Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.74525838_74525844dup | CA2695234519 | SLC16A2 | c.1115_1121dup (p.Gly375CysfsTer7) c.1024_1030dup c.555_561dup | |
X | g.74525844C>A | CA255948 | SLC16A2 | c.1121C>A (p.Ser374Ter) c.1030C>A c.561C>A | ClinVar dbSNP |
X | g.74525844C= | CA2437508452 | SLC16A2 | c.1121C= (p.Ser374=) c.1030C= c.561C= | |
X | g.74525844C>G | CA413658033 | SLC16A2 | c.1121C>G (p.Ser374Ter) c.1030C>G c.561C>G | COSMIC |
X | g.74525844C>T | CA413658034 | SLC16A2 | c.1121C>T (p.Ser374Leu) c.1030C>T c.561C>T | |
X | g.74525844_74525845insGCCC | CA658820746 | SLC16A2 | c.1121_1122insGCCC (p.Gly375ProfsTer6) c.1030_1031insGCCC c.561_562insGCCC | |
X | g.74525845A>C | CA517241373 | SLC16A2 | c.1122A>C (p.Ser374=) c.1031A>C c.562A>C | |
X | g.74525845A>G | CA517241371 | SLC16A2 | c.1122A>G (p.Ser374=) c.1031A>G c.562A>G | |
X | g.74525845A>T | CA517241370 | SLC16A2 | c.1122A>T (p.Ser374=) c.1031A>T c.562A>T | |
X | g.74525846G>A | CA413658035 | SLC16A2 | c.1123G>A (p.Gly375Ser) c.1032G>A c.563G>A | |
X | g.74525846G>C | CA413658036 | SLC16A2 | c.1123G>C (p.Gly375Arg) c.1032G>C c.563G>C | |
X | g.74525846G>T | CA413658037 | SLC16A2 | c.1123G>T (p.Gly375Cys) c.1032G>T c.563G>T | |
X | g.74525847G>A | CA413658038 | SLC16A2 | c.1124G>A (p.Gly375Asp) c.1033G>A c.564G>A | |
X | g.74525847G>C | CA413658039 | SLC16A2 | c.1124G>C (p.Gly375Ala) c.1033G>C c.564G>C | |
X | g.74525847G>T | CA413658040 | SLC16A2 | c.1124G>T (p.Gly375Val) c.1033G>T c.564G>T | |
X | g.74525848C>A | CA517241379 | SLC16A2 | c.1125C>A (p.Gly375=) c.1034C>A c.565C>A | |
X | g.74525848C>G | CA517241381 | SLC16A2 | c.1125C>G (p.Gly375=) c.1034C>G c.565C>G | |
X | g.74525848C>T | CA517241380 | SLC16A2 | c.1125C>T (p.Gly375=) c.1034C>T c.565C>T | |
X | g.74525849C>A | CA413658041 | SLC16A2 | c.1126C>A (p.His376Asn) c.1035C>A c.566C>A | |
X | g.74525849C>G | CA413658042 | SLC16A2 | c.1126C>G (p.His376Asp) c.1035C>G c.566C>G | |
X | g.74525849C>T | CA413658043 | SLC16A2 | c.1126C>T (p.His376Tyr) c.1035C>T c.566C>T | |
X | g.74525850A>C | CA413658046 | SLC16A2 | c.1127A>C (p.His376Pro) c.1036A>C c.567A>C | |
X | g.74525850A>G | CA413658044 | SLC16A2 | c.1127A>G (p.His376Arg) c.1036A>G c.567A>G | gnomAD v3 gnomAD v4 |
X | g.74525850A>T | CA413658045 | SLC16A2 | c.1127A>T (p.His376Leu) c.1036A>T c.567A>T | |
X | g.74525851C>A | CA413658047 | SLC16A2 | c.1128C>A (p.His376Gln) c.1037C>A c.568C>A | |
