Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.52676334C>A | CA6586173 | KRT1 | c.1416G>T (p.Lys472Asn) n.490G>T | dbSNP ExAC gnomAD v2 |
12 | g.52676334C= | CA2036619581 | KRT1 | c.1416G= (p.Lys472=) n.490G= | |
12 | g.52676334C>G | CA384962366 | KRT1 | c.1416G>C (p.Lys472Asn) n.490G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676334C>T | CA479872170 | KRT1 | c.1416G>A (p.Lys472=) n.490G>A | dbSNP gnomAD v2 gnomAD v4 |
12 | g.52676335T>A | CA384962369 | KRT1 | c.1415A>T (p.Lys472Met) n.489A>T | |
12 | g.52676335T>C | CA384962372 | KRT1 | c.1415A>G (p.Lys472Arg) n.489A>G | gnomAD v4 |
12 | g.52676335T>G | CA384962370 | KRT1 | c.1415A>C (p.Lys472Thr) n.489A>C | |
12 | g.52676336T>A | CA384962374 | KRT1 | c.1414A>T (p.Lys472Ter) n.488A>T | |
12 | g.52676336T>C | CA384962376 | KRT1 | c.1414A>G (p.Lys472Glu) n.488A>G | |
12 | g.52676336T>G | CA384962377 | KRT1 | c.1414A>C (p.Lys472Gln) n.488A>C | |
12 | g.52676337T>A | CA479873082 | KRT1 | c.1413A>T (p.Thr471=) n.487A>T | dbSNP |
12 | g.52676337T>C | CA479873084 | KRT1 | c.1413A>G (p.Thr471=) n.487A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676337T>G | CA6586174 | KRT1 | c.1413A>C (p.Thr471=) n.487A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676337T= | CA217417 | KRT1 | c.1413A= (p.Thr471=) n.487A= | |
12 | g.52676338G>A | CA384962383 | KRT1 | c.1412C>T (p.Thr471Ile) n.486C>T | |
12 | g.52676338G>C | CA384962385 | KRT1 | c.1412C>G (p.Thr471Arg) n.486C>G c.1412C>G (p.Thr471Ser) | |
12 | g.52676338G>T | CA384962386 | KRT1 | c.1412C>A (p.Thr471Lys) n.486C>A c.1412C>A (p.Thr471Asn) | |
12 | g.52676339T>A | CA384962389 | KRT1 | c.1411A>T (p.Thr471Ser) n.485A>T | |
12 | g.52676339T>C | CA384962391 | KRT1 | c.1411A>G (p.Thr471Ala) n.485A>G | |
12 | g.52676339T>G | CA384962393 | KRT1 | c.1411A>C (p.Thr471Pro) n.485A>C | |
12 | g.52676340G>A | CA479873111 | KRT1 | c.1410C>T (p.Asn470=) n.484C>T | dbSNP gnomAD v4 |
12 | g.52676340G>C | CA384962396 | KRT1 | c.1410C>G (p.Asn470Lys) n.484C>G | |
12 | g.52676340G= | CA2036619582 | KRT1 | c.1410C= (p.Asn470=) n.484C= | |
12 | g.52676340G>T | CA384962395 | KRT1 | c.1410C>A (p.Asn470Lys) n.484C>A | |
12 | g.52676341T>A | CA384962398 | KRT1 | c.1409A>T (p.Asn470Ile) n.483A>T | |
12 | g.52676341T>C | CA384962399 | KRT1 | c.1409A>G (p.Asn470Ser) n.483A>G | |
12 | g.52676341T>G | CA384962400 | KRT1 | c.1409A>C (p.Asn470Thr) n.483A>C | |
12 | g.52676342T>A | CA384962402 | KRT1 | c.1408A>T (p.Asn470Tyr) n.482A>T | |
12 | g.52676342T>C | CA6586175 | KRT1 | c.1408A>G (p.Asn470Asp) n.482A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676342T>G | CA384962405 | KRT1 | c.1408A>C (p.Asn470His) n.482A>C | COSMIC |
12 | g.52676342T= | CA2036619583 | KRT1 | c.1408A= (p.Asn470=) n.482A= | |
12 | g.52676343C>A | CA384962408 | KRT1 | c.1407G>T (p.Met469Ile) n.481G>T | |
12 | g.52676343C>G | CA384962409 | KRT1 | c.1407G>C (p.Met469Ile) n.481G>C | |
12 | g.52676343C>T | CA384962411 | KRT1 | c.1407G>A (p.Met469Ile) n.481G>A | |
12 | g.52676344A= | CA2036619584 | KRT1 | c.1406T= (p.Met469=) n.480T= | |
12 | g.52676344A>C | CA384962414 | KRT1 | c.1406T>G (p.Met469Arg) n.480T>G | gnomAD v4 |
12 | g.52676344A>G | CA6586176 | KRT1 | c.1406T>C (p.Met469Thr) n.480T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676344A>T | CA384962416 | KRT1 | c.1406T>A (p.Met469Lys) n.480T>A | gnomAD v4 |
12 | g.52676345T>A | CA384962422 | KRT1 | c.1405A>T (p.Met469Leu) n.479A>T | |
12 | g.52676345T>C | CA384962424 | KRT1 | c.1405A>G (p.Met469Val) n.479A>G | |
12 | g.52676345T>G | CA384962420 | KRT1 | c.1405A>C (p.Met469Leu) n.479A>C | |
12 | g.52676346C>A | CA479873156 | KRT1 | c.1404G>T (p.Leu468=) n.478G>T | |
12 | g.52676346C>G | CA479873152 | KRT1 | c.1404G>C (p.Leu468=) n.478G>C | |
12 | g.52676346C>T | CA479873148 | KRT1 | c.1404G>A (p.Leu468=) n.478G>A | |
12 | g.52676347A>C | CA384962434 | KRT1 | c.1403T>G (p.Leu468Arg) n.477T>G | |
12 | g.52676347A>G | CA384962429 | KRT1 | c.1403T>C (p.Leu468Pro) n.477T>C | gnomAD v4 |
12 | g.52676347A>T | CA384962431 | KRT1 | c.1403T>A (p.Leu468Gln) n.477T>A | |
12 | g.52676348G>A | CA479873160 | KRT1 | c.1402C>T (p.Leu468=) n.476C>T | dbSNP gnomAD v4 |
12 | g.52676348G>C | CA384962437 | KRT1 | c.1402C>G (p.Leu468Val) n.476C>G | |
12 | g.52676348G= | CA2036619585 | KRT1 | c.1402C= (p.Leu468=) n.476C= | |
12 | g.52676348G>T | CA384962440 | KRT1 | c.1402C>A (p.Leu468Met) n.476C>A | gnomAD v4 |
12 | g.52676349C>A | CA384962442 | KRT1 | c.1401G>T (p.Glu467Asp) n.475G>T | |
12 | g.52676349C>G | CA384962444 | KRT1 | c.1401G>C (p.Glu467Asp) n.475G>C | |
12 | g.52676349C>T | CA479873170 | KRT1 | c.1401G>A (p.Glu467=) n.475G>A | gnomAD v4 |
12 | g.52676350T>A | CA384962448 | KRT1 | c.1400A>T (p.Glu467Val) n.474A>T | |
12 | g.52676350T>C | CA384962450 | KRT1 | c.1400A>G (p.Glu467Gly) n.474A>G | |
12 | g.52676350T>G | CA384962453 | KRT1 | c.1400A>C (p.Glu467Ala) n.474A>C | |
12 | g.52676350_52676374delinsTCCTGGTAGTCGCGCAGCAGGCGGG | CA2036619586 | KRT1 | c.1376_1400delinsCCCGCCTGCTGCGCGACTACCAGGA (p.Ala459=) n.450_474delinsCCCGCCTGCTGCGCGACTACCAGGA | |
12 | g.52676351C>A | CA384962458 | KRT1 | c.1399G>T (p.Glu467Ter) n.473G>T | gnomAD v4 |
12 | g.52676351C= | CA2036619587 | KRT1 | c.1399G= (p.Glu467=) n.473G= | |
12 | g.52676351C>G | CA6586177 | KRT1 | c.1399G>C (p.Glu467Gln) n.473G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676351C>T | CA384962463 | KRT1 | c.1399G>A (p.Glu467Lys) n.473G>A | gnomAD v4 |
12 | g.52676353_52676376del | CA217413 | KRT1 | c.1376_1399del (p.Ala459_Gln466del) n.450_473del | ClinVar dbSNP |
12 | g.52676352C>A | CA384962466 | KRT1 | c.1398G>T (p.Gln466His) n.472G>T | |
12 | g.52676352C>G | CA384962469 | KRT1 | c.1398G>C (p.Gln466His) n.472G>C | |
12 | g.52676352C>T | CA479873192 | KRT1 | c.1398G>A (p.Gln466=) n.472G>A | |
12 | g.52676353T>A | CA384962470 | KRT1 | c.1397A>T (p.Gln466Leu) n.471A>T | |
12 | g.52676353T>C | CA6586178 | KRT1 | c.1397A>G (p.Gln466Arg) n.471A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676353T>G | CA384962471 | KRT1 | c.1397A>C (p.Gln466Pro) n.471A>C | |
12 | g.52676353T= | CA2036619588 | KRT1 | c.1397A= (p.Gln466=) n.471A= | |
12 | g.52676354G>A | CA384962472 | KRT1 | c.1396C>T (p.Gln466Ter) n.470C>T | |
12 | g.52676354G>C | CA384962474 | KRT1 | c.1396C>G (p.Gln466Glu) n.470C>G | |
12 | g.52676354G>T | CA384962476 | KRT1 | c.1396C>A (p.Gln466Lys) n.470C>A | |
12 | g.52676355G>A | CA479873219 | KRT1 | c.1395C>T (p.Tyr465=) n.469C>T | |
12 | g.52676355G>C | CA384962478 | KRT1 | c.1395C>G (p.Tyr465Ter) n.469C>G | |
12 | g.52676355G>T | CA384962481 | KRT1 | c.1395C>A (p.Tyr465Ter) n.469C>A | COSMIC |
12 | g.52676356T>A | CA384962484 | KRT1 | c.1394A>T (p.Tyr465Phe) n.468A>T | |
12 | g.52676356T>C | CA384962486 | KRT1 | c.1394A>G (p.Tyr465Cys) n.468A>G | dbSNP gnomAD v2 gnomAD v4 COSMIC |
12 | g.52676356T>G | CA384962489 | KRT1 | c.1394A>C (p.Tyr465Ser) n.468A>C | |
12 | g.52676356T= | CA2036619589 | KRT1 | c.1394A= (p.Tyr465=) n.468A= | |
12 | g.52676357A= | CA2036619590 | KRT1 | c.1393T= (p.Tyr465=) n.467T= | |
12 | g.52676357A>C | CA384962495 | KRT1 | c.1393T>G (p.Tyr465Asp) n.467T>G | dbSNP gnomAD v2 gnomAD v4 |
12 | g.52676357A>G | CA384962497 | KRT1 | c.1393T>C (p.Tyr465His) n.467T>C | |
12 | g.52676357A>T | CA384962493 | KRT1 | c.1393T>A (p.Tyr465Asn) n.467T>A | |
12 | g.52676358G>A | CA479873243 | KRT1 | c.1392C>T (p.Asp464=) n.466C>T | |
12 | g.52676358G>C | CA384962501 | KRT1 | c.1392C>G (p.Asp464Glu) n.466C>G | |
