Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.80108510A>C | CA401364945 | GAA | c.1097A>C (p.Tyr366Ser) | ClinVar dbSNP |
17 | g.80108510A>G | CA401364946 | GAA | c.1097A>G (p.Tyr366Cys) | gnomAD v4 |
17 | g.80108510A>T | CA401364947 | GAA | c.1097A>T (p.Tyr366Phe) | COSMIC |
17 | g.80108511C>A | CA401364948 | GAA | c.1098C>A (p.Tyr366Ter) | |
17 | g.80108511C>G | CA401364949 | GAA | c.1098C>G (p.Tyr366Ter) | |
17 | g.80108511C>T | CA502402382 | GAA | c.1098C>T (p.Tyr366=) | ClinVar dbSNP gnomAD v4 |
17 | g.80108511_80108512delinsCT | CA2277812792 | GAA | c.1098_1099delinsCT (p.Tyr366=) | |
17 | g.80108512del | CA16041888 | GAA | c.1099del (p.Trp367GlyfsTer25) | ClinVar dbSNP |
17 | g.80108512T>A | CA401364950 | GAA | c.1099T>A (p.Trp367Arg) | |
17 | g.80108512T>C | CA401364951 | GAA | c.1099T>C (p.Trp367Arg) | ClinVar dbSNP gnomAD v4 |
17 | g.80108512T>G | CA401364952 | GAA | c.1099T>G (p.Trp367Gly) | |
17 | g.80108512T= | CA2277812793 | GAA | c.1099T= (p.Trp367=) | |
17 | g.80108513G>A | CA401364953 | GAA | c.1100G>A (p.Trp367Ter) | ClinVar dbSNP gnomAD v2 |
17 | g.80108513G>C | CA401364954 | GAA | c.1100G>C (p.Trp367Ser) | |
17 | g.80108513G= | CA2277812794 | GAA | c.1100G= (p.Trp367=) | |
17 | g.80108513G>T | CA401364955 | GAA | c.1100G>T (p.Trp367Leu) | |
17 | g.80108514G>A | CA401364958 | GAA | c.1101G>A (p.Trp367Ter) | |
17 | g.80108514G>C | CA401364957 | GAA | c.1101G>C (p.Trp367Cys) | |
17 | g.80108514G>T | CA401364956 | GAA | c.1101G>T (p.Trp367Cys) | |
17 | g.80108515G>A | CA8815170 | GAA | c.1102G>A (p.Gly368Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.80108515G>C | CA401364959 | GAA | c.1102G>C (p.Gly368Arg) | |
17 | g.80108515G= | CA2277812795 | GAA | c.1102G= (p.Gly368=) | |
17 | g.80108515G>T | CA294892167 | GAA | c.1102G>T (p.Gly368Cys) | dbSNP |
17 | g.80108516G>A | CA294892175 | GAA | c.1103G>A (p.Gly368Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.80108516G>C | CA401364960 | GAA | c.1103G>C (p.Gly368Ala) | |
17 | g.80108516G= | CA2277812796 | GAA | c.1103G= (p.Gly368=) | |
17 | g.80108516G>T | CA8815171 | GAA | c.1103G>T (p.Gly368Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.80108517C>A | CA502402383 | GAA | c.1104C>A (p.Gly368=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.80108517C= | CA2277812797 | GAA | c.1104C= (p.Gly368=) | |
17 | g.80108517C>G | CA502402384 | GAA | c.1104C>G (p.Gly368=) | |
17 | g.80108517C>T | CA502402385 | GAA | c.1104C>T (p.Gly368=) | gnomAD v4 |
17 | g.80108518dup | CA2580095322 | GAA | c.1105dup (p.Leu369ProfsTer?) | ClinVar |
17 | g.80108518C>A | CA401364961 | GAA | c.1105C>A (p.Leu369Met) | |
17 | g.80108518C>G | CA401364962 | GAA | c.1105C>G (p.Leu369Val) | gnomAD v4 |
17 | g.80108518C>T | CA502402386 | GAA | c.1105C>T (p.Leu369=) | ClinVar dbSNP gnomAD v4 |
17 | g.80108519T>A | CA401364963 | GAA | c.1106T>A (p.Leu369Gln) | ClinVar |
17 | g.80108519T>C | CA401364964 | GAA | c.1106T>C (p.Leu369Pro) | ClinVar dbSNP gnomAD v4 |
17 | g.80108519T>G | CA401364965 | GAA | c.1106T>G (p.Leu369Arg) | |
17 | g.80108519T= | CA2277812798 | GAA | c.1106T= (p.Leu369=) | |
17 | g.80108520G>A | CA502402387 | GAA | c.1107G>A (p.Leu369=) | ClinVar |
17 | g.80108520G>C | CA502402388 | GAA | c.1107G>C (p.Leu369=) | ClinVar |
17 | g.80108520G= | CA2277812799 | GAA | c.1107G= (p.Leu369=) | |
17 | g.80108520G>T | CA8815172 | GAA | c.1107G>T (p.Leu369=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.80108521G>A | CA401364966 | GAA | c.1108G>A (p.Gly370Ser) | |
17 | g.80108521G>C | CA401364968 | GAA | c.1108G>C (p.Gly370Arg) | |
17 | g.80108521G>T | CA401364967 | GAA | c.1108G>T (p.Gly370Cys) | |
17 | g.80108522G>A | CA401364969 | GAA | c.1109G>A (p.Gly370Asp) | ClinVar dbSNP |
17 | g.80108522G>C | CA401364971 | GAA | c.1109G>C (p.Gly370Ala) | |
17 | g.80108522G= | CA2277812800 | GAA | c.1109G= (p.Gly370=) | |
17 | g.80108522G>T | CA401364970 | GAA | c.1109G>T (p.Gly370Val) |