Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583457_41583551del | CA2809495801 | KRT14 | c.1053+1_1054-1del n.503+1_504-1del | |
17 | g.41583525A= | CA2260085444 | KRT14 | c.1053+26T= (n.1053+26T=) n.503+26T= | |
17 | g.41583525A>C | CA8562526 | KRT14 | c.1053+26T>G (n.1053+26T>G) n.503+26T>G | dbSNP ExAC gnomAD v2 |
17 | g.41583525A>G | CA8562525 | KRT14 | c.1053+26T>C (n.1053+26T>C) n.503+26T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583526C= | CA2260085445 | KRT14 | c.1053+25G= (n.1053+25G=) n.503+25G= | |
17 | g.41583526C>G | CA8562527 | KRT14 | c.1053+25G>C (n.1053+25G>C) n.503+25G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583526C>T | CA2637834663 | KRT14 | c.1053+25G>A (n.1053+25G>A) n.503+25G>A | gnomAD v4 |
17 | g.41583528del | CA2566088433 | KRT14 | c.1053+23del (n.1053+23del) n.503+23del | |
17 | g.41583530C>A | CA2733826298 | KRT14 | c.1053+21G>T (n.1053+21G>T) n.503+21G>T | dbSNP |
17 | g.41583531C>G | CA2511190744 | KRT14 | c.1053+20G>C (n.1053+20G>C) n.503+20G>C | |
17 | g.41583532T>G | CA2536235823 | KRT14 | c.1053+19A>C (n.1053+19A>C) n.503+19A>C | |
17 | g.41583533T>C | CA8562528 | KRT14 | c.1053+18A>G (n.1053+18A>G) n.503+18A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583533T>G | CA2568545981 | KRT14 | c.1053+18A>C (n.1053+18A>C) n.503+18A>C | gnomAD v4 |
17 | g.41583533T= | CA2260085446 | KRT14 | c.1053+18A= (n.1053+18A=) n.503+18A= | |
17 | g.41583535del | CA2637834672 | KRT14 | c.1053+17del (n.1053+17del) n.503+17del | gnomAD v4 |
17 | g.41583536T>C | CA2514579406 | KRT14 | c.1053+15A>G (n.1053+15A>G) n.503+15A>G | |
17 | g.41583537G>T | CA2637834673 | KRT14 | c.1053+14C>A (n.1053+14C>A) n.503+14C>A | gnomAD v4 |
17 | g.41583538G>A | CA8562529 | KRT14 | c.1053+13C>T (n.1053+13C>T) n.503+13C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583538G= | CA2260085447 | KRT14 | c.1053+13C= (n.1053+13C=) n.503+13C= | |
17 | g.41583540_41583541insGCGCC | CA2512086332 | KRT14 | c.1053+10_1053+11insGGCGC (n.1053+10_1053+11insGGCGC) n.503+10_503+11insGGCGC | |
17 | g.41583541C= | CA2260085448 | KRT14 | c.1053+10G= (n.1053+10G=) n.503+10G= | |
17 | g.41583541C>G | CA626215426 | KRT14 | c.1053+10G>C (n.1053+10G>C) n.503+10G>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583542T>A | CA8562530 | KRT14 | c.1053+9A>T (n.1053+9A>T) n.503+9A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583542T>C | CA2576267610 | KRT14 | c.1053+9A>G (n.1053+9A>G) n.503+9A>G | gnomAD v4 |
17 | g.41583542T>G | CA2637834686 | KRT14 | c.1053+9A>C (n.1053+9A>C) n.503+9A>C | gnomAD v4 |
17 | g.41583542T= | CA2260085449 | KRT14 | c.1053+9A= (n.1053+9A=) n.503+9A= | |
17 | g.41583542_41583545del | CA2522214840 | KRT14 | c.1053+6_1053+9del (n.1053+6_1053+9del) n.503+6_503+9del | |
17 | g.41583543A= | CA2260085450 | KRT14 | c.1053+8T= (n.1053+8T=) n.503+8T= | |
17 | g.41583543A>G | CA626215427 | KRT14 | c.1053+8T>C (n.1053+8T>C) n.503+8T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583544T>C | CA772038527 | KRT14 | c.1053+7A>G (n.1053+7A>G) n.503+7A>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583544T= | CA2260085451 | KRT14 | c.1053+7A= (n.1053+7A=) n.503+7A= | |
17 | g.41583545T>G | CA2843324278 | KRT14 | c.1053+6A>C (n.1053+6A>C) n.503+6A>C | |
17 | g.41583546C= | CA2260085452 | KRT14 | c.1053+5G= (n.1053+5G=) n.503+5G= | |
