Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.86510794C>A | CA119646 | FOXF1 | c.225C>A (p.Tyr75Ter) | ClinVar dbSNP COSMIC COSMIC |
16 | g.86510794C= | CA2239913446 | FOXF1 | c.225C= (p.Tyr75=) | |
16 | g.86510794C>G | CA397005578 | FOXF1 | c.225C>G (p.Tyr75Ter) | |
16 | g.86510794C>T | CA497013812 | FOXF1 | c.225C>T (p.Tyr75=) | |
16 | g.86510795C>A | CA397005584 | FOXF1 | c.226C>A (p.Gln76Lys) | |
16 | g.86510795C>G | CA397005580 | FOXF1 | c.226C>G (p.Gln76Glu) | |
16 | g.86510795C>T | CA397005582 | FOXF1 | c.226C>T (p.Gln76Ter) | |
16 | g.86510796A= | CA2239913447 | FOXF1 | c.227A= (p.Gln76=) | |
16 | g.86510796A>C | CA397005586 | FOXF1 | c.227A>C (p.Gln76Pro) | |
16 | g.86510796A>G | CA397005588 | FOXF1 | c.227A>G (p.Gln76Arg) | |
16 | g.86510796A>T | CA397005589 | FOXF1 | c.227A>T (p.Gln76Leu) | dbSNP gnomAD v4 |
16 | g.86510797G>A | CA8217373 | FOXF1 | c.228G>A (p.Gln76=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.86510797G>C | CA397005591 | FOXF1 | c.228G>C (p.Gln76His) | |
16 | g.86510797G= | CA2239913448 | FOXF1 | c.228G= (p.Gln76=) | |
16 | g.86510797G>T | CA397005592 | FOXF1 | c.228G>T (p.Gln76His) | gnomAD v4 |
16 | g.86510798T>A | CA397005594 | FOXF1 | c.229T>A (p.Phe77Ile) | |
16 | g.86510798T>C | CA397005596 | FOXF1 | c.229T>C (p.Phe77Leu) | |
16 | g.86510798T>G | CA397005597 | FOXF1 | c.229T>G (p.Phe77Val) | |
16 | g.86510799T>A | CA397005601 | FOXF1 | c.230T>A (p.Phe77Tyr) | |
16 | g.86510799T>C | CA397005602 | FOXF1 | c.230T>C (p.Phe77Ser) | |
16 | g.86510799T>G | CA397005604 | FOXF1 | c.230T>G (p.Phe77Cys) | |
16 | g.86510800C>A | CA397005608 | FOXF1 | c.231C>A (p.Phe77Leu) | |
16 | g.86510800C= | CA2239913449 | FOXF1 | c.231C= (p.Phe77=) | |
16 | g.86510800C>G | CA397005607 | FOXF1 | c.231C>G (p.Phe77Leu) | |
16 | g.86510800C>T | CA8217374 | FOXF1 | c.231C>T (p.Phe77=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
16 | g.86510801C>A | CA397005613 | FOXF1 | c.232C>A (p.Leu78Met) | |
16 | g.86510801C= | CA2239913450 | FOXF1 | c.232C= (p.Leu78=) | |
16 | g.86510801C>G | CA397005610 | FOXF1 | c.232C>G (p.Leu78Val) | |
16 | g.86510801C>T | CA497013824 | FOXF1 | c.232C>T (p.Leu78=) | dbSNP |
16 | g.86510802T>A | CA397005615 | FOXF1 | c.233T>A (p.Leu78Gln) | |
16 | g.86510802T>C | CA397005617 | FOXF1 | c.233T>C (p.Leu78Pro) | |
16 | g.86510802T>G | CA397005618 | FOXF1 | c.233T>G (p.Leu78Arg) | |
16 | g.86510803G>A | CA497013828 | FOXF1 | c.234G>A (p.Leu78=) | gnomAD v4 |
16 | g.86510803G>C | CA497013830 | FOXF1 | c.234G>C (p.Leu78=) | |
16 | g.86510803G>T | CA497013831 | FOXF1 | c.234G>T (p.Leu78=) | |
16 | g.86510804C>A | CA397005620 | FOXF1 | c.235C>A (p.Gln79Lys) | COSMIC |
16 | g.86510804C>G | CA397005622 | FOXF1 | c.235C>G (p.Gln79Glu) | gnomAD v4 |
16 | g.86510804C>T | CA397005623 | FOXF1 | c.235C>T (p.Gln79Ter) | |
16 | g.86510804_86510806delinsCAG | CA2239913451 | FOXF1 | c.235_237delinsCAG (p.Gln79=) | |
16 | g.86510805A= | CA2239913453 | FOXF1 | c.236A= (p.Gln79=) | |
16 | g.86510805A>C | CA397005625 | FOXF1 | c.236A>C (p.Gln79Pro) | |
16 | g.86510805A>G | CA397005627 | FOXF1 | c.236A>G (p.Gln79Arg) | dbSNP |
16 | g.86510805A>T | CA397005629 | FOXF1 | c.236A>T (p.Gln79Leu) | |
16 | g.86510807_86510808del | CA2239913452 | FOXF1 | c.238_239del (p.Ser80ProfsTer?) | ClinVar dbSNP |
16 | g.86510806G>A | CA497013834 | FOXF1 | c.237G>A (p.Gln79=) | |
16 | g.86510806G>C | CA397005631 | FOXF1 | c.237G>C (p.Gln79His) | COSMIC COSMIC |
16 | g.86510806G>T | CA397005632 | FOXF1 | c.237G>T (p.Gln79His) | |
16 | g.86510807A>C | CA397005636 | FOXF1 | c.238A>C (p.Ser80Arg) | |
16 | g.86510807A>G | CA397005638 | FOXF1 | c.238A>G (p.Ser80Gly) | |
16 | g.86510807A>T | CA397005634 | FOXF1 | c.238A>T (p.Ser80Cys) |