Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583829C>A | CA399477414 | KRT14 | c.858G>T (p.Glu286Asp) n.308G>T | |
17 | g.41583829C>G | CA399477415 | KRT14 | c.858G>C (p.Glu286Asp) n.308G>C | |
17 | g.41583829C>T | CA500205547 | KRT14 | c.858G>A (p.Glu286=) n.308G>A | |
17 | g.41583830T>A | CA399477418 | KRT14 | c.857A>T (p.Glu286Val) n.307A>T | |
17 | g.41583830T>C | CA399477420 | KRT14 | c.857A>G (p.Glu286Gly) n.307A>G | dbSNP |
17 | g.41583830T>G | CA399477422 | KRT14 | c.857A>C (p.Glu286Ala) n.307A>C | |
17 | g.41583831C>A | CA399477425 | KRT14 | c.856G>T (p.Glu286Ter) n.306G>T | COSMIC |
17 | g.41583831C= | CA2260085585 | KRT14 | c.856G= (p.Glu286=) n.306G= | |
17 | g.41583831C>G | CA8562590 | KRT14 | c.856G>C (p.Glu286Gln) n.306G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583831C>T | CA399477428 | KRT14 | c.856G>A (p.Glu286Lys) n.306G>A | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.41583832G>A | CA8562591 | KRT14 | c.855C>T (p.Asn285=) n.305C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583832G>C | CA399477435 | KRT14 | c.855C>G (p.Asn285Lys) n.305C>G | gnomAD v4 |
17 | g.41583832G= | CA2260085586 | KRT14 | c.855C= (p.Asn285=) n.305C= | |
17 | g.41583832G>T | CA399477432 | KRT14 | c.855C>A (p.Asn285Lys) n.305C>A | COSMIC |
17 | g.41583833T>A | CA399477440 | KRT14 | c.854A>T (p.Asn285Ile) n.304A>T | |
17 | g.41583833T>C | CA399477441 | KRT14 | c.854A>G (p.Asn285Ser) n.304A>G | |
17 | g.41583833T>G | CA399477442 | KRT14 | c.854A>C (p.Asn285Thr) n.304A>C | ClinVar |
17 | g.41583834T>A | CA399477443 | KRT14 | c.853A>T (p.Asn285Tyr) n.303A>T | |
17 | g.41583834T>C | CA399477444 | KRT14 | c.853A>G (p.Asn285Asp) n.303A>G | |
17 | g.41583834T>G | CA399477445 | KRT14 | c.853A>C (p.Asn285His) n.303A>C | |
17 | g.41583835C>A | CA500205552 | KRT14 | c.852G>T (p.Leu284=) n.302G>T | |
17 | g.41583835C>G | CA500205553 | KRT14 | c.852G>C (p.Leu284=) n.302G>C | |
17 | g.41583835C>T | CA500205554 | KRT14 | c.852G>A (p.Leu284=) n.302G>A | |
17 | g.41583836A>C | CA399477446 | KRT14 | c.851T>G (p.Leu284Arg) n.301T>G | |
17 | g.41583836A>G | CA399477447 | KRT14 | c.851T>C (p.Leu284Pro) n.301T>C | ClinVar dbSNP |
17 | g.41583836A>T | CA399477448 | KRT14 | c.851T>A (p.Leu284Gln) n.301T>A | |
17 | g.41583837G>A | CA500205555 | KRT14 | c.850C>T (p.Leu284=) n.300C>T | |
17 | g.41583837G>C | CA399477449 | KRT14 | c.850C>G (p.Leu284Val) n.300C>G | |
17 | g.41583837G>T | CA399477450 | KRT14 | c.850C>A (p.Leu284Met) n.300C>A | |
17 | g.41583838A>C | CA399477451 | KRT14 | c.849T>G (p.Ile283Met) n.299T>G | |
17 | g.41583838A>G | CA500205560 | KRT14 | c.849T>C (p.Ile283=) n.299T>C | |
17 | g.41583838A>T | CA500205557 | KRT14 | c.849T>A (p.Ile283=) n.299T>A | |
17 | g.41583839A= | CA2260085587 | KRT14 | c.848T= (p.Ile283=) n.298T= | |
17 | g.41583839A>C | CA399477453 | KRT14 | c.848T>G (p.Ile283Ser) n.298T>G | |
17 | g.41583839A>G | CA399477454 | KRT14 | c.848T>C (p.Ile283Thr) n.298T>C | dbSNP |
17 | g.41583839A>T | CA399477452 | KRT14 | c.848T>A (p.Ile283Asn) n.298T>A | |
17 | g.41583840T>A | CA399477455 | KRT14 | c.847A>T (p.Ile283Phe) n.297A>T | |
17 | g.41583840T>C | CA399477456 | KRT14 | c.847A>G (p.Ile283Val) n.297A>G | |
17 | g.41583840T>G | CA399477457 | KRT14 | c.847A>C (p.Ile283Leu) n.297A>C | |
17 | g.41583841G>A | CA500205570 | KRT14 | c.846C>T (p.Arg282=) n.296C>T | |
17 | g.41583841G>C | CA500205566 | KRT14 | c.846C>G (p.Arg282=) n.296C>G | |
