| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41586412_41586473del | CA645584614 | KRT14 | c.362_423del (p.Asn121ArgfsTer8) | COSMIC |
| 17 | g.41586466_41586467delinsGC | CA2739267536 | KRT14 | c.368_369delinsGC (p.Asn123Ser) | ClinVar |
| 17 | g.41586467T>A | CA399482536 | KRT14 | c.368A>T (p.Asn123Ile) | |
| 17 | g.41586467T>C | CA216911 | KRT14 | c.368A>G (p.Asn123Ser) | ClinVar dbSNP |
| 17 | g.41586467T>G | CA399482537 | KRT14 | c.368A>C (p.Asn123Thr) | |
| 17 | g.41586467T= | CA2260086835 | KRT14 | c.368A= (p.Asn123=) | |
| 17 | g.41586468T>A | CA399482540 | KRT14 | c.367A>T (p.Asn123Tyr) | |
| 17 | g.41586468T>C | CA399482541 | KRT14 | c.367A>G (p.Asn123Asp) | |
| 17 | g.41586468T>G | CA399482542 | KRT14 | c.367A>C (p.Asn123His) | |
| 17 | g.41586469G>A | CA499992002 | KRT14 | c.366C>T (p.Leu122=) | COSMIC |
| 17 | g.41586469G>C | CA499992003 | KRT14 | c.366C>G (p.Leu122=) | |
| 17 | g.41586469G>T | CA499992004 | KRT14 | c.366C>A (p.Leu122=) | |
| 17 | g.41586470A>C | CA399482545 | KRT14 | c.365T>G (p.Leu122Arg) | |
| 17 | g.41586470A>G | CA399482548 | KRT14 | c.365T>C (p.Leu122Pro) | |
| 17 | g.41586470A>T | CA399482546 | KRT14 | c.365T>A (p.Leu122His) | |
| 17 | g.41586471G>A | CA216909 | KRT14 | c.364C>T (p.Leu122Phe) | ClinVar dbSNP gnomAD v4 |
| 17 | g.41586471G>C | CA399482550 | KRT14 | c.364C>G (p.Leu122Val) | |
| 17 | g.41586471G= | CA2260086836 | KRT14 | c.364C= (p.Leu122=) | |
| 17 | g.41586471G>T | CA399482552 | KRT14 | c.364C>A (p.Leu122Ile) | |
| 17 | g.41586472G>A | CA8562734 | KRT14 | c.363C>T (p.Asn121=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41586472G>C | CA399482554 | KRT14 | c.363C>G (p.Asn121Lys) | |
| 17 | g.41586472G= | CA2260086837 | KRT14 | c.363C= (p.Asn121=) | |
| 17 | g.41586472G>T | CA399482556 | KRT14 | c.363C>A (p.Asn121Lys) | |
| 17 | g.41586473T>A | CA399482558 | KRT14 | c.362A>T (p.Asn121Ile) | |
| 17 | g.41586473T>C | CA399482560 | KRT14 | c.362A>G (p.Asn121Ser) | dbSNP gnomAD v4 |
| 17 | g.41586473T>G | CA399482562 | KRT14 | c.362A>C (p.Asn121Thr) | |
| 17 | g.41586473T= | CA2260086838 | KRT14 | c.362A= (p.Asn121=) | |
| 17 | g.41586474_41586480del | CA2637837296 | KRT14 | c.356_362del (p.Met119ThrfsTer25) | gnomAD v4 |
| 17 | g.41586474T>A | CA399482565 | KRT14 | c.361A>T (p.Asn121Tyr) | |
| 17 | g.41586474T>C | CA399482567 | KRT14 | c.361A>G (p.Asn121Asp) | |
| 17 | g.41586474T>G | CA399482564 | KRT14 | c.361A>C (p.Asn121His) | |
| 17 | g.41586475C>A | CA399482569 | KRT14 | c.360G>T (p.Gln120His) | |
| 17 | g.41586475C>G | CA399482571 | KRT14 | c.360G>C (p.Gln120His) | |
| 17 | g.41586475C>T | CA499992006 | KRT14 | c.360G>A (p.Gln120=) | |
| 17 | g.41586476T>A | CA399482573 | KRT14 | c.359A>T (p.Gln120Leu) | |
| 17 | g.41586476T>C | CA216907 | KRT14 | c.359A>G (p.Gln120Arg) | ClinVar dbSNP |
| 17 | g.41586476T>G | CA216905 | KRT14 | c.359A>C (p.Gln120Pro) | ClinVar dbSNP |
| 17 | g.41586476T= | CA2260086839 | KRT14 | c.359A= (p.Gln120=) | |
| 17 | g.41586477G>A | CA399482580 | KRT14 | c.358C>T (p.Gln120Ter) | |
| 17 | g.41586477G>C | CA399482578 | KRT14 | c.358C>G (p.Gln120Glu) | |
| 17 | g.41586477G>T | CA399482576 | KRT14 | c.358C>A (p.Gln120Lys) | |
| 17 | g.41586478C>A | CA399482581 | KRT14 | c.357G>T (p.Met119Ile) | |
| 17 | g.41586478C= | CA2260086840 | KRT14 | c.357G= (p.Met119=) | |
| 17 | g.41586478C>G | CA399482582 | KRT14 | c.357G>C (p.Met119Ile) | |
| 17 | g.41586478C>T | CA216903 | KRT14 | c.357G>A (p.Met119Ile) | ClinVar dbSNP |
| 17 | g.41586479A= | CA2260086841 | KRT14 | c.356T= (p.Met119=) | |
| 17 | g.41586479A>C | CA399482585 | KRT14 | c.356T>G (p.Met119Arg) | ClinVar dbSNP |
| 17 | g.41586479A>G | CA216901 | KRT14 | c.356T>C (p.Met119Thr) | ClinVar dbSNP |
| 17 | g.41586479A>T | CA399482586 | KRT14 | c.356T>A (p.Met119Lys) | |
| 17 | g.41586480T>A | CA399482589 | KRT14 | c.355A>T (p.Met119Leu) |