X | g.74525851C>G | CA413658048 | SLC16A2 | c.1128C>G (p.His376Gln) c.1037C>G c.568C>G | |
X | g.74525851C>T | CA517241389 | SLC16A2 | c.1128C>T (p.His376=) c.1037C>T c.568C>T | gnomAD v3 gnomAD v4 |
X | g.74525852A>C | CA413658049 | SLC16A2 | c.1129A>C (p.Ile377Leu) c.1038A>C c.569A>C | |
X | g.74525852A>G | CA413658050 | SLC16A2 | c.1129A>G (p.Ile377Val) c.1038A>G c.569A>G | gnomAD v3 gnomAD v4 |
X | g.74525852A>T | CA413658051 | SLC16A2 | c.1129A>T (p.Ile377Phe) c.1038A>T c.569A>T | |
X | g.74525853T>A | CA413658052 | SLC16A2 | c.1130T>A (p.Ile377Asn) c.1039T>A c.570T>A | |
X | g.74525853T>C | CA413658053 | SLC16A2 | c.1130T>C (p.Ile377Thr) c.1039T>C c.570T>C | dbSNP gnomAD v4 |
X | g.74525853T>G | CA413658054 | SLC16A2 | c.1130T>G (p.Ile377Ser) c.1039T>G c.570T>G | |
X | g.74525853T= | CA2437508453 | SLC16A2 | c.1130T= (p.Ile377=) c.1039T= c.570T= | |
X | g.74525854C>A | CA517241396 | SLC16A2 | c.1131C>A (p.Ile377=) c.1040C>A c.571C>A | |
X | g.74525854C= | CA2437508454 | SLC16A2 | c.1131C= (p.Ile377=) c.1040C= c.571C= | |
X | g.74525854C>G | CA413658055 | SLC16A2 | c.1131C>G (p.Ile377Met) c.1040C>G c.571C>G | dbSNP gnomAD v2 gnomAD v4 |
X | g.74525854C>T | CA517241399 | SLC16A2 | c.1131C>T (p.Ile377=) c.1040C>T c.571C>T | gnomAD v4 |
X | g.74525855A>C | CA413658056 | SLC16A2 | c.1132A>C (p.Ser378Arg) c.1041A>C c.572A>C | ClinVar dbSNP |
X | g.74525855A>G | CA413658057 | SLC16A2 | c.1132A>G (p.Ser378Gly) c.1041A>G c.572A>G | |
X | g.74525855A>T | CA413658058 | SLC16A2 | c.1132A>T (p.Ser378Cys) c.1041A>T c.572A>T | COSMIC |
X | g.74525856G>A | CA413658060 | SLC16A2 | c.1133G>A (p.Ser378Asn) c.1042G>A c.573G>A | |
X | g.74525856G>C | CA413658061 | SLC16A2 | c.1133G>C (p.Ser378Thr) c.1042G>C c.573G>C | |
X | g.74525856G>T | CA413658059 | SLC16A2 | c.1133G>T (p.Ser378Ile) c.1042G>T c.573G>T | |
X | g.74525857T>A | CA413658062 | SLC16A2 | c.1134T>A (p.Ser378Arg) c.1043T>A c.574T>A | |
X | g.74525857T>C | CA517241408 | SLC16A2 | c.1134T>C (p.Ser378=) c.1043T>C c.574T>C | |
X | g.74525857T>G | CA413658063 | SLC16A2 | c.1134T>G (p.Ser378Arg) c.1043T>G c.574T>G | |
X | g.74525858G>A | CA413658064 | SLC16A2 | c.1135G>A (p.Asp379Asn) c.1044G>A c.575G>A | ClinVar dbSNP gnomAD v2 |
X | g.74525858G>C | CA413658066 | SLC16A2 | c.1135G>C (p.Asp379His) c.1044G>C c.575G>C | |
X | g.74525858G= | CA2437508455 | SLC16A2 | c.1135G= (p.Asp379=) c.1044G= c.575G= |