17 | g.41583841G>T | CA500205567 | KRT14 | c.846C>A (p.Arg282=) n.296C>A | |
17 | g.41583842C>A | CA8562593 | KRT14 | c.845G>T (p.Arg282Leu) n.295G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583842C= | CA2260085588 | KRT14 | c.845G= (p.Arg282=) n.295G= | |
17 | g.41583842C>G | CA399477458 | KRT14 | c.845G>C (p.Arg282Pro) n.295G>C | |
17 | g.41583842C>T | CA8562592 | KRT14 | c.845G>A (p.Arg282His) n.295G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583843G>A | CA8562594 | KRT14 | c.844C>T (p.Arg282Cys) n.294C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583843G>C | CA399477460 | KRT14 | c.844C>G (p.Arg282Gly) n.294C>G | gnomAD v4 |
17 | g.41583843G= | CA2260085589 | KRT14 | c.844C= (p.Arg282=) n.294C= | |
17 | g.41583843G>T | CA399477462 | KRT14 | c.844C>A (p.Arg282Ser) n.294C>A | |
17 | g.41583844G>A | CA500205580 | KRT14 | c.843C>T (p.Ser281=) n.293C>T | gnomAD v4 |
17 | g.41583844G>C | CA399477463 | KRT14 | c.843C>G (p.Ser281Arg) n.293C>G | |
17 | g.41583844G>T | CA399477464 | KRT14 | c.843C>A (p.Ser281Arg) n.293C>A | |
17 | g.41583845C>A | CA399477465 | KRT14 | c.842G>T (p.Ser281Ile) n.292G>T | |
17 | g.41583845C>G | CA399477466 | KRT14 | c.842G>C (p.Ser281Thr) n.292G>C | |
17 | g.41583845C>T | CA399477467 | KRT14 | c.842G>A (p.Ser281Asn) n.292G>A | |
17 | g.41583846T>A | CA399477468 | KRT14 | c.841A>T (p.Ser281Cys) n.291A>T | |
17 | g.41583846T>C | CA399477470 | KRT14 | c.841A>G (p.Ser281Gly) n.291A>G | |
17 | g.41583846T>G | CA399477469 | KRT14 | c.841A>C (p.Ser281Arg) n.291A>C | |
17 | g.41583847C>A | CA500205585 | KRT14 | c.840G>T (p.Leu280=) n.290G>T | |
17 | g.41583847C>G | CA500205586 | KRT14 | c.840G>C (p.Leu280=) n.290G>C | gnomAD v4 |
17 | g.41583847C>T | CA500205588 | KRT14 | c.840G>A (p.Leu280=) n.290G>A | gnomAD v4 |
17 | g.41583848A>C | CA399477471 | KRT14 | c.839T>G (p.Leu280Arg) n.289T>G | |
17 | g.41583848A>G | CA399477472 | KRT14 | c.839T>C (p.Leu280Pro) n.289T>C | |
17 | g.41583848A>T | CA399477473 | KRT14 | c.839T>A (p.Leu280Gln) n.289T>A | |
17 | g.41583849G>A | CA500205594 | KRT14 | c.838C>T (p.Leu280=) n.288C>T | |
17 | g.41583849G>C | CA399477474 | KRT14 | c.838C>G (p.Leu280Val) n.288C>G | |
17 | g.41583849G= | CA2260085590 | KRT14 | c.838C= (p.Leu280=) n.288C= | |
17 | g.41583849G>T | CA8562595 | KRT14 | c.838C>A (p.Leu280Met) n.288C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583850G>A | CA500205597 | KRT14 | c.837C>T (p.Asp279=) n.287C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583850G>C | CA399477475 | KRT14 | c.837C>G (p.Asp279Glu) n.287C>G | |
17 | g.41583850G= | CA2260085591 | KRT14 | c.837C= (p.Asp279=) n.287C= | |
17 | g.41583850G>T | CA399477476 | KRT14 | c.837C>A (p.Asp279Glu) n.287C>A | |
17 | g.41583851T>A | CA399477477 | KRT14 | c.836A>T (p.Asp279Val) n.286A>T | |
17 | g.41583851T>C | CA399477478 | KRT14 | c.836A>G (p.Asp279Gly) n.286A>G | |
17 | g.41583851T>G | CA399477479 | KRT14 | c.836A>C (p.Asp279Ala) n.286A>C | |
17 | g.41583852C>A | CA399477480 | KRT14 | c.835G>T (p.Asp279Tyr) n.285G>T | |
17 | g.41583852C>G | CA399477481 | KRT14 | c.835G>C (p.Asp279His) n.285G>C | |
17 | g.41583852C>T | CA399477482 | KRT14 | c.835G>A (p.Asp279Asn) n.285G>A | |
17 | g.41583853C>A | CA500205608 | KRT14 | c.834G>T (p.Val278=) n.284G>T | |
17 | g.41583853C>G | CA500205606 | KRT14 | c.834G>C (p.Val278=) n.284G>C | |
17 | g.41583853C>T | CA500205607 | KRT14 | c.834G>A (p.Val278=) n.284G>A | COSMIC |
