Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.151674498T>A | CA429243035 | NEB | c.3966A>T (p.Ala1322=) | |
2 | g.151674498T>C | CA429243036 | NEB | c.3966A>G (p.Ala1322=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.151674498T>G | CA429243037 | NEB | c.3966A>C (p.Ala1322=) | |
2 | g.151674498T= | CA1298292925 | NEB | c.3966A= (p.Ala1322=) | |
2 | g.151674499G>A | CA348817660 | NEB | c.3965C>T (p.Ala1322Val) | |
2 | g.151674499G>C | CA348817661 | NEB | c.3965C>G (p.Ala1322Gly) | |
2 | g.151674499G>T | CA348817662 | NEB | c.3965C>A (p.Ala1322Glu) | |
2 | g.151674500C>A | CA1910778 | NEB | c.3964G>T (p.Ala1322Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.151674500C= | CA1298292930 | NEB | c.3964G= (p.Ala1322=) | |
2 | g.151674500C>G | CA348817663 | NEB | c.3964G>C (p.Ala1322Pro) | |
2 | g.151674500C>T | CA348817664 | NEB | c.3964G>A (p.Ala1322Thr) | |
2 | g.151674501C>A | CA348817666 | NEB | c.3963G>T (p.Lys1321Asn) | |
2 | g.151674501C>G | CA348817665 | NEB | c.3963G>C (p.Lys1321Asn) | |
2 | g.151674501C>T | CA429243039 | NEB | c.3963G>A (p.Lys1321=) | |
2 | g.151674502T>A | CA348817667 | NEB | c.3962A>T (p.Lys1321Met) | |
2 | g.151674502T>C | CA1910779 | NEB | c.3962A>G (p.Lys1321Arg) | dbSNP ExAC |
2 | g.151674502T>G | CA348817668 | NEB | c.3962A>C (p.Lys1321Thr) | |
2 | g.151674502T= | CA1298292937 | NEB | c.3962A= (p.Lys1321=) | |
2 | g.151674503T>A | CA348817669 | NEB | c.3961A>T (p.Lys1321Ter) | |
2 | g.151674503T>C | CA348817670 | NEB | c.3961A>G (p.Lys1321Glu) | |
2 | g.151674503T>G | CA348817671 | NEB | c.3961A>C (p.Lys1321Gln) | |
2 | g.151674504G>A | CA429243043 | NEB | c.3960C>T (p.Ala1320=) | |
2 | g.151674504G>C | CA429243045 | NEB | c.3960C>G (p.Ala1320=) | |
2 | g.151674504G>T | CA429243046 | NEB | c.3960C>A (p.Ala1320=) | |
2 | g.151674505G>A | CA348817674 | NEB | c.3959C>T (p.Ala1320Val) | gnomAD v4 |
2 | g.151674505G>C | CA348817672 | NEB | c.3959C>G (p.Ala1320Gly) | |
2 | g.151674505G>T | CA348817673 | NEB | c.3959C>A (p.Ala1320Asp) | |
2 | g.151674506C>A | CA348817675 | NEB | c.3958G>T (p.Ala1320Ser) | |
2 | g.151674506C>G | CA348817676 | NEB | c.3958G>C (p.Ala1320Pro) | |
2 | g.151674506C>T | CA348817677 | NEB | c.3958G>A (p.Ala1320Thr) | |
2 | g.151674507T>A | CA429243048 | NEB | c.3957A>T (p.Ala1319=) | |
2 | g.151674507T>C | CA429243049 | NEB | c.3957A>G (p.Ala1319=) | |
2 | g.151674507T>G | CA429243050 | NEB | c.3957A>C (p.Ala1319=) | |
2 | g.151674508G>A | CA348817678 | NEB | c.3956C>T (p.Ala1319Val) | |
2 | g.151674508G>C | CA348817679 | NEB | c.3956C>G (p.Ala1319Gly) | |
2 | g.151674508G>T | CA348817680 | NEB | c.3956C>A (p.Ala1319Glu) | |
2 | g.151674509C>A | CA348817681 | NEB | c.3955G>T (p.Ala1319Ser) | gnomAD v4 |
2 | g.151674509C>G | CA348817682 | NEB | c.3955G>C (p.Ala1319Pro) | |
2 | g.151674509C>T | CA348817683 | NEB | c.3955G>A (p.Ala1319Thr) | |
2 | g.151674510A>C | CA429243052 | NEB | c.3954T>G (p.Thr1318=) | |
2 | g.151674510A>G | CA429243053 | NEB | c.3954T>C (p.Thr1318=) | ClinVar dbSNP |
2 | g.151674510A>T | CA429243054 | NEB | c.3954T>A (p.Thr1318=) | gnomAD v4 |
2 | g.151674511G>A | CA348817684 | NEB | c.3953C>T (p.Thr1318Ile) | |
2 | g.151674511G>C | CA348817685 | NEB | c.3953C>G (p.Thr1318Ser) | |
2 | g.151674511G>T | CA348817686 | NEB | c.3953C>A (p.Thr1318Asn) | |
2 | g.151674512T>A | CA348817687 | NEB | c.3952A>T (p.Thr1318Ser) | |
2 | g.151674512T>C | CA348817689 | NEB | c.3952A>G (p.Thr1318Ala) | |
2 | g.151674512T>G | CA348817688 | NEB | c.3952A>C (p.Thr1318Pro) | |
2 | g.151674513G>A | CA429243059 | NEB | c.3951C>T (p.Ile1317=) | |
2 | g.151674513G>C | CA348817690 | NEB | c.3951C>G (p.Ile1317Met) |