Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.240878035C>A | CA351319479 | AGXT | c.956C>A (p.Pro319His) n.734C>A | |
2 | g.240878035C= | CA1339335755 | AGXT | c.956C= (p.Pro319=) n.734C= | |
2 | g.240878035C>G | CA351319480 | AGXT | c.956C>G (p.Pro319Arg) n.734C>G | |
2 | g.240878035C>T | CA275767 | AGXT | c.956C>T (p.Pro319Leu) n.734C>T | ClinVar dbSNP |
2 | g.240878035_240878037delinsCCA | CA1339335756 | AGXT | c.956_958delinsCCA (p.Pro319=) n.734_736delinsCCA | |
2 | g.240878036C>A | CA432026133 | AGXT | c.957C>A (p.Pro319=) n.735C>A | gnomAD v4 |
2 | g.240878036C= | CA1339335757 | AGXT | c.957C= (p.Pro319=) n.735C= | |
2 | g.240878036C>G | CA432026129 | AGXT | c.957C>G (p.Pro319=) n.735C>G | |
2 | g.240878036C>T | CA432026131 | AGXT | c.957C>T (p.Pro319=) n.735C>T | ClinVar dbSNP gnomAD v4 |
2 | g.240878038_240878039del | CA275861 | AGXT | c.959_960del (p.Thr320SerfsTer11) n.737_738del | dbSNP gnomAD v4 |
2 | g.240878037A= | CA1339335758 | AGXT | c.958A= (p.Thr320=) n.736A= | |
2 | g.240878037A>C | CA68180825 | AGXT | c.958A>C (p.Thr320Pro) n.736A>C | dbSNP |
2 | g.240878037A>G | CA351319481 | AGXT | c.958A>G (p.Thr320Ala) n.736A>G | |
2 | g.240878037A>T | CA351319482 | AGXT | c.958A>T (p.Thr320Ser) n.736A>T | |
2 | g.240878038C>A | CA351319483 | AGXT | c.959C>A (p.Thr320Lys) n.737C>A | |
2 | g.240878038C>G | CA351319484 | AGXT | c.959C>G (p.Thr320Arg) n.737C>G | |
2 | g.240878038C>T | CA351319485 | AGXT | c.959C>T (p.Thr320Ile) n.737C>T | COSMIC |
2 | g.240878039del | CA2739279278 | AGXT | c.960del (p.Val321SerfsTer20) n.738del | |
2 | g.240878039A= | CA1339335759 | AGXT | c.960A= (p.Thr320=) n.738A= | |
2 | g.240878039A>C | CA432026145 | AGXT | c.960A>C (p.Thr320=) n.738A>C | |
2 | g.240878039A>G | CA432026147 | AGXT | c.960A>G (p.Thr320=) n.738A>G | dbSNP |
2 | g.240878039A>T | CA432026149 | AGXT | c.960A>T (p.Thr320=) n.738A>T | |
2 | g.240878040G>A | CA351319488 | AGXT | c.961G>A (p.Val321Ile) n.739G>A | |
2 | g.240878040G>C | CA351319487 | AGXT | c.961G>C (p.Val321Leu) n.739G>C | |
2 | g.240878040G>T | CA351319486 | AGXT | c.961G>T (p.Val321Phe) n.739G>T | ClinVar dbSNP |
2 | g.240878041T>A | CA351319489 | AGXT | c.962T>A (p.Val321Asp) n.740T>A | |
2 | g.240878041T>C | CA351319490 | AGXT | c.962T>C (p.Val321Ala) n.740T>C | |
2 | g.240878041T>G | CA351319491 | AGXT | c.962T>G (p.Val321Gly) n.740T>G | |
2 | g.240878042C>A | CA432026158 | AGXT | c.963C>A (p.Val321=) n.741C>A | |
2 | g.240878042C>G | CA432026161 | AGXT | c.963C>G (p.Val321=) n.741C>G | |
2 | g.240878042C>T | CA432026162 | AGXT | c.963C>T (p.Val321=) n.741C>T | gnomAD v4 |
2 | g.240878043A= | CA1339335760 | AGXT | c.964A= (p.Thr322=) n.742A= | |
2 | g.240878043A>C | CA351319492 | AGXT | c.964A>C (p.Thr322Pro) n.742A>C | dbSNP |
2 | g.240878043A>G | CA351319493 | AGXT | c.964A>G (p.Thr322Ala) n.742A>G | |
2 | g.240878043A>T | CA351319494 | AGXT | c.964A>T (p.Thr322Ser) n.742A>T | |
2 | g.240878044C>A | CA351319495 | AGXT | c.965C>A (p.Thr322Asn) n.743C>A | |
2 | g.240878044C>G | CA351319496 | AGXT | c.965C>G (p.Thr322Ser) n.743C>G | gnomAD v4 |
2 | g.240878044C>T | CA351319497 | AGXT | c.965C>T (p.Thr322Ile) n.743C>T | gnomAD v4 |
2 | g.240878045C>A | CA432026170 | AGXT | c.966C>A (p.Thr322=) n.744C>A | |
2 | g.240878045C>G | CA432026172 | AGXT | c.966C>G (p.Thr322=) n.744C>G | |
2 | g.240878045C>T | CA432026173 | AGXT | c.966C>T (p.Thr322=) n.744C>T | dbSNP |
2 | g.240878046A>C | CA351319498 | AGXT | c.967A>C (p.Thr323Pro) n.745A>C | |
2 | g.240878046A>G | CA351319499 | AGXT | c.967A>G (p.Thr323Ala) n.745A>G | |
2 | g.240878046A>T | CA351319500 | AGXT | c.967A>T (p.Thr323Ser) n.745A>T | |
2 | g.240878047C>A | CA351319502 | AGXT | c.968C>A (p.Thr323Asn) n.746C>A | |
2 | g.240878047C>G | CA351319503 | AGXT | c.968C>G (p.Thr323Ser) n.746C>G | |
2 | g.240878047C>T | CA351319501 | AGXT | c.968C>T (p.Thr323Ile) n.746C>T | gnomAD v4 |
2 | g.240878047_240878049delinsCTG | CA1339335761 | AGXT | c.968_970delinsCTG (p.Thr323=) n.746_748delinsCTG | |
2 | g.240878048T>A | CA432026185 | AGXT | c.969T>A (p.Thr323=) n.747T>A | |
2 | g.240878048T>C | CA432026186 | AGXT | c.969T>C (p.Thr323=) n.747T>C |