17 | g.41583854A>C | CA399477487 | KRT14 | c.833T>G (p.Val278Gly) n.283T>G | |
17 | g.41583854A>G | CA399477489 | KRT14 | c.833T>C (p.Val278Ala) n.283T>C | |
17 | g.41583854A>T | CA399477484 | KRT14 | c.833T>A (p.Val278Glu) n.283T>A | |
17 | g.41583855C>A | CA399477492 | KRT14 | c.832G>T (p.Val278Leu) n.282G>T | gnomAD v4 |
17 | g.41583855C= | CA2260085592 | KRT14 | c.832G= (p.Val278=) n.282G= | |
17 | g.41583855C>G | CA8562596 | KRT14 | c.832G>C (p.Val278Leu) n.282G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583855C>T | CA8562597 | KRT14 | c.832G>A (p.Val278Met) n.282G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583856G>A | CA8562598 | KRT14 | c.831C>T (p.Gly277=) n.281C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583856G>C | CA500205613 | KRT14 | c.831C>G (p.Gly277=) n.281C>G | |
17 | g.41583856G= | CA2260085593 | KRT14 | c.831C= (p.Gly277=) n.281C= | |
17 | g.41583856G>T | CA500205614 | KRT14 | c.831C>A (p.Gly277=) n.281C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583857C>A | CA399477500 | KRT14 | c.830G>T (p.Gly277Val) n.280G>T | ClinVar dbSNP |
17 | g.41583857C>G | CA399477502 | KRT14 | c.830G>C (p.Gly277Ala) n.280G>C | |
17 | g.41583857C>T | CA399477504 | KRT14 | c.830G>A (p.Gly277Asp) n.280G>A | |
17 | g.41583858C>A | CA399477507 | KRT14 | c.829G>T (p.Gly277Cys) n.279G>T | |
17 | g.41583858C>G | CA399477509 | KRT14 | c.829G>C (p.Gly277Arg) n.279G>C | |
17 | g.41583858C>T | CA399477512 | KRT14 | c.829G>A (p.Gly277Ser) n.279G>A | |
17 | g.41583859A>C | CA500205620 | KRT14 | c.828T>G (p.Pro276=) n.278T>G | |
17 | g.41583859A>G | CA500205621 | KRT14 | c.828T>C (p.Pro276=) n.278T>C | gnomAD v4 |
17 | g.41583859A>T | CA500205623 | KRT14 | c.828T>A (p.Pro276=) n.278T>A | |
17 | g.41583859_41583860delinsAG | CA2260085594 | KRT14 | c.827_828delinsCT (p.Pro276=) n.277_278delinsCT | |
17 | g.41583860G>A | CA399477515 | KRT14 | c.827C>T (p.Pro276Leu) n.277C>T | |
17 | g.41583860G>C | CA399477520 | KRT14 | c.827C>G (p.Pro276Arg) n.277C>G | |
17 | g.41583860G>T | CA399477518 | KRT14 | c.827C>A (p.Pro276His) n.277C>A | |
17 | g.41583861del | CA8562599 | KRT14 | c.827del (p.Pro276LeufsTer5) n.277del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583861G>A | CA399477524 | KRT14 | c.826C>T (p.Pro276Ser) n.276C>T | gnomAD v4 |
17 | g.41583861G>C | CA399477526 | KRT14 | c.826C>G (p.Pro276Ala) n.276C>G | |
17 | g.41583861G>T | CA399477528 | KRT14 | c.826C>A (p.Pro276Thr) n.276C>A | |
17 | g.41583862T>A | CA500205629 | KRT14 | c.825A>T (p.Ala275=) n.275A>T | |
17 | g.41583862T>C | CA500205627 | KRT14 | c.825A>G (p.Ala275=) n.275A>G | |
17 | g.41583862T>G | CA500205628 | KRT14 | c.825A>C (p.Ala275=) n.275A>C | dbSNP gnomAD v4 |
17 | g.41583862T= | CA2260085595 | KRT14 | c.825A= (p.Ala275=) n.275A= | |
17 | g.41583863G>A | CA399477536 | KRT14 | c.824C>T (p.Ala275Val) n.274C>T | COSMIC |
17 | g.41583863G>C | CA399477532 | KRT14 | c.824C>G (p.Ala275Gly) n.274C>G | |
17 | g.41583863G>T | CA399477534 | KRT14 | c.824C>A (p.Ala275Glu) n.274C>A | |
17 | g.41583864C>A | CA399477539 | KRT14 | c.823G>T (p.Ala275Ser) n.273G>T | |
17 | g.41583864C>G | CA399477541 | KRT14 | c.823G>C (p.Ala275Pro) n.273G>C | |
17 | g.41583864C>T | CA399477543 | KRT14 | c.823G>A (p.Ala275Thr) n.273G>A | |
17 | g.41583865A>C | CA500205638 | KRT14 | c.822T>G (p.Ala274=) n.272T>G | |
17 | g.41583865A>G | CA500205640 | KRT14 | c.822T>C (p.Ala274=) n.272T>C | gnomAD v4 |
