Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.44305055T>A | CA444230898 | FGF10 | c.567A>T (p.Gly189=) | |
5 | g.44305055T>C | CA444230899 | FGF10 | c.567A>G (p.Gly189=) | |
5 | g.44305055T>G | CA444230900 | FGF10 | c.567A>C (p.Gly189=) | |
5 | g.44305056C>A | CA359697599 | FGF10 | c.566G>T (p.Gly189Val) | |
5 | g.44305056C>G | CA359697600 | FGF10 | c.566G>C (p.Gly189Ala) | |
5 | g.44305056C>T | CA359697601 | FGF10 | c.566G>A (p.Gly189Glu) | |
5 | g.44305057C>A | CA359697602 | FGF10 | c.565G>T (p.Gly189Ter) | COSMIC |
5 | g.44305057C>G | CA359697603 | FGF10 | c.565G>C (p.Gly189Arg) | |
5 | g.44305057C>T | CA359697604 | FGF10 | c.565G>A (p.Gly189Arg) | |
5 | g.44305058T>A | CA359697606 | FGF10 | c.564A>T (p.Arg188Ser) | |
5 | g.44305058T>C | CA444230901 | FGF10 | c.564A>G (p.Arg188=) | dbSNP |
5 | g.44305058T>G | CA359697605 | FGF10 | c.564A>C (p.Arg188Ser) | |
5 | g.44305059C>A | CA118160545 | FGF10 | c.563G>T (p.Arg188Ile) | dbSNP |
5 | g.44305059C= | CA1543079510 | FGF10 | c.563G= (p.Arg188=) | |
5 | g.44305059C>G | CA359697607 | FGF10 | c.563G>C (p.Arg188Thr) | gnomAD v4 |
5 | g.44305059C>T | CA359697608 | FGF10 | c.563G>A (p.Arg188Lys) | |
5 | g.44305060T>A | CA359697609 | FGF10 | c.562A>T (p.Arg188Ter) | |
5 | g.44305060T>C | CA359697610 | FGF10 | c.562A>G (p.Arg188Gly) | |
5 | g.44305060T>G | CA444230902 | FGF10 | c.562A>C (p.Arg188=) | |
5 | g.44305061C>A | CA359697611 | FGF10 | c.561G>T (p.Arg187Ser) | |
5 | g.44305061C>G | CA359697612 | FGF10 | c.561G>C (p.Arg187Ser) | |
5 | g.44305061C>T | CA444230903 | FGF10 | c.561G>A (p.Arg187=) | COSMIC |
5 | g.44305062C>A | CA359697613 | FGF10 | c.560G>T (p.Arg187Met) | |
5 | g.44305062C= | CA1543079512 | FGF10 | c.560G= (p.Arg187=) | |
5 | g.44305062C>G | CA359697614 | FGF10 | c.560G>C (p.Arg187Thr) | |
5 | g.44305062C>T | CA359697615 | FGF10 | c.560G>A (p.Arg187Lys) | dbSNP |
5 | g.44305063T>A | CA359697616 | FGF10 | c.559A>T (p.Arg187Trp) | |
5 | g.44305063T>C | CA359697617 | FGF10 | c.559A>G (p.Arg187Gly) | |
5 | g.44305063T>G | CA444230904 | FGF10 | c.559A>C (p.Arg187=) | |
5 | g.44305064T>A | CA444230907 | FGF10 | c.558A>T (p.Pro186=) | |
5 | g.44305064T>C | CA444230905 | FGF10 | c.558A>G (p.Pro186=) | |
5 | g.44305064T>G | CA444230906 | FGF10 | c.558A>C (p.Pro186=) | dbSNP |
5 | g.44305064T= | CA1543079518 | FGF10 | c.558A= (p.Pro186=) | |
5 | g.44305065G>A | CA359697620 | FGF10 | c.557C>T (p.Pro186Leu) | |
5 | g.44305065G>C | CA359697619 | FGF10 | c.557C>G (p.Pro186Arg) | |
5 | g.44305065G>T | CA359697618 | FGF10 | c.557C>A (p.Pro186Gln) | COSMIC |
5 | g.44305066G>A | CA359697621 | FGF10 | c.556C>T (p.Pro186Ser) | |
5 | g.44305066G>C | CA359697622 | FGF10 | c.556C>G (p.Pro186Ala) | |
5 | g.44305066G>T | CA359697623 | FGF10 | c.556C>A (p.Pro186Thr) | |
5 | g.44305067A>C | CA444230909 | FGF10 | c.555T>G (p.Ala185=) | |
5 | g.44305067A>G | CA444230911 | FGF10 | c.555T>C (p.Ala185=) | |
5 | g.44305067A>T | CA444230910 | FGF10 | c.555T>A (p.Ala185=) | |
5 | g.44305068G>A | CA118160546 | FGF10 | c.554C>T (p.Ala185Val) | dbSNP |
5 | g.44305068G>C | CA359697624 | FGF10 | c.554C>G (p.Ala185Gly) | |
5 | g.44305068G= | CA1543079523 | FGF10 | c.554C= (p.Ala185=) | |
5 | g.44305068G>T | CA359697625 | FGF10 | c.554C>A (p.Ala185Asp) | |
5 | g.44305069C>A | CA359697626 | FGF10 | c.553G>T (p.Ala185Ser) | |
5 | g.44305069C= | CA1543079528 | FGF10 | c.553G= (p.Ala185=) | |
5 | g.44305069C>G | CA359697627 | FGF10 | c.553G>C (p.Ala185Pro) | |
5 | g.44305069C>T | CA359697628 | FGF10 | c.553G>A (p.Ala185Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |