Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.35285008A= | CA2333586133 | HAMP | c.221A= (p.His74=) n.2492A= | |
19 | g.35285008A>C | CA405301629 | HAMP | c.221A>C (p.His74Pro) n.2492A>C | |
19 | g.35285008A>G | CA9375832 | HAMP | c.221A>G (p.His74Arg) n.2492A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35285008A>T | CA405301633 | HAMP | c.221A>T (p.His74Leu) n.2492A>T | |
19 | g.35285009T>A | CA405301639 | HAMP | c.222T>A (p.His74Gln) n.2493T>A | |
19 | g.35285009T>C | CA507041708 | HAMP | c.222T>C (p.His74=) n.2493T>C | |
19 | g.35285009T>G | CA405301640 | HAMP | c.222T>G (p.His74Gln) n.2493T>G | |
19 | g.35285010C>A | CA507041711 | HAMP | c.223C>A (p.Arg75=) n.2494C>A | |
19 | g.35285010C= | CA2333586134 | HAMP | c.223C= (p.Arg75=) n.2494C= | |
19 | g.35285010C>G | CA405301644 | HAMP | c.223C>G (p.Arg75Gly) n.2494C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.35285010C>T | CA9375833 | HAMP | c.223C>T (p.Arg75Ter) n.2494C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35285011G>A | CA9375834 | HAMP | c.224G>A (p.Arg75Gln) n.2495G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35285011G>C | CA405301651 | HAMP | c.224G>C (p.Arg75Pro) n.2495G>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35285011G= | CA2333586135 | HAMP | c.224G= (p.Arg75=) n.2495G= | |
19 | g.35285011G>T | CA405301654 | HAMP | c.224G>T (p.Arg75Leu) n.2495G>T | |
19 | g.35285012A= | CA2333586136 | HAMP | c.225A= (p.Arg75=) n.2496A= | |
19 | g.35285012A>C | CA507041717 | HAMP | c.225A>C (p.Arg75=) n.2496A>C | |
19 | g.35285012A>G | CA507041723 | HAMP | c.225A>G (p.Arg75=) n.2496A>G | |
19 | g.35285012A>T | CA507041720 | HAMP | c.225A>T (p.Arg75=) n.2496A>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35285013T>A | CA405301659 | HAMP | c.226T>A (p.Ser76Thr) n.2497T>A | gnomAD v4 |
19 | g.35285013T>C | CA405301661 | HAMP | c.226T>C (p.Ser76Pro) n.2497T>C | |
19 | g.35285013T>G | CA405301665 | HAMP | c.226T>G (p.Ser76Ala) n.2497T>G | |
19 | g.35285014C>A | CA405301675 | HAMP | c.227C>A (p.Ser76Ter) n.2498C>A | gnomAD v4 |
19 | g.35285014C>G | CA405301672 | HAMP | c.227C>G (p.Ser76Ter) n.2498C>G | |
19 | g.35285014C>T | CA405301669 | HAMP | c.227C>T (p.Ser76Leu) n.2498C>T | |
19 | g.35285015A= | CA2333586137 | HAMP | c.228A= (p.Ser76=) n.2499A= | |
19 | g.35285015A>C | CA507041738 | HAMP | c.228A>C (p.Ser76=) n.2499A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.35285015A>G | CA507041739 | HAMP | c.228A>G (p.Ser76=) n.2499A>G | |
19 | g.35285015A>T | CA507041740 | HAMP | c.228A>T (p.Ser76=) n.2499A>T | |
19 | g.35285016A>C | CA405301678 | HAMP | c.229A>C (p.Lys77Gln) n.2500A>C | |
19 | g.35285016A>G | CA405301682 | HAMP | c.229A>G (p.Lys77Glu) n.2500A>G | |
19 | g.35285016A>T | CA405301684 | HAMP | c.229A>T (p.Lys77Ter) n.2500A>T | |
19 | g.35285017A>C | CA405301685 | HAMP | c.230A>C (p.Lys77Thr) n.2501A>C | |
19 | g.35285017A>G | CA405301688 | HAMP | c.230A>G (p.Lys77Arg) n.2501A>G | |
19 | g.35285017A>T | CA405301691 | HAMP | c.230A>T (p.Lys77Met) n.2501A>T | |
19 | g.35285018G>A | CA507041750 | HAMP | c.231G>A (p.Lys77=) n.2502G>A | dbSNP |
19 | g.35285018G>C | CA405301693 | HAMP | c.231G>C (p.Lys77Asn) n.2502G>C | |
19 | g.35285018G= | CA2333586138 | HAMP | c.231G= (p.Lys77=) n.2502G= | |
19 | g.35285018G>T | CA405301695 | HAMP | c.231G>T (p.Lys77Asn) n.2502G>T | |
19 | g.35285019T>A | CA405301698 | HAMP | c.232T>A (p.Cys78Ser) n.2503T>A | |
19 | g.35285019T>C | CA405301701 | HAMP | c.232T>C (p.Cys78Arg) n.2503T>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35285019T>G | CA405301704 | HAMP | c.232T>G (p.Cys78Gly) n.2503T>G | |
19 | g.35285019T= | CA2333586139 | HAMP | c.232T= (p.Cys78=) n.2503T= | |
19 | g.35285020G>A | CA405301716 | HAMP | c.233G>A (p.Cys78Tyr) n.2504G>A | dbSNP gnomAD v4 |
19 | g.35285020G>C | CA405301717 | HAMP | c.233G>C (p.Cys78Ser) n.2504G>C | |
19 | g.35285020G= | CA2333586140 | HAMP | c.233G= (p.Cys78=) n.2504G= | |
19 | g.35285020G>T | CA405301709 | HAMP | c.233G>T (p.Cys78Phe) n.2504G>T | |
19 | g.35285021T>A | CA405301719 | HAMP | c.234T>A (p.Cys78Ter) n.2505T>A | |
19 | g.35285021T>C | CA507041771 | HAMP | c.234T>C (p.Cys78=) n.2505T>C | |
19 | g.35285021T>G | CA405301720 | HAMP | c.234T>G (p.Cys78Trp) n.2505T>G |