17 | g.41583546C>T | CA2260085453 | KRT14 | c.1053+5G>A (n.1053+5G>A) n.503+5G>A | dbSNP gnomAD v4 |
17 | g.41583549A>C | CA399476236 | KRT14 | c.1053+2T>G (n.1053+2T>G) n.503+2T>G | |
17 | g.41583549A>G | CA399476238 | KRT14 | c.1053+2T>C (n.1053+2T>C) n.503+2T>C | gnomAD v4 |
17 | g.41583549A>T | CA399476239 | KRT14 | c.1053+2T>A (n.1053+2T>A) n.503+2T>A | |
17 | g.41583550C>A | CA399476243 | KRT14 | c.1053+1G>T (n.1053+1G>T) n.503+1G>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583550C= | CA2260085454 | KRT14 | c.1053+1G= (n.1053+1G=) n.503+1G= | |
17 | g.41583550C>G | CA399476245 | KRT14 | c.1053+1G>C (n.1053+1G>C) n.503+1G>C | |
17 | g.41583550C>T | CA399476248 | KRT14 | c.1053+1G>A (n.1053+1G>A) n.503+1G>A | ClinVar gnomAD v4 |
17 | g.41583551C>A | CA399476251 | KRT14 | c.1053G>T (p.Met351Ile) n.503G>T | |
17 | g.41583551C>G | CA399476256 | KRT14 | c.1053G>C (p.Met351Ile) n.503G>C | |
17 | g.41583551C>T | CA399476254 | KRT14 | c.1053G>A (p.Met351Ile) n.503G>A | COSMIC |
17 | g.41583552A>C | CA399476260 | KRT14 | c.1052T>G (p.Met351Arg) n.502T>G | |
17 | g.41583552A>G | CA399476266 | KRT14 | c.1052T>C (p.Met351Thr) n.502T>C | gnomAD v4 |
17 | g.41583552A>T | CA399476263 | KRT14 | c.1052T>A (p.Met351Lys) n.502T>A | |
17 | g.41583553T>A | CA399476268 | KRT14 | c.1051A>T (p.Met351Leu) n.501A>T | |
17 | g.41583553T>C | CA8562531 | KRT14 | c.1051A>G (p.Met351Val) n.501A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583553T>G | CA399476272 | KRT14 | c.1051A>C (p.Met351Leu) n.501A>C | |
17 | g.41583553T= | CA2260085455 | KRT14 | c.1051A= (p.Met351=) n.501A= | |
17 | g.41583554G>A | CA500205355 | KRT14 | c.1050C>T (p.Ser350=) n.500C>T | |
17 | g.41583554G>C | CA399476275 | KRT14 | c.1050C>G (p.Ser350Arg) n.500C>G | |
17 | g.41583554G>T | CA399476278 | KRT14 | c.1050C>A (p.Ser350Arg) n.500C>A | |
17 | g.41583555C>A | CA399476282 | KRT14 | c.1049G>T (p.Ser350Ile) n.499G>T | |
17 | g.41583555C= | CA2260085456 | KRT14 | c.1049G= (p.Ser350=) n.499G= | |
17 | g.41583555C>G | CA399476283 | KRT14 | c.1049G>C (p.Ser350Thr) n.499G>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583555C>T | CA399476286 | KRT14 | c.1049G>A (p.Ser350Asn) n.499G>A | |
17 | g.41583556T>A | CA399476289 | KRT14 | c.1048A>T (p.Ser350Cys) n.498A>T | |
17 | g.41583556T>C | CA399476292 | KRT14 | c.1048A>G (p.Ser350Gly) n.498A>G | |
17 | g.41583556T>G | CA399476294 | KRT14 | c.1048A>C (p.Ser350Arg) n.498A>C | |
17 | g.41583557G>A | CA500205358 | KRT14 | c.1047C>T (p.Leu349=) n.497C>T | |
17 | g.41583557G>C | CA500205356 | KRT14 | c.1047C>G (p.Leu349=) n.497C>G | |
17 | g.41583557G>T | CA500205357 | KRT14 | c.1047C>A (p.Leu349=) n.497C>A | |
17 | g.41583558A>C | CA399476301 | KRT14 | c.1046T>G (p.Leu349Arg) n.496T>G | |
17 | g.41583558A>G | CA399476299 | KRT14 | c.1046T>C (p.Leu349Pro) n.496T>C | |
17 | g.41583558A>T | CA399476297 | KRT14 | c.1046T>A (p.Leu349His) n.496T>A | |
17 | g.41583559G>A | CA399476304 | KRT14 | c.1045C>T (p.Leu349Phe) n.495C>T | gnomAD v4 |
17 | g.41583559G>C | CA399476306 | KRT14 | c.1045C>G (p.Leu349Val) n.495C>G | |
17 | g.41583559G= | CA2260085457 | KRT14 | c.1045C= (p.Leu349=) n.495C= | |
17 | g.41583559G>T | CA399476308 | KRT14 | c.1045C>A (p.Leu349Ile) n.495C>A | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583560C>A | CA399476311 | KRT14 | c.1044G>T (p.Gln348His) n.494G>T | |