17 | g.41583865A>T | CA500205641 | KRT14 | c.822T>A (p.Ala274=) n.272T>A | |
17 | g.41583866G>A | CA399477547 | KRT14 | c.821C>T (p.Ala274Val) n.271C>T | |
17 | g.41583866G>C | CA399477549 | KRT14 | c.821C>G (p.Ala274Gly) n.271C>G | |
17 | g.41583866G= | CA2260085596 | KRT14 | c.821C= (p.Ala274=) n.271C= | |
17 | g.41583866G>T | CA216986 | KRT14 | c.821C>A (p.Ala274Asp) n.271C>A | ClinVar dbSNP |
17 | g.41583867C>A | CA399477554 | KRT14 | c.820G>T (p.Ala274Ser) n.270G>T | |
17 | g.41583867C= | CA2260085597 | KRT14 | c.820G= (p.Ala274=) n.270G= | |
17 | g.41583867C>G | CA399477556 | KRT14 | c.820G>C (p.Ala274Pro) n.270G>C | |
17 | g.41583867C>T | CA8562600 | KRT14 | c.820G>A (p.Ala274Thr) n.270G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583868G>A | CA8562601 | KRT14 | c.819C>T (p.Asp273=) n.269C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583868G>C | CA399477565 | KRT14 | c.819C>G (p.Asp273Glu) n.269C>G | dbSNP gnomAD v4 |
17 | g.41583868G= | CA2260085598 | KRT14 | c.819C= (p.Asp273=) n.269C= | |
17 | g.41583868G>T | CA399477567 | KRT14 | c.819C>A (p.Asp273Glu) n.269C>A | |
17 | g.41583869T>A | CA399477570 | KRT14 | c.818A>T (p.Asp273Val) n.268A>T | |
17 | g.41583869T>C | CA216984 | KRT14 | c.818A>G (p.Asp273Gly) n.268A>G | ClinVar dbSNP |
17 | g.41583869T>G | CA399477572 | KRT14 | c.818A>C (p.Asp273Ala) n.268A>C | |
17 | g.41583869T= | CA2260085599 | KRT14 | c.818A= (p.Asp273=) n.268A= | |
17 | g.41583870C>A | CA399477576 | KRT14 | c.817G>T (p.Asp273Tyr) n.267G>T | |
17 | g.41583870C= | CA2260085600 | KRT14 | c.817G= (p.Asp273=) n.267G= | |
17 | g.41583870C>G | CA399477577 | KRT14 | c.817G>C (p.Asp273His) n.267G>C | gnomAD v4 |
17 | g.41583870C>T | CA399477578 | KRT14 | c.817G>A (p.Asp273Asn) n.267G>A | dbSNP gnomAD v4 COSMIC |
17 | g.41583871C>A | CA399477582 | KRT14 | c.816G>T (p.Met272Ile) n.266G>T | |
17 | g.41583871C>G | CA399477584 | KRT14 | c.816G>C (p.Met272Ile) n.266G>C | |
17 | g.41583871C>T | CA399477586 | KRT14 | c.816G>A (p.Met272Ile) n.266G>A | |
17 | g.41583880_41583893del | CA2637835339 | KRT14 | c.803_816del (p.Val268GlyfsTer17) n.253_266del | gnomAD v4 |
17 | g.41583872A= | CA2260085601 | KRT14 | c.815T= (p.Met272=) n.265T= | |
17 | g.41583872A>C | CA216982 | KRT14 | c.815T>G (p.Met272Arg) n.265T>G | ClinVar dbSNP |
17 | g.41583872A>G | CA216980 | KRT14 | c.815T>C (p.Met272Thr) n.265T>C | ClinVar dbSNP |
17 | g.41583872A>T | CA399477592 | KRT14 | c.815T>A (p.Met272Lys) n.265T>A | ClinVar |
17 | g.41583873T>A | CA399477596 | KRT14 | c.814A>T (p.Met272Leu) n.264A>T | |
17 | g.41583873T>C | CA399477598 | KRT14 | c.814A>G (p.Met272Val) n.264A>G | |
17 | g.41583873T>G | CA399477600 | KRT14 | c.814A>C (p.Met272Leu) n.264A>C | |
17 | g.41583874C>A | CA399477605 | KRT14 | c.813G>T (p.Glu271Asp) n.263G>T | |
17 | g.41583874C>G | CA399477603 | KRT14 | c.813G>C (p.Glu271Asp) n.263G>C | |
17 | g.41583874C>T | CA500205655 | KRT14 | c.813G>A (p.Glu271=) n.263G>A | |
17 | g.41583875T>A | CA399477608 | KRT14 | c.812A>T (p.Glu271Val) n.262A>T | |
17 | g.41583875T>C | CA399477610 | KRT14 | c.812A>G (p.Glu271Gly) n.262A>G | |
17 | g.41583875T>G | CA399477612 | KRT14 | c.812A>C (p.Glu271Ala) n.262A>C | |
17 | g.41583876C>A | CA399477615 | KRT14 | c.811G>T (p.Glu271Ter) n.261G>T | |
17 | g.41583876C>G | CA399477618 | KRT14 | c.811G>C (p.Glu271Gln) n.261G>C | |
17 | g.41583876C>T | CA399477619 | KRT14 | c.811G>A (p.Glu271Lys) n.261G>A | |
17 | g.41583877C>A | CA500205662 | KRT14 | c.810G>T (p.Val270=) n.260G>T | |
17 | g.41583877C>G | CA500205664 | KRT14 | c.810G>C (p.Val270=) n.260G>C | |
17 | g.41583877C>T | CA500205665 | KRT14 | c.810G>A (p.Val270=) n.260G>A | |
17 | g.41583878A>C | CA399477623 | KRT14 | c.809T>G (p.Val270Gly) n.259T>G | |
17 | g.41583878A>G | CA399477625 | KRT14 | c.809T>C (p.Val270Ala) n.259T>C | |
17 | g.41583878A>T | CA399477627 | KRT14 | c.809T>A (p.Val270Glu) n.259T>A | |
17 | g.41583879C>A | CA399477629 | KRT14 | c.808G>T (p.Val270Leu) n.258G>T | |
17 | g.41583879C= | CA2260085602 | KRT14 | c.808G= (p.Val270=) n.258G= | |
17 | g.41583879C>G | CA399477631 | KRT14 | c.808G>C (p.Val270Leu) n.258G>C | |
17 | g.41583879C>T | CA216978 | KRT14 | c.808G>A (p.Val270Met) n.258G>A | ClinVar dbSNP |
17 | g.41583880A= | CA2260085603 | KRT14 | c.807T= (p.Asn269=) n.257T= | |
17 | g.41583880A>C | CA399477635 | KRT14 | c.807T>G (p.Asn269Lys) n.257T>G | |
17 | g.41583880A>G | CA8562602 | KRT14 | c.807T>C (p.Asn269=) n.257T>C | dbSNP ExAC gnomAD v2 |
17 | g.41583880A>T | CA399477634 | KRT14 | c.807T>A (p.Asn269Lys) n.257T>A | |
17 | g.41583881T>A | CA399477636 | KRT14 | c.806A>T (p.Asn269Ile) n.256A>T | |
17 | g.41583881T>C | CA399477637 | KRT14 | c.806A>G (p.Asn269Ser) n.256A>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583881T>G | CA399477638 | KRT14 | c.806A>C (p.Asn269Thr) n.256A>C | |
17 | g.41583881T= | CA2260085604 | KRT14 | c.806A= (p.Asn269=) n.256A= | |
17 | g.41583882T>A | CA399477639 | KRT14 | c.805A>T (p.Asn269Tyr) n.255A>T | |
17 | g.41583882T>C | CA399477640 | KRT14 | c.805A>G (p.Asn269Asp) n.255A>G | |
17 | g.41583882T>G | CA399477641 | KRT14 | c.805A>C (p.Asn269His) n.255A>C | |
17 | g.41583883G>A | CA500205678 | KRT14 | c.804C>T (p.Val268=) n.254C>T | |
17 | g.41583883G>C | CA500205680 | KRT14 | c.804C>G (p.Val268=) n.254C>G | |
17 | g.41583883G>T | CA500205679 | KRT14 | c.804C>A (p.Val268=) n.254C>A | COSMIC |
17 | g.41583884A= | CA2260085605 | KRT14 | c.803T= (p.Val268=) n.253T= | |
17 | g.41583884A>C | CA399477643 | KRT14 | c.803T>G (p.Val268Gly) n.253T>G | |
17 | g.41583884A>G | CA399477642 | KRT14 | c.803T>C (p.Val268Ala) n.253T>C | ClinVar |
17 | g.41583884A>T | CA216976 | KRT14 | c.803T>A (p.Val268Asp) n.253T>A | ClinVar dbSNP |
17 | g.41583885C>A | CA399477644 | KRT14 | c.802G>T (p.Val268Phe) n.252G>T | |
17 | g.41583885C= | CA2260085606 | KRT14 | c.802G= (p.Val268=) n.252G= | |
17 | g.41583885C>G | CA399477645 | KRT14 | c.802G>C (p.Val268Leu) n.252G>C | |
17 | g.41583885C>T | CA399477646 | KRT14 | c.802G>A (p.Val268Ile) n.252G>A | dbSNP |
17 | g.41583886A= | CA2260085607 | KRT14 | c.801T= (p.Asp267=) n.251T= | |
17 | g.41583886A>C | CA399477647 | KRT14 | c.801T>G (p.Asp267Glu) n.251T>G | |
17 | g.41583886A>G | CA8562603 | KRT14 | c.801T>C (p.Asp267=) n.251T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583886A>T | CA399477648 | KRT14 | c.801T>A (p.Asp267Glu) n.251T>A | |
17 | g.41583887T>A | CA399477649 | KRT14 | c.800A>T (p.Asp267Val) n.250A>T | |
17 | g.41583887T>C | CA399477651 | KRT14 | c.800A>G (p.Asp267Gly) n.250A>G | |
17 | g.41583887T>G | CA399477650 | KRT14 | c.800A>C (p.Asp267Ala) n.250A>C | |
17 | g.41583888C>A | CA399477652 | KRT14 | c.799G>T (p.Asp267Tyr) n.249G>T | |
17 | g.41583888C= | CA2260085608 | KRT14 | c.799G= (p.Asp267=) n.249G= | |
17 | g.41583888C>G | CA399477653 | KRT14 | c.799G>C (p.Asp267His) n.249G>C | gnomAD v4 |
17 | g.41583888C>T | CA290665037 | KRT14 | c.799G>A (p.Asp267Asn) n.249G>A | dbSNP |
17 | g.41583889T>A | CA500205696 | KRT14 | c.798A>T (p.Gly266=) n.248A>T | |
17 | g.41583889T>C | CA500205697 | KRT14 | c.798A>G (p.Gly266=) n.248A>G | |
17 | g.41583889T>G | CA500205701 | KRT14 | c.798A>C (p.Gly266=) n.248A>C | |
17 | g.41583890C>A | CA399477654 | KRT14 | c.797G>T (p.Gly266Val) n.247G>T | gnomAD v4 |
17 | g.41583890C>G | CA399477655 | KRT14 | c.797G>C (p.Gly266Ala) n.247G>C | |
17 | g.41583890C>T | CA399477656 | KRT14 | c.797G>A (p.Gly266Glu) n.247G>A | |
17 | g.41583891C>A | CA399477657 | KRT14 | c.796G>T (p.Gly266Ter) n.246G>T | |
17 | g.41583891C>G | CA399477658 | KRT14 | c.796G>C (p.Gly266Arg) n.246G>C | |
17 | g.41583891C>T | CA399477659 | KRT14 | c.796G>A (p.Gly266Arg) n.246G>A | gnomAD v4 COSMIC |
17 | g.41583892A>C | CA500205705 | KRT14 | c.795T>G (p.Gly265=) n.245T>G | |
17 | g.41583892A>G | CA500205706 | KRT14 | c.795T>C (p.Gly265=) n.245T>C | |
17 | g.41583892A>T | CA500205707 | KRT14 | c.795T>A (p.Gly265=) n.245T>A | |
17 | g.41583893C>A | CA399477660 | KRT14 | c.794G>T (p.Gly265Val) n.244G>T | |
17 | g.41583893C>G | CA399477661 | KRT14 | c.794G>C (p.Gly265Ala) n.244G>C | |
17 | g.41583893C>T | CA399477662 | KRT14 | c.794G>A (p.Gly265Asp) n.244G>A | |
17 | g.41583894C>A | CA399477663 | KRT14 | c.793G>T (p.Gly265Cys) n.243G>T | |
17 | g.41583894C= | CA2260085609 | KRT14 | c.793G= (p.Gly265=) n.243G= | |
17 | g.41583894C>G | CA399477665 | KRT14 | c.793G>C (p.Gly265Arg) n.243G>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583894C>T | CA399477664 | KRT14 | c.793G>A (p.Gly265Ser) n.243G>A | gnomAD v4 |
17 | g.41583895C>A | CA500205715 | KRT14 | c.792G>T (p.Val264=) n.242G>T | |
17 | g.41583895C= | CA2260085610 | KRT14 | c.792G= (p.Val264=) n.242G= | |
17 | g.41583895C>G | CA500205716 | KRT14 | c.792G>C (p.Val264=) n.242G>C | |
17 | g.41583895C>T | CA8562604 | KRT14 | c.792G>A (p.Val264=) n.242G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583896A>C | CA399477666 | KRT14 | c.791T>G (p.Val264Gly) n.241T>G | gnomAD v4 |
17 | g.41583896A>G | CA399477667 | KRT14 | c.791T>C (p.Val264Ala) n.241T>C | |
17 | g.41583896A>T | CA399477668 | KRT14 | c.791T>A (p.Val264Glu) n.241T>A | |
17 | g.41583897C>A | CA399477669 | KRT14 | c.790G>T (p.Val264Leu) n.240G>T | |
17 | g.41583897C= | CA2260085611 | KRT14 | c.790G= (p.Val264=) n.240G= | |
17 | g.41583897C>G | CA399477670 | KRT14 | c.790G>C (p.Val264Leu) n.240G>C | |
17 | g.41583897C>T | CA8562605 | KRT14 | c.790G>A (p.Val264Met) n.240G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583898C>A | CA399477671 | KRT14 | c.789G>T (p.Gln263His) n.239G>T | COSMIC |
17 | g.41583898C>G | CA399477672 | KRT14 | c.789G>C (p.Gln263His) n.239G>C | |
17 | g.41583898C>T | CA500205719 | KRT14 | c.789G>A (p.Gln263=) n.239G>A | |
17 | g.41583899T>A | CA399477673 | KRT14 | c.788A>T (p.Gln263Leu) n.238A>T | |
17 | g.41583899T>C | CA399477674 | KRT14 | c.788A>G (p.Gln263Arg) n.238A>G | dbSNP gnomAD v4 |
17 | g.41583899T>G | CA399477675 | KRT14 | c.788A>C (p.Gln263Pro) n.238A>C | |
17 | g.41583899T= | CA2260085612 | KRT14 | c.788A= (p.Gln263=) n.238A= | |
17 | g.41583900G>A | CA399477678 | KRT14 | c.787C>T (p.Gln263Ter) n.237C>T | gnomAD v4 |
17 | g.41583900G>C | CA399477676 | KRT14 | c.787C>G (p.Gln263Glu) n.237C>G | |
17 | g.41583900G>T | CA399477677 | KRT14 | c.787C>A (p.Gln263Lys) n.237C>A | |
17 | g.41583901G>A | CA8562606 | KRT14 | c.786C>T (p.Gly262=) n.236C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583901G>C | CA500205724 | KRT14 | c.786C>G (p.Gly262=) n.236C>G | |
