Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.240874001T>A | CA351316834 | AGXT | c.619T>A (p.Ser207Thr) n.332+952T>A | |
2 | g.240874001T>C | CA351316839 | AGXT | c.619T>C (p.Ser207Pro) n.332+952T>C | |
2 | g.240874001T>G | CA351316837 | AGXT | c.619T>G (p.Ser207Ala) n.332+952T>G | |
2 | g.240874002C>A | CA351316841 | AGXT | c.620C>A (p.Ser207Tyr) n.332+953C>A | |
2 | g.240874002C>G | CA351316843 | AGXT | c.620C>G (p.Ser207Cys) n.332+953C>G | |
2 | g.240874002C>T | CA351316845 | AGXT | c.620C>T (p.Ser207Phe) n.332+953C>T | |
2 | g.240874003C>A | CA432024133 | AGXT | c.621C>A (p.Ser207=) n.332+954C>A | |
2 | g.240874003C>G | CA432024134 | AGXT | c.621C>G (p.Ser207=) n.332+954C>G | |
2 | g.240874003C>T | CA432024136 | AGXT | c.621C>T (p.Ser207=) n.332+954C>T | |
2 | g.240874004C>A | CA2209174 | AGXT | c.622C>A (p.Gln208Lys) n.332+955C>A | dbSNP ExAC gnomAD v2 |
2 | g.240874004C= | CA1339333568 | AGXT | c.622C= (p.Gln208=) n.332+955C= | |
2 | g.240874004C>G | CA351316848 | AGXT | c.622C>G (p.Gln208Glu) n.332+955C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874004C>T | CA351316850 | AGXT | c.622C>T (p.Gln208Ter) n.332+955C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874005A= | CA1339333569 | AGXT | c.623A= (p.Gln208=) n.332+956A= | |
2 | g.240874005A>C | CA351316852 | AGXT | c.623A>C (p.Gln208Pro) n.332+956A>C | |
2 | g.240874005A>G | CA2209175 | AGXT | c.623A>G (p.Gln208Arg) n.332+956A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240874005A>T | CA351316854 | AGXT | c.623A>T (p.Gln208Leu) n.332+956A>T | |
2 | g.240874006G>A | CA432024140 | AGXT | c.624G>A (p.Gln208=) n.332+957G>A | ClinVar dbSNP |
2 | g.240874006G>C | CA351316856 | AGXT | c.624G>C (p.Gln208His) n.332+957G>C | COSMIC |
2 | g.240874006G>T | CA351316858 | AGXT | c.624G>T (p.Gln208His) n.332+957G>T | |
2 | g.240874007A>C | CA351316861 | AGXT | c.625A>C (p.Lys209Gln) n.332+958A>C | |
2 | g.240874007A>G | CA351316865 | AGXT | c.625A>G (p.Lys209Glu) n.332+958A>G | gnomAD v4 COSMIC |
2 | g.240874007A>T | CA351316862 | AGXT | c.625A>T (p.Lys209Ter) n.332+958A>T | |
2 | g.240874008del | CA2697550616 | AGXT | c.626del (p.Lys209ArgfsTer3) n.332+959del | ClinVar |
2 | g.240874008A>C | CA351316867 | AGXT | c.626A>C (p.Lys209Thr) n.332+959A>C | gnomAD v4 |
2 | g.240874008A>G | CA351316869 | AGXT | c.626A>G (p.Lys209Arg) n.332+959A>G | COSMIC |
2 | g.240874008A>T | CA351316871 | AGXT | c.626A>T (p.Lys209Met) n.332+959A>T | |
2 | g.240874009G>A | CA432024144 | AGXT | c.627G>A (p.Lys209=) n.332+960G>A | ClinVar COSMIC |
2 | g.240874009G>C | CA351316873 | AGXT | c.627G>C (p.Lys209Asn) n.332+960G>C | |
2 | g.240874009G= | CA1339333570 | AGXT | c.627G= (p.Lys209=) n.332+960G= | |
2 | g.240874009G>T | CA351316875 | AGXT | c.627G>T (p.Lys209Asn) n.332+960G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.240874010G>A | CA351316878 | AGXT | c.628G>A (p.Ala210Thr) n.332+961G>A | gnomAD v4 |
2 | g.240874010G>C | CA275726 | AGXT | c.628G>C (p.Ala210Pro) n.332+961G>C | ClinVar dbSNP |
2 | g.240874010G= | CA1339333571 | AGXT | c.628G= (p.Ala210=) n.332+961G= | |
2 | g.240874010G>T | CA351316881 | AGXT | c.628G>T (p.Ala210Ser) n.332+961G>T | |
2 | g.240874011C>A | CA351316883 | AGXT | c.629C>A (p.Ala210Asp) n.332+962C>A | |
2 | g.240874011C>G | CA351316885 | AGXT | c.629C>G (p.Ala210Gly) n.332+962C>G | |
2 | g.240874011C>T | CA351316887 | AGXT | c.629C>T (p.Ala210Val) n.332+962C>T | gnomAD v4 |
2 | g.240874012C>A | CA432024154 | AGXT | c.630C>A (p.Ala210=) n.332+963C>A | |
2 | g.240874012C= | CA1339333572 | AGXT | c.630C= (p.Ala210=) n.332+963C= | |
2 | g.240874012C>G | CA432024155 | AGXT | c.630C>G (p.Ala210=) n.332+963C>G | gnomAD v4 |
2 | g.240874012C>T | CA432024156 | AGXT | c.630C>T (p.Ala210=) n.332+963C>T | ClinVar dbSNP gnomAD v4 |
2 | g.240874013C>A | CA351316889 | AGXT | c.631C>A (p.Leu211Met) n.332+964C>A | |
2 | g.240874013C>G | CA351316890 | AGXT | c.631C>G (p.Leu211Val) n.332+964C>G | |
2 | g.240874013C>T | CA432024157 | AGXT | c.631C>T (p.Leu211=) n.332+964C>T | COSMIC |
2 | g.240874014T>A | CA351316893 | AGXT | c.632T>A (p.Leu211Gln) n.332+965T>A | |
2 | g.240874014T>C | CA351316897 | AGXT | c.632T>C (p.Leu211Pro) n.332+965T>C | |
2 | g.240874014T>G | CA351316895 | AGXT | c.632T>G (p.Leu211Arg) n.332+965T>G | ClinVar |
2 | g.240874015G>A | CA432024159 | AGXT | c.633G>A (p.Leu211=) n.332+966G>A | |
2 | g.240874015G>C | CA432024160 | AGXT | c.633G>C (p.Leu211=) n.332+966G>C |