17 | g.41583560C>G | CA399476313 | KRT14 | c.1044G>C (p.Gln348His) n.494G>C | |
17 | g.41583560C>T | CA500205359 | KRT14 | c.1044G>A (p.Gln348=) n.494G>A | COSMIC |
17 | g.41583561T>A | CA399476317 | KRT14 | c.1043A>T (p.Gln348Leu) n.493A>T | |
17 | g.41583561T>C | CA399476320 | KRT14 | c.1043A>G (p.Gln348Arg) n.493A>G | gnomAD v4 |
17 | g.41583561T>G | CA399476322 | KRT14 | c.1043A>C (p.Gln348Pro) n.493A>C | |
17 | g.41583562G>A | CA399476325 | KRT14 | c.1042C>T (p.Gln348Ter) n.492C>T | |
17 | g.41583562G>C | CA399476328 | KRT14 | c.1042C>G (p.Gln348Glu) n.492C>G | |
17 | g.41583562G>T | CA399476330 | KRT14 | c.1042C>A (p.Gln348Lys) n.492C>A | |
17 | g.41583563G>A | CA500205360 | KRT14 | c.1041C>T (p.Ser347=) n.491C>T | |
17 | g.41583563G>C | CA500205361 | KRT14 | c.1041C>G (p.Ser347=) n.491C>G | |
17 | g.41583563G>T | CA500205362 | KRT14 | c.1041C>A (p.Ser347=) n.491C>A | |
17 | g.41583564G>A | CA399476338 | KRT14 | c.1040C>T (p.Ser347Phe) n.490C>T | |
17 | g.41583564G>C | CA399476336 | KRT14 | c.1040C>G (p.Ser347Cys) n.490C>G | |
17 | g.41583564G>T | CA399476334 | KRT14 | c.1040C>A (p.Ser347Tyr) n.490C>A | |
17 | g.41583565A>C | CA399476341 | KRT14 | c.1039T>G (p.Ser347Ala) n.489T>G | |
17 | g.41583565A>G | CA399476344 | KRT14 | c.1039T>C (p.Ser347Pro) n.489T>C | gnomAD v4 |
17 | g.41583565A>T | CA399476346 | KRT14 | c.1039T>A (p.Ser347Thr) n.489T>A | |
17 | g.41583566C>A | CA399476350 | KRT14 | c.1038G>T (p.Gln346His) n.488G>T | |
17 | g.41583566C>G | CA399476352 | KRT14 | c.1038G>C (p.Gln346His) n.488G>C | gnomAD v4 |
17 | g.41583566C>T | CA500205363 | KRT14 | c.1038G>A (p.Gln346=) n.488G>A | |
17 | g.41583567T>A | CA399476356 | KRT14 | c.1037A>T (p.Gln346Leu) n.487A>T | |
17 | g.41583567T>C | CA399476358 | KRT14 | c.1037A>G (p.Gln346Arg) n.487A>G | |
17 | g.41583567T>G | CA399476360 | KRT14 | c.1037A>C (p.Gln346Pro) n.487A>C | |
17 | g.41583568G>A | CA399476368 | KRT14 | c.1036C>T (p.Gln346Ter) n.486C>T | |
17 | g.41583568G>C | CA399476371 | KRT14 | c.1036C>G (p.Gln346Glu) n.486C>G | |
17 | g.41583568G>T | CA399476373 | KRT14 | c.1036C>A (p.Gln346Lys) n.486C>A | |
17 | g.41583569C>A | CA500205366 | KRT14 | c.1035G>T (p.Leu345=) n.485G>T | gnomAD v4 |
17 | g.41583569C= | CA2260085458 | KRT14 | c.1035G= (p.Leu345=) n.485G= | |
17 | g.41583569C>G | CA500205364 | KRT14 | c.1035G>C (p.Leu345=) n.485G>C | |
17 | g.41583569C>T | CA500205365 | KRT14 | c.1035G>A (p.Leu345=) n.485G>A | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583570A>C | CA399476380 | KRT14 | c.1034T>G (p.Leu345Arg) n.484T>G | |
17 | g.41583570A>G | CA399476377 | KRT14 | c.1034T>C (p.Leu345Pro) n.484T>C | |
17 | g.41583570A>T | CA399476376 | KRT14 | c.1034T>A (p.Leu345Gln) n.484T>A | |
17 | g.41583571G>A | CA8562532 | KRT14 | c.1033C>T (p.Leu345=) n.483C>T | dbSNP ExAC gnomAD v2 |
17 | g.41583571G>C | CA399476385 | KRT14 | c.1033C>G (p.Leu345Val) n.483C>G | |
17 | g.41583571G= | CA2260085459 | KRT14 | c.1033C= (p.Leu345=) n.483C= | |
17 | g.41583571G>T | CA399476387 | KRT14 | c.1033C>A (p.Leu345Met) n.483C>A | |
17 | g.41583572C>A | CA399476390 | KRT14 | c.1032G>T (p.Glu344Asp) n.482G>T | |
17 | g.41583572C= | CA2260085460 | KRT14 | c.1032G= (p.Glu344=) n.482G= | |
