F10 | c.1420G>T (p.Ala474Ser) c.*411G>T (n.*411G>T) c.1288G>T (p.Ala430Ser) |