Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.80107816A= | CA2277812404 | GAA | c.875A= (p.Tyr292=) | |
17 | g.80107816A>C | CA401363867 | GAA | c.875A>C (p.Tyr292Ser) | |
17 | g.80107816A>G | CA16041886 | GAA | c.875A>G (p.Tyr292Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.80107816A>T | CA401363865 | GAA | c.875A>T (p.Tyr292Phe) | |
17 | g.80107817C>A | CA401363869 | GAA | c.876C>A (p.Tyr292Ter) | |
17 | g.80107817C= | CA2277812405 | GAA | c.876C= (p.Tyr292=) | |
17 | g.80107817C>G | CA401363871 | GAA | c.876C>G (p.Tyr292Ter) | ClinVar dbSNP |
17 | g.80107817C>T | CA8815080 | GAA | c.876C>T (p.Tyr292=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.80107818G>A | CA116622 | GAA | c.877G>A (p.Gly293Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.80107818G>C | CA401363876 | GAA | c.877G>C (p.Gly293Arg) | ClinVar dbSNP |
17 | g.80107818G= | CA2277812406 | GAA | c.877G= (p.Gly293=) | |
17 | g.80107818G>T | CA401363875 | GAA | c.877G>T (p.Gly293Trp) | gnomAD v4 |
17 | g.80107819G>A | CA401363879 | GAA | c.878G>A (p.Gly293Glu) | |
17 | g.80107819G>C | CA401363881 | GAA | c.878G>C (p.Gly293Ala) | |
17 | g.80107819G= | CA2277812407 | GAA | c.878G= (p.Gly293=) | |
17 | g.80107819G>T | CA401363883 | GAA | c.878G>T (p.Gly293Val) | dbSNP |
17 | g.80107820G>A | CA502402736 | GAA | c.879G>A (p.Gly293=) | ClinVar dbSNP gnomAD v4 |
17 | g.80107820G>C | CA502402737 | GAA | c.879G>C (p.Gly293=) | |
17 | g.80107820G>T | CA502402738 | GAA | c.879G>T (p.Gly293=) | |
17 | g.80107821T>A | CA401363885 | GAA | c.880T>A (p.Ser294Thr) | |
17 | g.80107821T>C | CA401363887 | GAA | c.880T>C (p.Ser294Pro) | |
17 | g.80107821T>G | CA401363889 | GAA | c.880T>G (p.Ser294Ala) | |
17 | g.80107822C>A | CA401363891 | GAA | c.881C>A (p.Ser294Tyr) | |
17 | g.80107822C>G | CA401363894 | GAA | c.881C>G (p.Ser294Cys) | |
17 | g.80107822C>T | CA401363892 | GAA | c.881C>T (p.Ser294Phe) | |
17 | g.80107823T>A | CA502402739 | GAA | c.882T>A (p.Ser294=) | |
17 | g.80107823T>C | CA502402740 | GAA | c.882T>C (p.Ser294=) | |
17 | g.80107823T>G | CA502402741 | GAA | c.882T>G (p.Ser294=) | |
17 | g.80107824C>A | CA8815081 | GAA | c.883C>A (p.His295Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.80107824C= | CA2277812408 | GAA | c.883C= (p.His295=) | |
17 | g.80107824C>G | CA401363897 | GAA | c.883C>G (p.His295Asp) | |
17 | g.80107824C>T | CA401363899 | GAA | c.883C>T (p.His295Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.80107825A>C | CA401363901 | GAA | c.884A>C (p.His295Pro) | |
17 | g.80107825A>G | CA401363903 | GAA | c.884A>G (p.His295Arg) | |
17 | g.80107825A>T | CA401363905 | GAA | c.884A>T (p.His295Leu) | |
17 | g.80107826C>A | CA401363907 | GAA | c.885C>A (p.His295Gln) | |
17 | g.80107826C>G | CA401363908 | GAA | c.885C>G (p.His295Gln) | |
17 | g.80107826C>T | CA502402742 | GAA | c.885C>T (p.His295=) | |
17 | g.80107827C>A | CA401363910 | GAA | c.886C>A (p.Pro296Thr) | |
17 | g.80107827C>G | CA401363912 | GAA | c.886C>G (p.Pro296Ala) | gnomAD v4 |
17 | g.80107827C>T | CA401363914 | GAA | c.886C>T (p.Pro296Ser) | |
17 | g.80107828C>A | CA401363920 | GAA | c.887C>A (p.Pro296His) | |
17 | g.80107828C>G | CA401363918 | GAA | c.887C>G (p.Pro296Arg) | |
17 | g.80107828C>T | CA401363916 | GAA | c.887C>T (p.Pro296Leu) | |
17 | g.80107829T>A | CA502402743 | GAA | c.888T>A (p.Pro296=) | gnomAD v4 |
17 | g.80107829T>C | CA502402744 | GAA | c.888T>C (p.Pro296=) | |
17 | g.80107829T>G | CA502402745 | GAA | c.888T>G (p.Pro296=) | |
17 | g.80107830T>A | CA401363922 | GAA | c.889T>A (p.Phe297Ile) | |
17 | g.80107830T>C | CA401363924 | GAA | c.889T>C (p.Phe297Leu) | |
17 | g.80107830T>G | CA401363926 | GAA | c.889T>G (p.Phe297Val) |