17 | g.41583572C>G | CA399476392 | KRT14 | c.1032G>C (p.Glu344Asp) n.482G>C | gnomAD v4 |
17 | g.41583572C>T | CA8562533 | KRT14 | c.1032G>A (p.Glu344=) n.482G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583573T>A | CA399476397 | KRT14 | c.1031A>T (p.Glu344Val) n.481A>T | |
17 | g.41583573T>C | CA399476398 | KRT14 | c.1031A>G (p.Glu344Gly) n.481A>G | |
17 | g.41583573T>G | CA399476401 | KRT14 | c.1031A>C (p.Glu344Ala) n.481A>C | |
17 | g.41583574C>A | CA399476403 | KRT14 | c.1030G>T (p.Glu344Ter) n.480G>T | |
17 | g.41583574C= | CA2260085461 | KRT14 | c.1030G= (p.Glu344=) n.480G= | |
17 | g.41583574C>G | CA399476406 | KRT14 | c.1030G>C (p.Glu344Gln) n.480G>C | |
17 | g.41583574C>T | CA399476407 | KRT14 | c.1030G>A (p.Glu344Lys) n.480G>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583575A>C | CA399476410 | KRT14 | c.1029T>G (p.Ile343Met) n.479T>G | |
17 | g.41583575A>G | CA500205367 | KRT14 | c.1029T>C (p.Ile343=) n.479T>C | gnomAD v4 |
17 | g.41583575A>T | CA500205368 | KRT14 | c.1029T>A (p.Ile343=) n.479T>A | |
17 | g.41583576A>C | CA399476415 | KRT14 | c.1028T>G (p.Ile343Ser) n.478T>G | |
17 | g.41583576A>G | CA399476418 | KRT14 | c.1028T>C (p.Ile343Thr) n.478T>C | gnomAD v4 |
17 | g.41583576A>T | CA399476413 | KRT14 | c.1028T>A (p.Ile343Asn) n.478T>A | |
17 | g.41583577T>A | CA399476424 | KRT14 | c.1027A>T (p.Ile343Phe) n.477A>T | |
17 | g.41583577T>C | CA399476421 | KRT14 | c.1027A>G (p.Ile343Val) n.477A>G | |
17 | g.41583577T>G | CA399476426 | KRT14 | c.1027A>C (p.Ile343Leu) n.477A>C | |
17 | g.41583578C>A | CA399476428 | KRT14 | c.1026G>T (p.Glu342Asp) n.476G>T | |
17 | g.41583578C>G | CA399476429 | KRT14 | c.1026G>C (p.Glu342Asp) n.476G>C | |
17 | g.41583578C>T | CA500205369 | KRT14 | c.1026G>A (p.Glu342=) n.476G>A | |
17 | g.41583579T>A | CA399476433 | KRT14 | c.1025A>T (p.Glu342Val) n.475A>T | |
17 | g.41583579T>C | CA399476435 | KRT14 | c.1025A>G (p.Glu342Gly) n.475A>G | |
17 | g.41583579T>G | CA399476438 | KRT14 | c.1025A>C (p.Glu342Ala) n.475A>C | |
17 | g.41583580C>A | CA399476440 | KRT14 | c.1024G>T (p.Glu342Ter) n.474G>T | |
17 | g.41583580C= | CA2260085462 | KRT14 | c.1024G= (p.Glu342=) n.474G= | |
17 | g.41583580C>G | CA399476442 | KRT14 | c.1024G>C (p.Glu342Gln) n.474G>C | |
17 | g.41583580C>T | CA399476444 | KRT14 | c.1024G>A (p.Glu342Lys) n.474G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.41583581C>A | CA500205370 | KRT14 | c.1023G>T (p.Leu341=) n.473G>T | |
17 | g.41583581C>G | CA500205371 | KRT14 | c.1023G>C (p.Leu341=) n.473G>C | gnomAD v4 |
17 | g.41583581C>T | CA500205372 | KRT14 | c.1023G>A (p.Leu341=) n.473G>A | |
17 | g.41583582A>C | CA399476447 | KRT14 | c.1022T>G (p.Leu341Arg) n.472T>G | |
17 | g.41583582A>G | CA399476449 | KRT14 | c.1022T>C (p.Leu341Pro) n.472T>C | |
17 | g.41583582A>T | CA399476452 | KRT14 | c.1022T>A (p.Leu341Gln) n.472T>A | |
17 | g.41583583G>A | CA500205373 | KRT14 | c.1021C>T (p.Leu341=) n.471C>T | dbSNP gnomAD v4 |
17 | g.41583583G>C | CA8562534 | KRT14 | c.1021C>G (p.Leu341Val) n.471C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583583G= | CA2260085463 | KRT14 | c.1021C= (p.Leu341=) n.471C= | |
17 | g.41583583G>T | CA399476456 | KRT14 | c.1021C>A (p.Leu341Met) n.471C>A | dbSNP gnomAD v4 |
17 | g.41583584G>A | CA500205374 | KRT14 | c.1020C>T (p.Asn340=) n.470C>T | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583584G>C | CA399476459 | KRT14 | c.1020C>G (p.Asn340Lys) n.470C>G | |
17 | g.41583584G= | CA2260085464 | KRT14 | c.1020C= (p.Asn340=) n.470C= | |
17 | g.41583584G>T | CA8562535 | KRT14 | c.1020C>A (p.Asn340Lys) n.470C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583585T>A | CA399476463 | KRT14 | c.1019A>T (p.Asn340Ile) n.469A>T | dbSNP gnomAD v4 |
17 | g.41583585T>C | CA399476465 | KRT14 | c.1019A>G (p.Asn340Ser) n.469A>G | gnomAD v4 |
17 | g.41583585T>G | CA399476468 | KRT14 | c.1019A>C (p.Asn340Thr) n.469A>C | dbSNP |
17 | g.41583585T= | CA2260085465 | KRT14 | c.1019A= (p.Asn340=) n.469A= | |
17 | g.41583586T>A | CA399476471 | KRT14 | c.1018A>T (p.Asn340Tyr) n.468A>T | |
17 | g.41583586T>C | CA399476473 | KRT14 | c.1018A>G (p.Asn340Asp) n.468A>G | |
17 | g.41583586T>G | CA399476475 | KRT14 | c.1018A>C (p.Asn340His) n.468A>C | |
17 | g.41583587C>A | CA399476478 | KRT14 | c.1017G>T (p.Gln339His) n.467G>T | |
17 | g.41583587C>G | CA399476480 | KRT14 | c.1017G>C (p.Gln339His) n.467G>C | |
17 | g.41583587C>T | CA500205375 | KRT14 | c.1017G>A (p.Gln339=) n.467G>A | |
17 | g.41583588T>A | CA399476483 | KRT14 | c.1016A>T (p.Gln339Leu) n.466A>T | |
17 | g.41583588T>C | CA399476484 | KRT14 | c.1016A>G (p.Gln339Arg) n.466A>G | |
17 | g.41583588T>G | CA399476486 | KRT14 | c.1016A>C (p.Gln339Pro) n.466A>C | |
17 | g.41583589G>A | CA399476492 | KRT14 | c.1015C>T (p.Gln339Ter) n.465C>T | |
17 | g.41583589G>C | CA399476490 | KRT14 | c.1015C>G (p.Gln339Glu) n.465C>G | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583589G= | CA2260085466 | KRT14 | c.1015C= (p.Gln339=) n.465C= | |
17 | g.41583589G>T | CA399476489 | KRT14 | c.1015C>A (p.Gln339Lys) n.465C>A | |
17 | g.41583590C>A | CA399476496 | KRT14 | c.1014G>T (p.Met338Ile) n.464G>T | |
17 | g.41583590C= | CA2260085467 | KRT14 | c.1014G= (p.Met338=) n.464G= | |
17 | g.41583590C>G | CA399476498 | KRT14 | c.1014G>C (p.Met338Ile) n.464G>C | gnomAD v4 |
17 | g.41583590C>T | CA399476500 | KRT14 | c.1014G>A (p.Met338Ile) n.464G>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583591A= | CA2260085468 | KRT14 | c.1013T= (p.Met338=) n.463T= | |
17 | g.41583591A>C | CA8562536 | KRT14 | c.1013T>G (p.Met338Arg) n.463T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583591A>G | CA8562537 | KRT14 | c.1013T>C (p.Met338Thr) n.463T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583591A>T | CA399476507 | KRT14 | c.1013T>A (p.Met338Lys) n.463T>A | |
17 | g.41583592T>A | CA399476511 | KRT14 | c.1012A>T (p.Met338Leu) n.462A>T | |
17 | g.41583592T>C | CA399476513 | KRT14 | c.1012A>G (p.Met338Val) n.462A>G | dbSNP |
17 | g.41583592T>G | CA399476515 | KRT14 | c.1012A>C (p.Met338Leu) n.462A>C | |
17 | g.41583592_41583600delinsTGGTGCGCC | CA2260085469 | KRT14 | c.1004_1012delinsGGCGCACCA (p.Arg335=) n.454_462delinsGGCGCACCA | |
17 | g.41583593G>A | CA500205377 | KRT14 | c.1011C>T (p.Thr337=) n.461C>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583593G>C | CA8562538 | KRT14 | c.1011C>G (p.Thr337=) n.461C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583593G= | CA2260085471 | KRT14 | c.1011C= (p.Thr337=) n.461C= | |
17 | g.41583593G>T | CA500205376 | KRT14 | c.1011C>A (p.Thr337=) n.461C>A | |
17 | g.41583595_41583602del | CA2260085470 | KRT14 | c.1004_1011del (p.Arg335HisfsTer7) n.454_461del | dbSNP |
17 | g.41583594G>A | CA399476520 | KRT14 | c.1010C>T (p.Thr337Ile) n.460C>T | COSMIC |
17 | g.41583594G>C | CA399476523 | KRT14 | c.1010C>G (p.Thr337Ser) n.460C>G | |
17 | g.41583594G>T | CA399476526 | KRT14 | c.1010C>A (p.Thr337Asn) n.460C>A | |
17 | g.41583595T>A | CA399476533 | KRT14 | c.1009A>T (p.Thr337Ser) n.459A>T | COSMIC |
17 | g.41583595T>C | CA399476529 | KRT14 | c.1009A>G (p.Thr337Ala) n.459A>G | dbSNP gnomAD v4 |
17 | g.41583595T>G | CA399476531 | KRT14 | c.1009A>C (p.Thr337Pro) n.459A>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583595T= | CA2260085472 | KRT14 | c.1009A= (p.Thr337=) n.459A= | |
17 | g.41583596G>A | CA500205378 | KRT14 | c.1008C>T (p.Arg336=) n.458C>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583596G>C | CA500205379 | KRT14 | c.1008C>G (p.Arg336=) n.458C>G | |
17 | g.41583596G= | CA2260085473 | KRT14 | c.1008C= (p.Arg336=) n.458C= | |
17 | g.41583596G>T | CA500205380 | KRT14 | c.1008C>A (p.Arg336=) n.458C>A | |
17 | g.41583597C>A | CA399476534 | KRT14 | c.1007G>T (p.Arg336Leu) n.457G>T | |
17 | g.41583597C= | CA2260085474 | KRT14 | c.1007G= (p.Arg336=) n.457G= | |
17 | g.41583597C>G | CA399476536 | KRT14 | c.1007G>C (p.Arg336Pro) n.457G>C | dbSNP |
17 | g.41583597C>T | CA8562539 | KRT14 | c.1007G>A (p.Arg336His) n.457G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.41583598G>A | CA8562540 | KRT14 | c.1006C>T (p.Arg336Cys) n.456C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583598G>C | CA399476541 | KRT14 | c.1006C>G (p.Arg336Gly) n.456C>G | |
17 | g.41583598G= | CA2260085475 | KRT14 | c.1006C= (p.Arg336=) n.456C= | |
17 | g.41583598G>T | CA399476543 | KRT14 | c.1006C>A (p.Arg336Ser) n.456C>A | |
17 | g.41583599C>A | CA500205381 | KRT14 | c.1005G>T (p.Arg335=) n.455G>T | |
17 | g.41583599C>G | CA500205382 | KRT14 | c.1005G>C (p.Arg335=) n.455G>C | gnomAD v4 |
17 | g.41583599C>T | CA500205383 | KRT14 | c.1005G>A (p.Arg335=) n.455G>A | |
17 | g.41583600C>A | CA399476547 | KRT14 | c.1004G>T (p.Arg335Leu) n.454G>T | |
17 | g.41583600C= | CA2260085476 | KRT14 | c.1004G= (p.Arg335=) n.454G= | |
17 | g.41583600C>G | CA399476548 | KRT14 | c.1004G>C (p.Arg335Pro) n.454G>C | |
17 | g.41583600C>T | CA399476550 | KRT14 | c.1004G>A (p.Arg335Gln) n.454G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583601G>A | CA8562541 | KRT14 | c.1003C>T (p.Arg335Trp) n.453C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583601G>C | CA399476553 | KRT14 | c.1003C>G (p.Arg335Gly) n.453C>G | gnomAD v4 |
17 | g.41583601G= | CA2260085477 | KRT14 | c.1003C= (p.Arg335=) n.453C= | |
17 | g.41583601G>T | CA500205384 | KRT14 | c.1003C>A (p.Arg335=) n.453C>A | gnomAD v4 |
17 | g.41583602G>A | CA500205385 | KRT14 | c.1002C>T (p.Leu334=) n.452C>T | |
17 | g.41583602G>C | CA8562542 | KRT14 | c.1002C>G (p.Leu334=) n.452C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583602G= | CA2260085478 | KRT14 | c.1002C= (p.Leu334=) n.452C= | |
17 | g.41583602G>T | CA500205386 | KRT14 | c.1002C>A (p.Leu334=) n.452C>A | |
17 | g.41583603A>C | CA399476558 | KRT14 | c.1001T>G (p.Leu334Arg) n.451T>G | |
17 | g.41583603A>G | CA399476560 | KRT14 | c.1001T>C (p.Leu334Pro) n.451T>C | |
17 | g.41583603A>T | CA399476555 | KRT14 | c.1001T>A (p.Leu334His) n.451T>A | |
