Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130873037_130878415del | CA658820873 | ABL1 | c.1142_1328del c.1085_1271del | |
9 | g.130874868_130875052del | CA645556988 | ABL1 | c.1143_1327del c.1086_1270del | COSMIC |
9 | g.130874969A= | CA1881478302 | ABL1 | c.1244A= (p.His415=) c.1187A= (p.His396=) | |
9 | g.130874969A>C | CA375249969 | ABL1 | c.1244A>C (p.His415Pro) c.1187A>C (p.His396Pro) | COSMIC |
9 | g.130874969A>G | CA16602558 | ABL1 | c.1244A>G (p.His415Arg) c.1187A>G (p.His396Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
9 | g.130874969A>T | CA375249970 | ABL1 | c.1244A>T (p.His415Leu) c.1187A>T (p.His396Leu) | |
9 | g.130874970T>A | CA375249971 | ABL1 | c.1245T>A (p.His415Gln) c.1188T>A (p.His396Gln) | |
9 | g.130874970T>C | CA467395425 | ABL1 | c.1245T>C (p.His415=) c.1188T>C (p.His396=) | dbSNP |
9 | g.130874970T>G | CA375249972 | ABL1 | c.1245T>G (p.His415Gln) c.1188T>G (p.His396Gln) | |
9 | g.130874970T= | CA1881478305 | ABL1 | c.1245T= (p.His415=) c.1188T= (p.His396=) | |
9 | g.130874971G>A | CA375249973 | ABL1 | c.1246G>A (p.Ala416Thr) c.1189G>A (p.Ala397Thr) | |
9 | g.130874971G>C | CA375249974 | ABL1 | c.1246G>C (p.Ala416Pro) c.1189G>C (p.Ala397Pro) | |
9 | g.130874971G>T | CA375249975 | ABL1 | c.1246G>T (p.Ala416Ser) c.1189G>T (p.Ala397Ser) | |
9 | g.130874972C>A | CA375249976 | ABL1 | c.1247C>A (p.Ala416Asp) c.1190C>A (p.Ala397Asp) | |
9 | g.130874972C>G | CA375249977 | ABL1 | c.1247C>G (p.Ala416Gly) c.1190C>G (p.Ala397Gly) | |
9 | g.130874972C>T | CA375249978 | ABL1 | c.1247C>T (p.Ala416Val) c.1190C>T (p.Ala397Val) | ClinVar dbSNP |
9 | g.130874973T>A | CA467395426 | ABL1 | c.1248T>A (p.Ala416=) c.1191T>A (p.Ala397=) | dbSNP |
9 | g.130874973T>C | CA5285400 | ABL1 | c.1248T>C (p.Ala416=) c.1191T>C (p.Ala397=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.130874973T>G | CA467395427 | ABL1 | c.1248T>G (p.Ala416=) c.1191T>G (p.Ala397=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.130874973T= | CA1881478308 | ABL1 | c.1248T= (p.Ala416=) c.1191T= (p.Ala397=) | |
9 | g.130874974G>A | CA375249979 | ABL1 | c.1249G>A (p.Gly417Arg) c.1192G>A (p.Gly398Arg) | |
9 | g.130874974G>C | CA375249980 | ABL1 | c.1249G>C (p.Gly417Arg) c.1192G>C (p.Gly398Arg) | |
9 | g.130874974G>T | CA375249981 | ABL1 | c.1249G>T (p.Gly417Ter) c.1192G>T (p.Gly398Ter) | |
9 | g.130874975G>A | CA375249982 | ABL1 | c.1250G>A (p.Gly417Glu) c.1193G>A (p.Gly398Glu) | dbSNP |
9 | g.130874975G>C | CA375249983 | ABL1 | c.1250G>C (p.Gly417Ala) c.1193G>C (p.Gly398Ala) | |
9 | g.130874975G= | CA1881478310 | ABL1 | c.1250G= (p.Gly417=) c.1193G= (p.Gly398=) | |
9 | g.130874975G>T | CA375249984 | ABL1 | c.1250G>T (p.Gly417Val) c.1193G>T (p.Gly398Val) | |
9 | g.130874976A= | CA1881478312 | ABL1 | c.1251A= (p.Gly417=) c.1194A= (p.Gly398=) | |
9 | g.130874976A>C | CA467395428 | ABL1 | c.1251A>C (p.Gly417=) c.1194A>C (p.Gly398=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.130874976A>G | CA467395429 | ABL1 | c.1251A>G (p.Gly417=) c.1194A>G (p.Gly398=) | |
9 | g.130874976A>T | CA467395430 | ABL1 | c.1251A>T (p.Gly417=) c.1194A>T (p.Gly398=) | |
9 | g.130874977G>A | CA375249987 | ABL1 | c.1252G>A (p.Ala418Thr) c.1195G>A (p.Ala399Thr) | dbSNP |
9 | g.130874977G>C | CA375249985 | ABL1 | c.1252G>C (p.Ala418Pro) c.1195G>C (p.Ala399Pro) | |
9 | g.130874977G>T | CA375249986 | ABL1 | c.1252G>T (p.Ala418Ser) c.1195G>T (p.Ala399Ser) | |
9 | g.130874978C>A | CA375249988 | ABL1 | c.1253C>A (p.Ala418Asp) c.1196C>A (p.Ala399Asp) | |
9 | g.130874978C>G | CA375249989 | ABL1 | c.1253C>G (p.Ala418Gly) c.1196C>G (p.Ala399Gly) | |
9 | g.130874978C>T | CA375249990 | ABL1 | c.1253C>T (p.Ala418Val) c.1196C>T (p.Ala399Val) | |
9 | g.130874979C>A | CA467395431 | ABL1 | c.1254C>A (p.Ala418=) c.1197C>A (p.Ala399=) | |
9 | g.130874979C>G | CA467395432 | ABL1 | c.1254C>G (p.Ala418=) c.1197C>G (p.Ala399=) | |
9 | g.130874979C>T | CA467395433 | ABL1 | c.1254C>T (p.Ala418=) c.1197C>T (p.Ala399=) | gnomAD v4 |
9 | g.130874980A>C | CA375249991 | ABL1 | c.1255A>C (p.Lys419Gln) c.1198A>C (p.Lys400Gln) | |
9 | g.130874980A>G | CA375249992 | ABL1 | c.1255A>G (p.Lys419Glu) c.1198A>G (p.Lys400Glu) | COSMIC |
9 | g.130874980A>T | CA375249993 | ABL1 | c.1255A>T (p.Lys419Ter) c.1198A>T (p.Lys400Ter) | |
9 | g.130874981A>C | CA375249996 | ABL1 | c.1256A>C (p.Lys419Thr) c.1199A>C (p.Lys400Thr) | |
9 | g.130874981A>G | CA375249994 | ABL1 | c.1256A>G (p.Lys419Arg) c.1199A>G (p.Lys400Arg) | |
9 | g.130874981A>T | CA375249995 | ABL1 | c.1256A>T (p.Lys419Met) c.1199A>T (p.Lys400Met) | |
9 | g.130874982G>A | CA467395436 | ABL1 | c.1257G>A (p.Lys419=) c.1200G>A (p.Lys400=) | |
9 | g.130874982G>C | CA375249997 | ABL1 | c.1257G>C (p.Lys419Asn) c.1200G>C (p.Lys400Asn) | |
9 | g.130874982G>T | CA375249998 | ABL1 | c.1257G>T (p.Lys419Asn) c.1200G>T (p.Lys400Asn) | |
9 | g.130874983T>A | CA375249999 | ABL1 | c.1258T>A (p.Phe420Ile) c.1201T>A (p.Phe401Ile) |