12 | g.52676358G>T | CA384962503 | KRT1 | c.1392C>A (p.Asp464Glu) n.466C>A | |
12 | g.52676359T>A | CA384962507 | KRT1 | c.1391A>T (p.Asp464Val) n.465A>T | |
12 | g.52676359T>C | CA384962510 | KRT1 | c.1391A>G (p.Asp464Gly) n.465A>G | |
12 | g.52676359T>G | CA384962513 | KRT1 | c.1391A>C (p.Asp464Ala) n.465A>C | |
12 | g.52676360C>A | CA384962516 | KRT1 | c.1390G>T (p.Asp464Tyr) n.464G>T | |
12 | g.52676360C= | CA2036619591 | KRT1 | c.1390G= (p.Asp464=) n.464G= | |
12 | g.52676360C>G | CA384962519 | KRT1 | c.1390G>C (p.Asp464His) n.464G>C | |
12 | g.52676360C>T | CA6586179 | KRT1 | c.1390G>A (p.Asp464Asn) n.464G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.52676361G>A | CA217415 | KRT1 | c.1389C>T (p.Arg463=) n.463C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676361G>C | CA237262386 | KRT1 | c.1389C>G (p.Arg463=) n.463C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676361G= | CA2036619592 | KRT1 | c.1389C= (p.Arg463=) n.463C= | |
12 | g.52676361G>T | CA479873274 | KRT1 | c.1389C>A (p.Arg463=) n.463C>A | gnomAD v4 |
12 | g.52676362C>A | CA384962525 | KRT1 | c.1388G>T (p.Arg463Leu) n.462G>T | |
12 | g.52676362C= | CA2036619593 | KRT1 | c.1388G= (p.Arg463=) n.462G= | |
12 | g.52676362C>G | CA384962528 | KRT1 | c.1388G>C (p.Arg463Pro) n.462G>C | |
12 | g.52676362C>T | CA6586180 | KRT1 | c.1388G>A (p.Arg463His) n.462G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676363G>A | CA6586181 | KRT1 | c.1387C>T (p.Arg463Cys) n.461C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.52676363G>C | CA384962536 | KRT1 | c.1387C>G (p.Arg463Gly) n.461C>G | gnomAD v3 gnomAD v4 |
12 | g.52676363G= | CA2036619594 | KRT1 | c.1387C= (p.Arg463=) n.461C= | |
12 | g.52676363G>T | CA384962532 | KRT1 | c.1387C>A (p.Arg463Ser) n.461C>A | gnomAD v4 |
12 | g.52676364C>A | CA479873296 | KRT1 | c.1386G>T (p.Leu462=) n.460G>T | |
12 | g.52676364C>G | CA479873299 | KRT1 | c.1386G>C (p.Leu462=) n.460G>C | |
12 | g.52676364C>T | CA479873301 | KRT1 | c.1386G>A (p.Leu462=) n.460G>A | |
12 | g.52676365A= | CA2036619595 | KRT1 | c.1385T= (p.Leu462=) n.459T= | |
12 | g.52676365A>C | CA384962540 | KRT1 | c.1385T>G (p.Leu462Arg) n.459T>G | |
12 | g.52676365A>G | CA384962542 | KRT1 | c.1385T>C (p.Leu462Pro) n.459T>C | |
12 | g.52676365A>T | CA384962545 | KRT1 | c.1385T>A (p.Leu462Gln) n.459T>A | dbSNP |
12 | g.52676366G>A | CA479873314 | KRT1 | c.1384C>T (p.Leu462=) n.458C>T | |
12 | g.52676366G>C | CA384962548 | KRT1 | c.1384C>G (p.Leu462Val) n.458C>G | |
12 | g.52676366G>T | CA384962551 | KRT1 | c.1384C>A (p.Leu462Met) n.458C>A | |
12 | g.52676367C>A | CA479873326 | KRT1 | c.1383G>T (p.Leu461=) n.457G>T | |
12 | g.52676367C>G | CA479873324 | KRT1 | c.1383G>C (p.Leu461=) n.457G>C | |
12 | g.52676367C>T | CA479873321 | KRT1 | c.1383G>A (p.Leu461=) n.457G>A | |
12 | g.52676368A>C | CA384962562 | KRT1 | c.1382T>G (p.Leu461Arg) n.456T>G | |
12 | g.52676368A>G | CA384962555 | KRT1 | c.1382T>C (p.Leu461Pro) n.456T>C | |
12 | g.52676368A>T | CA384962559 | KRT1 | c.1382T>A (p.Leu461Gln) n.456T>A | |
12 | g.52676369G>A | CA6586182 | KRT1 | c.1381C>T (p.Leu461=) n.455C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676369G>C | CA384962566 | KRT1 | c.1381C>G (p.Leu461Val) n.455C>G | |
12 | g.52676369G= | CA2036619596 | KRT1 | c.1381C= (p.Leu461=) n.455C= | |
12 | g.52676369G>T | CA384962569 | KRT1 | c.1381C>A (p.Leu461Met) n.455C>A | |
12 | g.52676370G>A | CA479873347 | KRT1 | c.1380C>T (p.Arg460=) n.454C>T | dbSNP |
12 | g.52676370G>C | CA479873350 | KRT1 | c.1380C>G (p.Arg460=) n.454C>G | |
12 | g.52676370G= | CA2036619597 | KRT1 | c.1380C= (p.Arg460=) n.454C= | |
12 | g.52676370G>T | CA479873353 | KRT1 | c.1380C>A (p.Arg460=) n.454C>A | |
12 | g.52676371C>A | CA6586183 | KRT1 | c.1379G>T (p.Arg460Leu) n.453G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676371C= | CA2036619598 | KRT1 | c.1379G= (p.Arg460=) n.453G= | |
12 | g.52676371C>G | CA384962570 | KRT1 | c.1379G>C (p.Arg460Pro) n.453G>C | |
12 | g.52676371C>T | CA237262424 | KRT1 | c.1379G>A (p.Arg460His) n.453G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676372G>A | CA6586184 | KRT1 | c.1378C>T (p.Arg460Cys) n.452C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676372G>C | CA6586185 | KRT1 | c.1378C>G (p.Arg460Gly) n.452C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676372G= | CA2036619599 | KRT1 | c.1378C= (p.Arg460=) n.452C= | |
12 | g.52676372G>T | CA384962573 | KRT1 | c.1378C>A (p.Arg460Ser) n.452C>A | COSMIC |
12 | g.52676373G>A | CA479873375 | KRT1 | c.1377C>T (p.Ala459=) n.451C>T | |
12 | g.52676373G>C | CA479873383 | KRT1 | c.1377C>G (p.Ala459=) n.451C>G | |
12 | g.52676373G>T | CA479873379 | KRT1 | c.1377C>A (p.Ala459=) n.451C>A | |
12 | g.52676374G>A | CA237262449 | KRT1 | c.1376C>T (p.Ala459Val) n.450C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676374G>C | CA6586186 | KRT1 | c.1376C>G (p.Ala459Gly) n.450C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676374G= | CA2036619600 | KRT1 | c.1376C= (p.Ala459=) n.450C= | |
12 | g.52676374G>T | CA384962586 | KRT1 | c.1376C>A (p.Ala459Asp) n.450C>A | |
12 | g.52676375C>A | CA384962592 | KRT1 | c.1375G>T (p.Ala459Ser) n.449G>T | |
12 | g.52676375C= | CA2036619601 | KRT1 | c.1375G= (p.Ala459=) n.449G= | |
12 | g.52676375C>G | CA384962594 | KRT1 | c.1375G>C (p.Ala459Pro) n.449G>C | dbSNP |
12 | g.52676375C>T | CA384962596 | KRT1 | c.1375G>A (p.Ala459Thr) n.449G>A | |
12 | g.52676376C>A | CA479873395 | KRT1 | c.1374G>T (p.Leu458=) n.448G>T | |
12 | g.52676376C>G | CA479873398 | KRT1 | c.1374G>C (p.Leu458=) n.448G>C | |
12 | g.52676376C>T | CA479873402 | KRT1 | c.1374G>A (p.Leu458=) n.448G>A | |
12 | g.52676377A>C | CA384962598 | KRT1 | c.1373T>G (p.Leu458Arg) n.447T>G | |
12 | g.52676377A>G | CA384962603 | KRT1 | c.1373T>C (p.Leu458Pro) n.447T>C | |
12 | g.52676377A>T | CA384962599 | KRT1 | c.1373T>A (p.Leu458Gln) n.447T>A | |
12 | g.52676378G>A | CA479873413 | KRT1 | c.1372C>T (p.Leu458=) n.446C>T | |
12 | g.52676378G>C | CA384962605 | KRT1 | c.1372C>G (p.Leu458Val) n.446C>G | |
12 | g.52676378G>T | CA384962606 | KRT1 | c.1372C>A (p.Leu458Met) n.446C>A | |
12 | g.52676379G>A | CA479873422 | KRT1 | c.1371C>T (p.Asp457=) n.445C>T | dbSNP gnomAD v4 |
12 | g.52676379G>C | CA384962610 | KRT1 | c.1371C>G (p.Asp457Glu) n.445C>G | |
12 | g.52676379G= | CA2036619602 | KRT1 | c.1371C= (p.Asp457=) n.445C= | |
12 | g.52676379G>T | CA384962612 | KRT1 | c.1371C>A (p.Asp457Glu) n.445C>A | |
12 | g.52676380T>A | CA384962619 | KRT1 | c.1370A>T (p.Asp457Val) n.444A>T | |
12 | g.52676380T>C | CA384962614 | KRT1 | c.1370A>G (p.Asp457Gly) n.444A>G | |
12 | g.52676380T>G | CA384962617 | KRT1 | c.1370A>C (p.Asp457Ala) n.444A>C | dbSNP |
12 | g.52676380T= | CA2036619603 | KRT1 | c.1370A= (p.Asp457=) n.444A= | |
12 | g.52676381C>A | CA6586187 | KRT1 | c.1369G>T (p.Asp457Tyr) n.443G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676381C= | CA2036619604 | KRT1 | c.1369G= (p.Asp457=) n.443G= | |
12 | g.52676381C>G | CA384962624 | KRT1 | c.1369G>C (p.Asp457His) n.443G>C | |
12 | g.52676381C>T | CA384962626 | KRT1 | c.1369G>A (p.Asp457Asn) n.443G>A | gnomAD v4 COSMIC |
12 | g.52676382T>A | CA384962629 | KRT1 | c.1368A>T (p.Glu456Asp) n.442A>T | dbSNP |
12 | g.52676382T>C | CA479873447 | KRT1 | c.1368A>G (p.Glu456=) n.442A>G | |
12 | g.52676382T>G | CA384962632 | KRT1 | c.1368A>C (p.Glu456Asp) n.442A>C | |
12 | g.52676382T= | CA2036619605 | KRT1 | c.1368A= (p.Glu456=) n.442A= | |
12 | g.52676383T>A | CA384962635 | KRT1 | c.1367A>T (p.Glu456Val) n.441A>T | |
12 | g.52676383T>C | CA384962637 | KRT1 | c.1367A>G (p.Glu456Gly) n.441A>G | dbSNP gnomAD v4 |
12 | g.52676383T>G | CA384962641 | KRT1 | c.1367A>C (p.Glu456Ala) n.441A>C | |
12 | g.52676383T= | CA2036619606 | KRT1 | c.1367A= (p.Glu456=) n.441A= | |
12 | g.52676384C>A | CA384962644 | KRT1 | c.1366G>T (p.Glu456Ter) n.440G>T | |
12 | g.52676384C>G | CA384962646 | KRT1 | c.1366G>C (p.Glu456Gln) n.440G>C | |
12 | g.52676384C>T | CA384962653 | KRT1 | c.1366G>A (p.Glu456Lys) n.440G>A | |
12 | g.52676385C>A | CA384962656 | KRT1 | c.1365G>T (p.Lys455Asn) n.439G>T | COSMIC |
12 | g.52676385C>G | CA384962659 | KRT1 | c.1365G>C (p.Lys455Asn) n.439G>C | |
12 | g.52676385C>T | CA479873472 | KRT1 | c.1365G>A (p.Lys455=) n.439G>A | gnomAD v4 COSMIC |
12 | g.52676386T>A | CA384962677 | KRT1 | c.1364A>T (p.Lys455Met) n.438A>T | |
12 | g.52676386T>C | CA384962662 | KRT1 | c.1364A>G (p.Lys455Arg) n.438A>G | dbSNP gnomAD v3 gnomAD v4 |
12 | g.52676386T>G | CA384962674 | KRT1 | c.1364A>C (p.Lys455Thr) n.438A>C | |
12 | g.52676386T= | CA2036619607 | KRT1 | c.1364A= (p.Lys455=) n.438A= | |
12 | g.52676387T>A | CA384962679 | KRT1 | c.1363A>T (p.Lys455Ter) n.437A>T | |
12 | g.52676387T>C | CA384962680 | KRT1 | c.1363A>G (p.Lys455Glu) n.437A>G | |
12 | g.52676387T>G | CA384962684 | KRT1 | c.1363A>C (p.Lys455Gln) n.437A>C | |
12 | g.52676388G>A | CA6586188 | KRT1 | c.1362C>T (p.Ala454=) n.436C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676388G>C | CA479873487 | KRT1 | c.1362C>G (p.Ala454=) n.436C>G | |
12 | g.52676388G= | CA2036619608 | KRT1 | c.1362C= (p.Ala454=) n.436C= | |
12 | g.52676388G>T | CA479873489 | KRT1 | c.1362C>A (p.Ala454=) n.436C>A | |
12 | g.52676389G>A | CA384962695 | KRT1 | c.1361C>T (p.Ala454Val) n.435C>T | dbSNP gnomAD v2 gnomAD v4 |
12 | g.52676389G>C | CA384962700 | KRT1 | c.1361C>G (p.Ala454Gly) n.435C>G | |
12 | g.52676389G= | CA2036619609 | KRT1 | c.1361C= (p.Ala454=) n.435C= | |
12 | g.52676389G>T | CA384962702 | KRT1 | c.1361C>A (p.Ala454Asp) n.435C>A | gnomAD v4 |
12 | g.52676390C>A | CA217411 | KRT1 | c.1360G>T (p.Ala454Ser) n.434G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676390C= | CA2036619610 | KRT1 | c.1360G= (p.Ala454=) n.434G= | |
12 | g.52676390C>G | CA384962705 | KRT1 | c.1360G>C (p.Ala454Pro) n.434G>C | dbSNP |
12 | g.52676390C>T | CA384962708 | KRT1 | c.1360G>A (p.Ala454Thr) n.434G>A | dbSNP gnomAD v2 |
12 | g.52676391C>A | CA384962715 | KRT1 | c.1359G>T (p.Gln453His) n.433G>T | |
12 | g.52676391C>G | CA384962718 | KRT1 | c.1359G>C (p.Gln453His) n.433G>C | |
12 | g.52676391C>T | CA479873510 | KRT1 | c.1359G>A (p.Gln453=) n.433G>A | gnomAD v4 |
12 | g.52676392T>A | CA384962722 | KRT1 | c.1358A>T (p.Gln453Leu) n.432A>T | dbSNP |
12 | g.52676392T>C | CA384962731 | KRT1 | c.1358A>G (p.Gln453Arg) n.432A>G | |
12 | g.52676392T>G | CA384962733 | KRT1 | c.1358A>C (p.Gln453Pro) n.432A>C | ClinVar dbSNP |
12 | g.52676392T= | CA2036619611 | KRT1 | c.1358A= (p.Gln453=) n.432A= | |
12 | g.52676393G>A | CA384962735 | KRT1 | c.1357C>T (p.Gln453Ter) n.431C>T | |
12 | g.52676393G>C | CA384962749 | KRT1 | c.1357C>G (p.Gln453Glu) n.431C>G | |
12 | g.52676393G>T | CA384962737 | KRT1 | c.1357C>A (p.Gln453Lys) n.431C>A | |
12 | g.52676394C>A | CA384962762 | KRT1 | c.1356G>T (p.Gln452His) n.430G>T | |
12 | g.52676394C>G | CA384962766 | KRT1 | c.1356G>C (p.Gln452His) n.430G>C | |
12 | g.52676394C>T | CA479873530 | KRT1 | c.1356G>A (p.Gln452=) n.430G>A | |
12 | g.52676395T>A | CA384962771 | KRT1 | c.1355A>T (p.Gln452Leu) n.429A>T | gnomAD v4 |
12 | g.52676395T>C | CA384962775 | KRT1 | c.1355A>G (p.Gln452Arg) n.429A>G | |
12 | g.52676395T>G | CA384962780 | KRT1 | c.1355A>C (p.Gln452Pro) n.429A>C | |
