Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.35284803A= | CA2333586013 | HAMP | c.105A= (p.Ala35=) n.2287A= | |
19 | g.35284803A>C | CA507040972 | HAMP | c.105A>C (p.Ala35=) n.2287A>C | |
19 | g.35284803A>G | CA507040977 | HAMP | c.105A>G (p.Ala35=) n.2287A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284803A>T | CA507040974 | HAMP | c.105A>T (p.Ala35=) n.2287A>T | |
19 | g.35284804G>A | CA9375792 | HAMP | c.106G>A (p.Glu36Lys) n.2288G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35284804G>C | CA405300549 | HAMP | c.106G>C (p.Glu36Gln) n.2288G>C | |
19 | g.35284804G= | CA2333586014 | HAMP | c.106G= (p.Glu36=) n.2288G= | |
19 | g.35284804G>T | CA405300552 | HAMP | c.106G>T (p.Glu36Ter) n.2288G>T | |
19 | g.35284805A= | CA2333586015 | HAMP | c.107A= (p.Glu36=) n.2289A= | |
19 | g.35284805A>C | CA405300556 | HAMP | c.107A>C (p.Glu36Ala) n.2289A>C | dbSNP gnomAD v2 |
19 | g.35284805A>G | CA405300562 | HAMP | c.107A>G (p.Glu36Gly) n.2289A>G | |
19 | g.35284805A>T | CA405300563 | HAMP | c.107A>T (p.Glu36Val) n.2289A>T | |
19 | g.35284806G>A | CA507040991 | HAMP | c.108G>A (p.Glu36=) n.2290G>A | ClinVar dbSNP gnomAD v4 |
19 | g.35284806G>C | CA405300567 | HAMP | c.108G>C (p.Glu36Asp) n.2290G>C | |
19 | g.35284806G= | CA2333586016 | HAMP | c.108G= (p.Glu36=) n.2290G= | |
19 | g.35284806G>T | CA405300570 | HAMP | c.108G>T (p.Glu36Asp) n.2290G>T | |
19 | g.35284807C>A | CA405300579 | HAMP | c.109C>A (p.Leu37Met) n.2291C>A | |
19 | g.35284807C= | CA2333586017 | HAMP | c.109C= (p.Leu37=) n.2291C= | |
19 | g.35284807C>G | CA405300581 | HAMP | c.109C>G (p.Leu37Val) n.2291C>G | |
19 | g.35284807C>T | CA507041010 | HAMP | c.109C>T (p.Leu37=) n.2291C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284808T>A | CA405300586 | HAMP | c.110T>A (p.Leu37Gln) n.2292T>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284808T>C | CA405300584 | HAMP | c.110T>C (p.Leu37Pro) n.2292T>C | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284808T>G | CA405300585 | HAMP | c.110T>G (p.Leu37Arg) n.2292T>G | |
19 | g.35284808T= | CA2333586018 | HAMP | c.110T= (p.Leu37=) n.2292T= | |
19 | g.35284809G>A | CA507041026 | HAMP | c.111G>A (p.Leu37=) n.2293G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284809G>C | CA507041029 | HAMP | c.111G>C (p.Leu37=) n.2293G>C | |
19 | g.35284809G= | CA2333586019 | HAMP | c.111G= (p.Leu37=) n.2293G= | |
19 | g.35284809G>T | CA507041032 | HAMP | c.111G>T (p.Leu37=) n.2293G>T | |
19 | g.35284810C>A | CA405300587 | HAMP | c.112C>A (p.Gln38Lys) n.2294C>A | |
19 | g.35284810C>G | CA405300588 | HAMP | c.112C>G (p.Gln38Glu) n.2294C>G | |
19 | g.35284810C>T | CA405300590 | HAMP | c.112C>T (p.Gln38Ter) n.2294C>T | |
19 | g.35284811A>C | CA405300593 | HAMP | c.113A>C (p.Gln38Pro) n.2295A>C | |
19 | g.35284811A>G | CA405300598 | HAMP | c.113A>G (p.Gln38Arg) n.2295A>G | |
19 | g.35284811A>T | CA405300601 | HAMP | c.113A>T (p.Gln38Leu) n.2295A>T | |
19 | g.35284812del | CA2695228583 | HAMP | c.114del (p.Gln38HisfsTer?) n.2296del | |
19 | g.35284812A= | CA2333586020 | HAMP | c.114A= (p.Gln38=) n.2296A= | |
19 | g.35284812A>C | CA405300606 | HAMP | c.114A>C (p.Gln38His) n.2296A>C | |
19 | g.35284812A>G | CA507041061 | HAMP | c.114A>G (p.Gln38=) n.2296A>G | ClinVar dbSNP |
19 | g.35284812A>T | CA405300610 | HAMP | c.114A>T (p.Gln38His) n.2296A>T | |
19 | g.35284813C>A | CA405300614 | HAMP | c.115C>A (p.Pro39Thr) n.2297C>A | |
19 | g.35284813C= | CA2333586021 | HAMP | c.115C= (p.Pro39=) n.2297C= | |
19 | g.35284813C>G | CA405300617 | HAMP | c.115C>G (p.Pro39Ala) n.2297C>G | |
19 | g.35284813C>T | CA9375793 | HAMP | c.115C>T (p.Pro39Ser) n.2297C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35284814C>A | CA405300626 | HAMP | c.116C>A (p.Pro39His) n.2298C>A | gnomAD v4 |
19 | g.35284814C>G | CA405300628 | HAMP | c.116C>G (p.Pro39Arg) n.2298C>G | |
19 | g.35284814C>T | CA405300624 | HAMP | c.116C>T (p.Pro39Leu) n.2298C>T | gnomAD v4 |
19 | g.35284815C>A | CA507041078 | HAMP | c.117C>A (p.Pro39=) n.2299C>A | |
19 | g.35284815C= | CA2333586022 | HAMP | c.117C= (p.Pro39=) n.2299C= | |
19 | g.35284815C>G | CA507041081 | HAMP | c.117C>G (p.Pro39=) n.2299C>G | |
19 | g.35284815C>T | CA9375794 | HAMP | c.117C>T (p.Pro39=) n.2299C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |