Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.230710736G>A | CA345207711 | AGT | c.88C>T (p.His30Tyr) n.599C>T c.115C>T (p.His39Tyr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.230710736G>C | CA345207712 | AGT | c.88C>G (p.His30Asp) n.599C>G c.115C>G (p.His39Asp) | |
1 | g.230710736G= | CA1226658845 | AGT | c.88C= (p.His30=) n.599C= c.115C= (p.His39=) | |
1 | g.230710736G>T | CA345207714 | AGT | c.88C>A (p.His30Asn) n.599C>A c.115C>A (p.His39Asn) | |
1 | g.230710737T>A | CA424037003 | AGT | c.87A>T (p.Ile29=) n.598A>T c.114A>T (p.Ile38=) | |
1 | g.230710737T>C | CA345207716 | AGT | c.87A>G (p.Ile29Met) n.598A>G c.114A>G (p.Ile38Met) | |
1 | g.230710737T>G | CA424037004 | AGT | c.87A>C (p.Ile29=) n.598A>C c.114A>C (p.Ile38=) | gnomAD v4 |
1 | g.230710738A>C | CA345207718 | AGT | c.86T>G (p.Ile29Arg) n.597T>G c.113T>G (p.Ile38Arg) | |
1 | g.230710738A>G | CA345207720 | AGT | c.86T>C (p.Ile29Thr) n.597T>C c.113T>C (p.Ile38Thr) | |
1 | g.230710738A>T | CA345207722 | AGT | c.86T>A (p.Ile29Lys) n.597T>A c.113T>A (p.Ile38Lys) | COSMIC |
1 | g.230710739T>A | CA345207723 | AGT | c.85A>T (p.Ile29Leu) n.596A>T c.112A>T (p.Ile38Leu) | |
1 | g.230710739T>C | CA345207725 | AGT | c.85A>G (p.Ile29Val) n.596A>G c.112A>G (p.Ile38Val) | gnomAD v4 |
1 | g.230710739T>G | CA38872450 | AGT | c.85A>C (p.Ile29Leu) n.596A>C c.112A>C (p.Ile38Leu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.230710739T= | CA1226658851 | AGT | c.85A= (p.Ile29=) n.596A= c.112A= (p.Ile38=) | |
1 | g.230710739_230710740delinsTG | CA1226658850 | AGT | c.84_85delinsCA (p.Tyr28=) n.595_596delinsCA c.111_112delinsCA (p.Tyr37=) | |
1 | g.230710740del | CA1013240076 | AGT | c.84del (p.Tyr28Ter) n.595del c.111del (p.Tyr37Ter) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.230710740G>A | CA424037010 | AGT | c.84C>T (p.Tyr28=) n.595C>T c.111C>T (p.Tyr37=) | gnomAD v4 COSMIC |
1 | g.230710740G>C | CA345207727 | AGT | c.84C>G (p.Tyr28Ter) n.595C>G c.111C>G (p.Tyr37Ter) | |
1 | g.230710740G>T | CA345207728 | AGT | c.84C>A (p.Tyr28Ter) n.595C>A c.111C>A (p.Tyr37Ter) | |
1 | g.230710741T>A | CA345207733 | AGT | c.83A>T (p.Tyr28Phe) n.594A>T c.110A>T (p.Tyr37Phe) | |
1 | g.230710741T>C | CA345207734 | AGT | c.83A>G (p.Tyr28Cys) n.594A>G c.110A>G (p.Tyr37Cys) | |
1 | g.230710741T>G | CA345207731 | AGT | c.83A>C (p.Tyr28Ser) n.594A>C c.110A>C (p.Tyr37Ser) | |
1 | g.230710742A>C | CA345207736 | AGT | c.82T>G (p.Tyr28Asp) n.593T>G c.109T>G (p.Tyr37Asp) | |
1 | g.230710742A>G | CA345207738 | AGT | c.82T>C (p.Tyr28His) n.593T>C c.109T>C (p.Tyr37His) | |
1 | g.230710742A>T | CA345207740 | AGT | c.82T>A (p.Tyr28Asn) n.593T>A c.109T>A (p.Tyr37Asn) | gnomAD v4 |
1 | g.230710743C>A | CA424037016 | AGT | c.81G>T (p.Val27=) n.592G>T c.108G>T (p.Val36=) | |
1 | g.230710743C>G | CA424037018 | AGT | c.81G>C (p.Val27=) n.592G>C c.108G>C (p.Val36=) | |
1 | g.230710743C>T | CA424037019 | AGT | c.81G>A (p.Val27=) n.592G>A c.108G>A (p.Val36=) | |
1 | g.230710744A= | CA1226658858 | AGT | c.80T= (p.Val27=) n.591T= c.107T= (p.Val36=) | |
1 | g.230710744A>C | CA345207741 | AGT | c.80T>G (p.Val27Gly) n.591T>G c.107T>G (p.Val36Gly) | dbSNP |
1 | g.230710744A>G | CA345207742 | AGT | c.80T>C (p.Val27Ala) n.591T>C c.107T>C (p.Val36Ala) | |
1 | g.230710744A>T | CA345207744 | AGT | c.80T>A (p.Val27Glu) n.591T>A c.107T>A (p.Val36Glu) | |
1 | g.230710745C>A | CA345207746 | AGT | c.79G>T (p.Val27Leu) n.590G>T c.106G>T (p.Val36Leu) | |
1 | g.230710745C= | CA1226658859 | AGT | c.79G= (p.Val27=) n.590G= c.106G= (p.Val36=) | |
1 | g.230710745C>G | CA345207749 | AGT | c.79G>C (p.Val27Leu) n.590G>C c.106G>C (p.Val36Leu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.230710745C>T | CA345207748 | AGT | c.79G>A (p.Val27Met) n.590G>A c.106G>A (p.Val36Met) | |
1 | g.230710746C>A | CA424037026 | AGT | c.78G>T (p.Arg26=) n.589G>T c.105G>T (p.Arg35=) | |
1 | g.230710746C>G | CA424037027 | AGT | c.78G>C (p.Arg26=) n.589G>C c.105G>C (p.Arg35=) | |
1 | g.230710746C>T | CA424037029 | AGT | c.78G>A (p.Arg26=) n.589G>A c.105G>A (p.Arg35=) | |
1 | g.230710747C>A | CA345207752 | AGT | c.77G>T (p.Arg26Leu) n.588G>T c.104G>T (p.Arg35Leu) | |
1 | g.230710747C= | CA1226658864 | AGT | c.77G= (p.Arg26=) n.588G= c.104G= (p.Arg35=) | |
1 | g.230710747C>G | CA345207754 | AGT | c.77G>C (p.Arg26Pro) n.588G>C c.104G>C (p.Arg35Pro) | |
1 | g.230710747C>T | CA1448386 | AGT | c.77G>A (p.Arg26Gln) n.588G>A c.104G>A (p.Arg35Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.230710748G>A | CA1448387 | AGT | c.76C>T (p.Arg26Trp) n.587C>T c.103C>T (p.Arg35Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.230710748G>C | CA345207757 | AGT | c.76C>G (p.Arg26Gly) n.587C>G c.103C>G (p.Arg35Gly) | |
1 | g.230710748G= | CA1226658871 | AGT | c.76C= (p.Arg26=) n.587C= c.103C= (p.Arg35=) | |
1 | g.230710748G>T | CA424037032 | AGT | c.76C>A (p.Arg26=) n.587C>A c.103C>A (p.Arg35=) | |
1 | g.230710749G>A | CA424037035 | AGT | c.75C>T (p.Asp25=) n.586C>T c.102C>T (p.Asp34=) | gnomAD v4 |
1 | g.230710749G>C | CA345207760 | AGT | c.75C>G (p.Asp25Glu) n.586C>G c.102C>G (p.Asp34Glu) | |
1 | g.230710749G>T | CA345207759 | AGT | c.75C>A (p.Asp25Glu) n.586C>A c.102C>A (p.Asp34Glu) |