12 | g.52676396G>A | CA384962787 | KRT1 | c.1354C>T (p.Gln452Ter) n.428C>T | |
12 | g.52676396G>C | CA384962789 | KRT1 | c.1354C>G (p.Gln452Glu) n.428C>G | |
12 | g.52676396G>T | CA384962795 | KRT1 | c.1354C>A (p.Gln452Lys) n.428C>A | gnomAD v4 |
12 | g.52676397C>A | CA479873547 | KRT1 | c.1353G>T (p.Leu451=) n.427G>T | |
12 | g.52676397C>G | CA479873549 | KRT1 | c.1353G>C (p.Leu451=) n.427G>C | |
12 | g.52676397C>T | CA479873553 | KRT1 | c.1353G>A (p.Leu451=) n.427G>A | |
12 | g.52676398A= | CA2036619612 | KRT1 | c.1352T= (p.Leu451=) n.426T= | |
12 | g.52676398A>C | CA384962798 | KRT1 | c.1352T>G (p.Leu451Arg) n.426T>G | |
12 | g.52676398A>G | CA384962799 | KRT1 | c.1352T>C (p.Leu451Pro) n.426T>C | dbSNP gnomAD v4 |
12 | g.52676398A>T | CA384962802 | KRT1 | c.1352T>A (p.Leu451Gln) n.426T>A | |
12 | g.52676399G>A | CA6586189 | KRT1 | c.1351C>T (p.Leu451=) n.425C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676399G>C | CA384962827 | KRT1 | c.1351C>G (p.Leu451Val) n.425C>G | dbSNP gnomAD v4 |
12 | g.52676399G= | CA2036619613 | KRT1 | c.1351C= (p.Leu451=) n.425C= | |
12 | g.52676399G>T | CA384962822 | KRT1 | c.1351C>A (p.Leu451Met) n.425C>A | |
12 | g.52676400G>A | CA6586190 | KRT1 | c.1350C>T (p.Ala450=) n.424C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676400G>C | CA479873572 | KRT1 | c.1350C>G (p.Ala450=) n.424C>G | |
12 | g.52676400G= | CA2036619614 | KRT1 | c.1350C= (p.Ala450=) n.424C= | |
12 | g.52676400G>T | CA479873574 | KRT1 | c.1350C>A (p.Ala450=) n.424C>A | |
12 | g.52676401G>A | CA384962841 | KRT1 | c.1349C>T (p.Ala450Val) n.423C>T | |
12 | g.52676401G>C | CA6586191 | KRT1 | c.1349C>G (p.Ala450Gly) n.423C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676401G= | CA2036619615 | KRT1 | c.1349C= (p.Ala450=) n.423C= | |
12 | g.52676401G>T | CA384962844 | KRT1 | c.1349C>A (p.Ala450Asp) n.423C>A | ClinVar dbSNP |
12 | g.52676402C>A | CA384962847 | KRT1 | c.1348G>T (p.Ala450Ser) n.422G>T | |
12 | g.52676402C>G | CA384962848 | KRT1 | c.1348G>C (p.Ala450Pro) n.422G>C | |
12 | g.52676402C>T | CA384962849 | KRT1 | c.1348G>A (p.Ala450Thr) n.422G>A | gnomAD v4 |
12 | g.52676403A>C | CA384962850 | KRT1 | c.1347T>G (p.Asp449Glu) n.421T>G | |
12 | g.52676403A>G | CA479873594 | KRT1 | c.1347T>C (p.Asp449=) n.421T>C | |
12 | g.52676403A>T | CA384962853 | KRT1 | c.1347T>A (p.Asp449Glu) n.421T>A | |
12 | g.52676404T>A | CA6586192 | KRT1 | c.1346A>T (p.Asp449Val) n.420A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676404T>C | CA384962862 | KRT1 | c.1346A>G (p.Asp449Gly) n.420A>G | |
12 | g.52676404T>G | CA384962865 | KRT1 | c.1346A>C (p.Asp449Ala) n.420A>C | |
12 | g.52676404T= | CA2036619616 | KRT1 | c.1346A= (p.Asp449=) n.420A= | |
12 | g.52676405C>A | CA384962880 | KRT1 | c.1345G>T (p.Asp449Tyr) n.419G>T | |
12 | g.52676405C>G | CA384962890 | KRT1 | c.1345G>C (p.Asp449His) n.419G>C | |
12 | g.52676405C>T | CA384962892 | KRT1 | c.1345G>A (p.Asp449Asn) n.419G>A | |
12 | g.52676406C>A | CA384962894 | KRT1 | c.1344G>T (p.Glu448Asp) n.418G>T | |
12 | g.52676406C= | CA2036619617 | KRT1 | c.1344G= (p.Glu448=) n.418G= | |
12 | g.52676406C>G | CA384962896 | KRT1 | c.1344G>C (p.Glu448Asp) n.418G>C | |
12 | g.52676406C>T | CA479873614 | KRT1 | c.1344G>A (p.Glu448=) n.418G>A | dbSNP gnomAD v3 gnomAD v4 |
12 | g.52676407T>A | CA384962902 | KRT1 | c.1343A>T (p.Glu448Val) n.417A>T | |
12 | g.52676407T>C | CA384962907 | KRT1 | c.1343A>G (p.Glu448Gly) n.417A>G | |
12 | g.52676407T>G | CA384962910 | KRT1 | c.1343A>C (p.Glu448Ala) n.417A>C | |
12 | g.52676408C>A | CA384962913 | KRT1 | c.1342G>T (p.Glu448Ter) n.416G>T | |
12 | g.52676408C= | CA2036619618 | KRT1 | c.1342G= (p.Glu448=) n.416G= | |
12 | g.52676408C>G | CA384962915 | KRT1 | c.1342G>C (p.Glu448Gln) n.416G>C | dbSNP gnomAD v4 |
12 | g.52676408C>T | CA384962917 | KRT1 | c.1342G>A (p.Glu448Lys) n.416G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676409C>A | CA479873631 | KRT1 | c.1341G>T (p.Leu447=) n.415G>T | |
12 | g.52676409C>G | CA479873628 | KRT1 | c.1341G>C (p.Leu447=) n.415G>C | |
12 | g.52676409C>T | CA479873626 | KRT1 | c.1341G>A (p.Leu447=) n.415G>A | gnomAD v4 |
12 | g.52676410A= | CA2036619619 | KRT1 | c.1340T= (p.Leu447=) n.414T= | |
12 | g.52676410A>C | CA384962921 | KRT1 | c.1340T>G (p.Leu447Arg) n.414T>G | |
12 | g.52676410A>G | CA384962926 | KRT1 | c.1340T>C (p.Leu447Pro) n.414T>C | dbSNP |
12 | g.52676410A>T | CA384962928 | KRT1 | c.1340T>A (p.Leu447Gln) n.414T>A | |
12 | g.52676411G>A | CA479873636 | KRT1 | c.1339C>T (p.Leu447=) n.413C>T | |
12 | g.52676411G>C | CA384962929 | KRT1 | c.1339C>G (p.Leu447Val) n.413C>G | |
12 | g.52676411G>T | CA384962930 | KRT1 | c.1339C>A (p.Leu447Met) n.413C>A | |
12 | g.52676412G>A | CA479873639 | KRT1 | c.1338C>T (p.Asp446=) n.412C>T | gnomAD v4 |
12 | g.52676412G>C | CA384962931 | KRT1 | c.1338C>G (p.Asp446Glu) n.412C>G | |
12 | g.52676412G>T | CA384962934 | KRT1 | c.1338C>A (p.Asp446Glu) n.412C>A | dbSNP |
12 | g.52676413T>A | CA384962937 | KRT1 | c.1337A>T (p.Asp446Val) n.411A>T | dbSNP |
12 | g.52676413T>C | CA384962944 | KRT1 | c.1337A>G (p.Asp446Gly) n.411A>G | |
12 | g.52676413T>G | CA384962942 | KRT1 | c.1337A>C (p.Asp446Ala) n.411A>C | dbSNP |
12 | g.52676413T= | CA2036619620 | KRT1 | c.1337A= (p.Asp446=) n.411A= | |
12 | g.52676414C>A | CA384962950 | KRT1 | c.1336G>T (p.Asp446Tyr) n.410G>T | |
12 | g.52676414C>G | CA384962957 | KRT1 | c.1336G>C (p.Asp446His) n.410G>C | dbSNP |
12 | g.52676414C>T | CA384962960 | KRT1 | c.1336G>A (p.Asp446Asn) n.410G>A | |
12 | g.52676415A>C | CA384962961 | KRT1 | c.1335T>G (p.Asn445Lys) n.409T>G | |
12 | g.52676415A>G | CA479873660 | KRT1 | c.1335T>C (p.Asn445=) n.409T>C | gnomAD v4 |
12 | g.52676415A>T | CA384962963 | KRT1 | c.1335T>A (p.Asn445Lys) n.409T>A | |
12 | g.52676416T>A | CA384962970 | KRT1 | c.1334A>T (p.Asn445Ile) n.408A>T | |
12 | g.52676416T>C | CA384962975 | KRT1 | c.1334A>G (p.Asn445Ser) n.408A>G | |
12 | g.52676416T>G | CA384962979 | KRT1 | c.1334A>C (p.Asn445Thr) n.408A>C | |
12 | g.52676417T>A | CA384962982 | KRT1 | c.1333A>T (p.Asn445Tyr) n.407A>T | |
12 | g.52676417T>C | CA384962987 | KRT1 | c.1333A>G (p.Asn445Asp) n.407A>G | |
12 | g.52676417T>G | CA384962992 | KRT1 | c.1333A>C (p.Asn445His) n.407A>C | |
12 | g.52676418C>A | CA479873672 | KRT1 | c.1332G>T (p.Leu444=) n.406G>T | |
12 | g.52676418C>G | CA479873674 | KRT1 | c.1332G>C (p.Leu444=) n.406G>C | |
12 | g.52676418C>T | CA479873675 | KRT1 | c.1332G>A (p.Leu444=) n.406G>A | dbSNP COSMIC |
12 | g.52676419A>C | CA384963014 | KRT1 | c.1331T>G (p.Leu444Arg) n.405T>G | |
12 | g.52676419A>G | CA384963009 | KRT1 | c.1331T>C (p.Leu444Pro) n.405T>C | |
12 | g.52676419A>T | CA384962998 | KRT1 | c.1331T>A (p.Leu444Gln) n.405T>A | |
12 | g.52676420G>A | CA479873682 | KRT1 | c.1330C>T (p.Leu444=) n.404C>T | gnomAD v4 |
12 | g.52676420G>C | CA384963020 | KRT1 | c.1330C>G (p.Leu444Val) n.404C>G | |
12 | g.52676420G>T | CA384963032 | KRT1 | c.1330C>A (p.Leu444Met) n.404C>A | gnomAD v4 |
12 | g.52676421C>A | CA384963040 | KRT1 | c.1329G>T (p.Lys443Asn) n.403G>T | |
12 | g.52676421C>G | CA384963052 | KRT1 | c.1329G>C (p.Lys443Asn) n.403G>C | |
12 | g.52676421C>T | CA479873689 | KRT1 | c.1329G>A (p.Lys443=) n.403G>A | gnomAD v4 |
12 | g.52676422T>A | CA6586193 | KRT1 | c.1328A>T (p.Lys443Met) n.402A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676422T>C | CA384963057 | KRT1 | c.1328A>G (p.Lys443Arg) n.402A>G | |
12 | g.52676422T>G | CA384963058 | KRT1 | c.1328A>C (p.Lys443Thr) n.402A>C | |
12 | g.52676422T= | CA2036619621 | KRT1 | c.1328A= (p.Lys443=) n.402A= | |
12 | g.52676423T>A | CA384963061 | KRT1 | c.1327A>T (p.Lys443Ter) n.401A>T | |
12 | g.52676423T>C | CA384963074 | KRT1 | c.1327A>G (p.Lys443Glu) n.401A>G | |
12 | g.52676423T>G | CA384963076 | KRT1 | c.1327A>C (p.Lys443Gln) n.401A>C | |
12 | g.52676424G>A | CA479873697 | KRT1 | c.1326C>T (p.Asn442=) n.400C>T | gnomAD v4 |
12 | g.52676424G>C | CA384963078 | KRT1 | c.1326C>G (p.Asn442Lys) n.400C>G | dbSNP gnomAD v2 |
12 | g.52676424G= | CA2036619622 | KRT1 | c.1326C= (p.Asn442=) n.400C= | |
12 | g.52676424G>T | CA384963079 | KRT1 | c.1326C>A (p.Asn442Lys) n.400C>A | |
12 | g.52676425T>A | CA384963093 | KRT1 | c.1325A>T (p.Asn442Ile) n.399A>T | |
12 | g.52676425T>C | CA384963087 | KRT1 | c.1325A>G (p.Asn442Ser) n.399A>G | |
12 | g.52676425T>G | CA384963081 | KRT1 | c.1325A>C (p.Asn442Thr) n.399A>C | |
12 | g.52676426T>A | CA384963106 | KRT1 | c.1324A>T (p.Asn442Tyr) n.398A>T | gnomAD v4 |
12 | g.52676426T>C | CA384963119 | KRT1 | c.1324A>G (p.Asn442Asp) n.398A>G | |
12 | g.52676426T>G | CA384963113 | KRT1 | c.1324A>C (p.Asn442His) n.398A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676426T= | CA2036619623 | KRT1 | c.1324A= (p.Asn442=) n.398A= | |
12 | g.52676427C>A | CA384963127 | KRT1 | c.1323G>T (p.Lys441Asn) n.397G>T | COSMIC |
12 | g.52676427C= | CA2036619624 | KRT1 | c.1323G= (p.Lys441=) n.397G= | |
12 | g.52676427C>G | CA384963142 | KRT1 | c.1323G>C (p.Lys441Asn) n.397G>C | |
12 | g.52676427C>T | CA237262540 | KRT1 | c.1323G>A (p.Lys441=) n.397G>A | dbSNP gnomAD v4 |
12 | g.52676428T>A | CA384963155 | KRT1 | c.1322A>T (p.Lys441Met) n.396A>T | |
12 | g.52676428T>C | CA384963164 | KRT1 | c.1322A>G (p.Lys441Arg) n.396A>G | |
12 | g.52676428T>G | CA384963167 | KRT1 | c.1322A>C (p.Lys441Thr) n.396A>C | |
12 | g.52676429T>A | CA384963170 | KRT1 | c.1321A>T (p.Lys441Ter) n.395A>T | |
12 | g.52676429T>C | CA384963176 | KRT1 | c.1321A>G (p.Lys441Glu) n.395A>G | |
12 | g.52676429T>G | CA384963178 | KRT1 | c.1321A>C (p.Lys441Gln) n.395A>C | |
12 | g.52676430G>A | CA479873731 | KRT1 | c.1320C>T (p.Ala440=) n.394C>T | |
12 | g.52676430G>C | CA479873732 | KRT1 | c.1320C>G (p.Ala440=) n.394C>G | |
12 | g.52676430G>T | CA479873734 | KRT1 | c.1320C>A (p.Ala440=) n.394C>A | |
12 | g.52676435_52676446dup | CA2573148760 | KRT1 | c.1309_1320dup (p.Ala440_Lys441insLeuLysAspAla) n.383_394dup | ClinVar dbSNP |
12 | g.52676431G>A | CA384963212 | KRT1 | c.1319C>T (p.Ala440Val) n.393C>T | |
12 | g.52676431G>C | CA384963189 | KRT1 | c.1319C>G (p.Ala440Gly) n.393C>G | |
12 | g.52676431G>T | CA384963207 | KRT1 | c.1319C>A (p.Ala440Asp) n.393C>A | |
12 | g.52676431_52676432delinsAT | CA2695216818 | KRT1 | c.1318_1319delinsAT (p.Ala440Ile) n.392_393delinsAT | |
12 | g.52676432C>A | CA6586194 | KRT1 | c.1318G>T (p.Ala440Ser) n.392G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52676432C= | CA2036619625 | KRT1 | c.1318G= (p.Ala440=) n.392G= | |
12 | g.52676432C>G | CA384963222 | KRT1 | c.1318G>C (p.Ala440Pro) n.392G>C | |
12 | g.52676432C>T | CA384963228 | KRT1 | c.1318G>A (p.Ala440Thr) n.392G>A | ClinVar |
12 | g.52676433A>C | CA384963233 | KRT1 | c.1317T>G (p.Asp439Glu) n.391T>G | |
12 | g.52676433A>G | CA479873747 | KRT1 | c.1317T>C (p.Asp439=) n.391T>C | |
12 | g.52676433A>T | CA384963250 | KRT1 | c.1317T>A (p.Asp439Glu) n.391T>A | |
12 | g.52676434T>A | CA384963265 | KRT1 | c.1316A>T (p.Asp439Val) n.390A>T | |
12 | g.52676434T>C | CA6586195 | KRT1 | c.1316A>G (p.Asp439Gly) n.390A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52676434T>G | CA384963254 | KRT1 | c.1316A>C (p.Asp439Ala) n.390A>C | |
12 | g.52676434T= | CA2036619626 | KRT1 | c.1316A= (p.Asp439=) n.390A= |