17 | g.41583604G>A | CA399476565 | KRT14 | c.1000C>T (p.Leu334Phe) n.450C>T | dbSNP gnomAD v4 |
17 | g.41583604G>C | CA399476563 | KRT14 | c.1000C>G (p.Leu334Val) n.450C>G | |
17 | g.41583604G= | CA2260085479 | KRT14 | c.1000C= (p.Leu334=) n.450C= | |
17 | g.41583604G>T | CA399476567 | KRT14 | c.1000C>A (p.Leu334Ile) n.450C>A | |
17 | g.41583605C>A | CA399476570 | KRT14 | c.999G>T (p.Glu333Asp) n.449G>T | |
17 | g.41583605C= | CA2260085480 | KRT14 | c.999G= (p.Glu333=) n.449G= | |
17 | g.41583605C>G | CA399476572 | KRT14 | c.999G>C (p.Glu333Asp) n.449G>C | |
17 | g.41583605C>T | CA500205387 | KRT14 | c.999G>A (p.Glu333=) n.449G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583606T>A | CA399476575 | KRT14 | c.998A>T (p.Glu333Val) n.448A>T | |
17 | g.41583606T>C | CA399476577 | KRT14 | c.998A>G (p.Glu333Gly) n.448A>G | |
17 | g.41583606T>G | CA399476579 | KRT14 | c.998A>C (p.Glu333Ala) n.448A>C | |
17 | g.41583607C>A | CA399476581 | KRT14 | c.997G>T (p.Glu333Ter) n.447G>T | |
17 | g.41583607C= | CA2260085481 | KRT14 | c.997G= (p.Glu333=) n.447G= | |
17 | g.41583607C>G | CA399476583 | KRT14 | c.997G>C (p.Glu333Gln) n.447G>C | dbSNP gnomAD v4 |
17 | g.41583607C>T | CA399476585 | KRT14 | c.997G>A (p.Glu333Lys) n.447G>A | |
17 | g.41583608C>A | CA500205388 | KRT14 | c.996G>T (p.Ser332=) n.446G>T | |
17 | g.41583608C= | CA2260085482 | KRT14 | c.996G= (p.Ser332=) n.446G= | |
17 | g.41583608C>G | CA500205389 | KRT14 | c.996G>C (p.Ser332=) n.446G>C | |
17 | g.41583608C>T | CA8562543 | KRT14 | c.996G>A (p.Ser332=) n.446G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583609G>A | CA8562544 | KRT14 | c.995C>T (p.Ser332Leu) n.445C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583609G>C | CA399476591 | KRT14 | c.995C>G (p.Ser332Trp) n.445C>G | |
17 | g.41583609G= | CA2260085483 | KRT14 | c.995C= (p.Ser332=) n.445C= | |
17 | g.41583609G>T | CA399476593 | KRT14 | c.995C>A (p.Ser332Ter) n.445C>A | gnomAD v4 |
17 | g.41583610A>C | CA399476601 | KRT14 | c.994T>G (p.Ser332Ala) n.444T>G | |
17 | g.41583610A>G | CA399476598 | KRT14 | c.994T>C (p.Ser332Pro) n.444T>C | |
17 | g.41583610A>T | CA399476596 | KRT14 | c.994T>A (p.Ser332Thr) n.444T>A | gnomAD v4 |
17 | g.41583611G>A | CA500205390 | KRT14 | c.993C>T (p.Ile331=) n.443C>T | |
17 | g.41583611G>C | CA399476603 | KRT14 | c.993C>G (p.Ile331Met) n.443C>G | |
17 | g.41583611G= | CA2260085484 | KRT14 | c.993C= (p.Ile331=) n.443C= | |
17 | g.41583611G>T | CA500205391 | KRT14 | c.993C>A (p.Ile331=) n.443C>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583612A>C | CA399476605 | KRT14 | c.992T>G (p.Ile331Ser) n.442T>G | |
17 | g.41583612A>G | CA399476607 | KRT14 | c.992T>C (p.Ile331Thr) n.442T>C | |
17 | g.41583612A>T | CA399476609 | KRT14 | c.992T>A (p.Ile331Asn) n.442T>A | |
17 | g.41583613T>A | CA399476613 | KRT14 | c.991A>T (p.Ile331Phe) n.441A>T | |
17 | g.41583613T>C | CA399476615 | KRT14 | c.991A>G (p.Ile331Val) n.441A>G | gnomAD v4 |
17 | g.41583613T>G | CA8562545 | KRT14 | c.991A>C (p.Ile331Leu) n.441A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583613T= | CA2260085485 | KRT14 | c.991A= (p.Ile331=) n.441A= | |
17 | g.41583614C>A | CA399476620 | KRT14 | c.990G>T (p.Glu330Asp) n.440G>T | |
17 | g.41583614C>G | CA399476622 | KRT14 | c.990G>C (p.Glu330Asp) n.440G>C | |