17 | g.41583901G= | CA2260085613 | KRT14 | c.786C= (p.Gly262=) n.236C= | |
17 | g.41583901G>T | CA500205725 | KRT14 | c.786C>A (p.Gly262=) n.236C>A | |
17 | g.41583902C>A | CA399477679 | KRT14 | c.785G>T (p.Gly262Val) n.235G>T | |
17 | g.41583902C>G | CA399477680 | KRT14 | c.785G>C (p.Gly262Ala) n.235G>C | |
17 | g.41583902C>T | CA399477681 | KRT14 | c.785G>A (p.Gly262Asp) n.235G>A | |
17 | g.41583903C>A | CA399477682 | KRT14 | c.784G>T (p.Gly262Cys) n.234G>T | |
17 | g.41583903C= | CA2260085614 | KRT14 | c.784G= (p.Gly262=) n.234G= | |
17 | g.41583903C>G | CA399477683 | KRT14 | c.784G>C (p.Gly262Arg) n.234G>C | |
17 | g.41583903C>T | CA8562607 | KRT14 | c.784G>A (p.Gly262Ser) n.234G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583904T>A | CA399477684 | KRT14 | c.783A>T (p.Arg261Ser) n.233A>T | |
17 | g.41583904T>C | CA500205728 | KRT14 | c.783A>G (p.Arg261=) n.233A>G | dbSNP |
17 | g.41583904T>G | CA399477685 | KRT14 | c.783A>C (p.Arg261Ser) n.233A>C | |
17 | g.41583904T= | CA2260085615 | KRT14 | c.783A= (p.Arg261=) n.233A= | |
17 | g.41583905C>A | CA399477686 | KRT14 | c.782G>T (p.Arg261Ile) n.232G>T | |
17 | g.41583905C= | CA2260085616 | KRT14 | c.782G= (p.Arg261=) n.232G= | |
17 | g.41583905C>G | CA399477687 | KRT14 | c.782G>C (p.Arg261Thr) n.232G>C | dbSNP |
17 | g.41583905C>T | CA399477688 | KRT14 | c.782G>A (p.Arg261Lys) n.232G>A | |
17 | g.41583906T>A | CA399477689 | KRT14 | c.781A>T (p.Arg261Ter) n.231A>T | |
17 | g.41583906T>C | CA399477690 | KRT14 | c.781A>G (p.Arg261Gly) n.231A>G | |
17 | g.41583906T>G | CA500205730 | KRT14 | c.781A>C (p.Arg261=) n.231A>C | |
17 | g.41583907C>A | CA500205731 | KRT14 | c.780G>T (p.Leu260=) n.230G>T | |
17 | g.41583907C>G | CA500205733 | KRT14 | c.780G>C (p.Leu260=) n.230G>C | gnomAD v4 COSMIC |
17 | g.41583907C>T | CA500205732 | KRT14 | c.780G>A (p.Leu260=) n.230G>A | |
17 | g.41583908A= | CA2260085617 | KRT14 | c.779T= (p.Leu260=) n.229T= | |
17 | g.41583908A>C | CA399477691 | KRT14 | c.779T>G (p.Leu260Arg) n.229T>G | |
17 | g.41583908A>G | CA399477693 | KRT14 | c.779T>C (p.Leu260Pro) n.229T>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583908A>T | CA399477692 | KRT14 | c.779T>A (p.Leu260Gln) n.229T>A | |
17 | g.41583909G>A | CA500205737 | KRT14 | c.778C>T (p.Leu260=) n.228C>T | gnomAD v4 |
17 | g.41583909G>C | CA399477694 | KRT14 | c.778C>G (p.Leu260Val) n.228C>G | |
17 | g.41583909G= | CA2260085618 | KRT14 | c.778C= (p.Leu260=) n.228C= | |
17 | g.41583909G>T | CA399477695 | KRT14 | c.778C>A (p.Leu260Met) n.228C>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583910G>A | CA500205743 | KRT14 | c.777C>T (p.Ala259=) n.227C>T | |
17 | g.41583910G>C | CA500205739 | KRT14 | c.777C>G (p.Ala259=) n.227C>G | |
17 | g.41583910G>T | CA500205741 | KRT14 | c.777C>A (p.Ala259=) n.227C>A | |
17 | g.41583911G>A | CA399477696 | KRT14 | c.776C>T (p.Ala259Val) n.226C>T | dbSNP |
17 | g.41583911G>C | CA399477698 | KRT14 | c.776C>G (p.Ala259Gly) n.226C>G | |
17 | g.41583911G= | CA2260085619 | KRT14 | c.776C= (p.Ala259=) n.226C= | |
17 | g.41583911G>T | CA399477697 | KRT14 | c.776C>A (p.Ala259Asp) n.226C>A | |
17 | g.41583912C>A | CA399477699 | KRT14 | c.775G>T (p.Ala259Ser) n.225G>T | |
17 | g.41583912C>G | CA399477700 | KRT14 | c.775G>C (p.Ala259Pro) n.225G>C | gnomAD v4 |
17 | g.41583912C>T | CA399477701 | KRT14 | c.775G>A (p.Ala259Thr) n.225G>A | COSMIC |
17 | g.41583913A>C | CA399477702 | KRT14 | c.774T>G (p.Asn258Lys) n.224T>G | |
17 | g.41583913A>G | CA500205747 | KRT14 | c.774T>C (p.Asn258=) n.224T>C | |
17 | g.41583913A>T | CA399477703 | KRT14 | c.774T>A (p.Asn258Lys) n.224T>A | gnomAD v4 |
17 | g.41583914T>A | CA399477704 | KRT14 | c.773A>T (p.Asn258Ile) n.223A>T | gnomAD v4 |
17 | g.41583914T>C | CA399477705 | KRT14 | c.773A>G (p.Asn258Ser) n.223A>G | |
17 | g.41583914T>G | CA399477706 | KRT14 | c.773A>C (p.Asn258Thr) n.223A>C | |
17 | g.41583915T>A | CA399477707 | KRT14 | c.772A>T (p.Asn258Tyr) n.222A>T | |
17 | g.41583915T>C | CA399477708 | KRT14 | c.772A>G (p.Asn258Asp) n.222A>G | |
17 | g.41583915T>G | CA399477709 | KRT14 | c.772A>C (p.Asn258His) n.222A>C | |
17 | g.41583916C>A | CA399477711 | KRT14 | c.771G>T (p.Met257Ile) n.221G>T | |
17 | g.41583916C= | CA2260085620 | KRT14 | c.771G= (p.Met257=) n.221G= | |
17 | g.41583916C>G | CA399477710 | KRT14 | c.771G>C (p.Met257Ile) n.221G>C | |
17 | g.41583916C>T | CA290665046 | KRT14 | c.771G>A (p.Met257Ile) n.221G>A | dbSNP |
17 | g.41583917A= | CA2260085621 | KRT14 | c.770T= (p.Met257=) n.220T= | |
17 | g.41583917A>C | CA399477712 | KRT14 | c.770T>G (p.Met257Arg) n.220T>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583917A>G | CA8562608 | KRT14 | c.770T>C (p.Met257Thr) n.220T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583917A>T | CA399477713 | KRT14 | c.770T>A (p.Met257Lys) n.220T>A | dbSNP |
17 | g.41583918T>A | CA399477714 | KRT14 | c.769A>T (p.Met257Leu) n.219A>T | |
17 | g.41583918T>C | CA399477715 | KRT14 | c.769A>G (p.Met257Val) n.219A>G | |
17 | g.41583918T>G | CA399477716 | KRT14 | c.769A>C (p.Met257Leu) n.219A>C | |
17 | g.41583919C>A | CA399477717 | KRT14 | c.768G>T (p.Glu256Asp) n.218G>T | |
17 | g.41583919C>G | CA399477718 | KRT14 | c.768G>C (p.Glu256Asp) n.218G>C | |
17 | g.41583919C>T | CA500205748 | KRT14 | c.768G>A (p.Glu256=) n.218G>A | |
17 | g.41583920T>A | CA399477719 | KRT14 | c.767A>T (p.Glu256Val) n.217A>T | gnomAD v4 |
17 | g.41583920T>C | CA399477720 | KRT14 | c.767A>G (p.Glu256Gly) n.217A>G | |
17 | g.41583920T>G | CA399477721 | KRT14 | c.767A>C (p.Glu256Ala) n.217A>C | |
17 | g.41583921C>A | CA8562609 | KRT14 | c.766G>T (p.Glu256Ter) n.216G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583921C= | CA2260085622 | KRT14 | c.766G= (p.Glu256=) n.216G= | |
17 | g.41583921C>G | CA399477723 | KRT14 | c.766G>C (p.Glu256Gln) n.216G>C | dbSNP |
17 | g.41583921C>T | CA399477722 | KRT14 | c.766G>A (p.Glu256Lys) n.216G>A | |
17 | g.41583922C>A | CA399477724 | KRT14 | c.766-1G>T (n.766-1G>T) n.216-1G>T | |
17 | g.41583922C>G | CA399477725 | KRT14 | c.766-1G>C (n.766-1G>C) n.216-1G>C | |
17 | g.41583922C>T | CA399477726 | KRT14 | c.766-1G>A (n.766-1G>A) n.216-1G>A | |
17 | g.41583923T>A | CA399477727 | KRT14 | c.766-2A>T (n.766-2A>T) n.216-2A>T | COSMIC |
17 | g.41583923T>C | CA399477728 | KRT14 | c.766-2A>G (n.766-2A>G) n.216-2A>G | |
17 | g.41583923T>G | CA399477729 | KRT14 | c.766-2A>C (n.766-2A>C) n.216-2A>C | |
17 | g.41583924G>C | CA772039261 | KRT14 | c.766-3C>G (n.766-3C>G) n.216-3C>G | dbSNP |
17 | g.41583924G= | CA2260085623 | KRT14 | c.766-3C= (n.766-3C=) n.216-3C= | |
17 | g.41583924G>T | CA8562610 | KRT14 | c.766-3C>A (n.766-3C>A) n.216-3C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583927_41583931dup | CA2637835395 | KRT14 | c.766-10_766-6dup (n.766-10_766-6dup) n.216-10_216-6dup | gnomAD v4 |