17 | g.41583614C>T | CA500205392 | KRT14 | c.990G>A (p.Glu330=) n.440G>A | |
17 | g.41583615T>A | CA399476625 | KRT14 | c.989A>T (p.Glu330Val) n.439A>T | |
17 | g.41583615T>C | CA399476627 | KRT14 | c.989A>G (p.Glu330Gly) n.439A>G | |
17 | g.41583615T>G | CA8562546 | KRT14 | c.989A>C (p.Glu330Ala) n.439A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583615T= | CA2260085486 | KRT14 | c.989A= (p.Glu330=) n.439A= | |
17 | g.41583616C>A | CA399476633 | KRT14 | c.988G>T (p.Glu330Ter) n.438G>T | |
17 | g.41583616C= | CA2260085487 | KRT14 | c.988G= (p.Glu330=) n.438G= | |
17 | g.41583616C>G | CA399476630 | KRT14 | c.988G>C (p.Glu330Gln) n.438G>C | |
17 | g.41583616C>T | CA8562547 | KRT14 | c.988G>A (p.Glu330Lys) n.438G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583617G>A | CA8562548 | KRT14 | c.987C>T (p.Ser329=) n.437C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583617G>C | CA399476639 | KRT14 | c.987C>G (p.Ser329Arg) n.437C>G | gnomAD v4 |
17 | g.41583617G= | CA2260085488 | KRT14 | c.987C= (p.Ser329=) n.437C= | |
17 | g.41583617G>T | CA399476636 | KRT14 | c.987C>A (p.Ser329Arg) n.437C>A | dbSNP gnomAD v4 |
17 | g.41583618C>A | CA399476641 | KRT14 | c.986G>T (p.Ser329Ile) n.436G>T | |
17 | g.41583618C= | CA2260085489 | KRT14 | c.986G= (p.Ser329=) n.436G= | |
17 | g.41583618C>G | CA399476642 | KRT14 | c.986G>C (p.Ser329Thr) n.436G>C | gnomAD v4 |
17 | g.41583618C>T | CA399476644 | KRT14 | c.986G>A (p.Ser329Asn) n.436G>A | dbSNP |
17 | g.41583619T>A | CA399476647 | KRT14 | c.985A>T (p.Ser329Cys) n.435A>T | |
17 | g.41583619T>C | CA399476649 | KRT14 | c.985A>G (p.Ser329Gly) n.435A>G | gnomAD v4 |
17 | g.41583619T>G | CA399476651 | KRT14 | c.985A>C (p.Ser329Arg) n.435A>C | |
17 | g.41583620C>A | CA399476652 | KRT14 | c.984G>T (p.Lys328Asn) n.434G>T | |
17 | g.41583620C>G | CA399476654 | KRT14 | c.984G>C (p.Lys328Asn) n.434G>C | |
17 | g.41583620C>T | CA500205393 | KRT14 | c.984G>A (p.Lys328=) n.434G>A | ClinVar |
17 | g.41583621T>A | CA399476659 | KRT14 | c.983A>T (p.Lys328Met) n.433A>T | |
17 | g.41583621T>C | CA399476660 | KRT14 | c.983A>G (p.Lys328Arg) n.433A>G | |
17 | g.41583621T>G | CA399476663 | KRT14 | c.983A>C (p.Lys328Thr) n.433A>C | |
17 | g.41583622T>A | CA399476671 | KRT14 | c.982A>T (p.Lys328Ter) n.432A>T | |
17 | g.41583622T>C | CA399476669 | KRT14 | c.982A>G (p.Lys328Glu) n.432A>G | |
17 | g.41583622T>G | CA399476667 | KRT14 | c.982A>C (p.Lys328Gln) n.432A>C | |
17 | g.41583623G>A | CA500205394 | KRT14 | c.981C>T (p.Gly327=) n.431C>T | |
17 | g.41583623G>C | CA500205395 | KRT14 | c.981C>G (p.Gly327=) n.431C>G | gnomAD v4 |
17 | g.41583623G>T | CA500205396 | KRT14 | c.981C>A (p.Gly327=) n.431C>A | |
17 | g.41583624C>A | CA399476673 | KRT14 | c.980G>T (p.Gly327Val) n.430G>T | |
17 | g.41583624C>G | CA399476675 | KRT14 | c.980G>C (p.Gly327Ala) n.430G>C | |
17 | g.41583624C>T | CA399476676 | KRT14 | c.980G>A (p.Gly327Asp) n.430G>A | |
17 | g.41583625C>A | CA399476678 | KRT14 | c.979G>T (p.Gly327Cys) n.429G>T | |
17 | g.41583625C= | CA2260085490 | KRT14 | c.979G= (p.Gly327=) n.429G= | |
17 | g.41583625C>G | CA399476680 | KRT14 | c.979G>C (p.Gly327Arg) n.429G>C | |
17 | g.41583625C>T | CA8562549 | KRT14 | c.979G>A (p.Gly327Ser) n.429G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |