Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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= | |
X | g.74525858G>T | CA413658065 | SLC16A2 | c.1135G>T (p.Asp379Tyr) c.1044G>T c.575G>T | |
X | g.74525859A>C | CA413658067 | SLC16A2 | c.1136A>C (p.Asp379Ala) c.1045A>C c.576A>C | |
X | g.74525859A>G | CA413658069 | SLC16A2 | c.1136A>G (p.Asp379Gly) c.1045A>G c.576A>G | |
X | g.74525859A>T | CA413658068 | SLC16A2 | c.1136A>T (p.Asp379Val) c.1045A>T c.576A>T | |
X | g.74525860C>A | CA413658070 | SLC16A2 | c.1137C>A (p.Asp379Glu) c.1046C>A c.577C>A | |
X | g.74525860C>G | CA413658071 | SLC16A2 | c.1137C>G (p.Asp379Glu) c.1046C>G c.577C>G | |
X | g.74525860C>T | CA517241420 | SLC16A2 | c.1137C>T (p.Asp379=) c.1046C>T c.577C>T | |
X | g.74525861T>A | CA413658072 | SLC16A2 | c.1138T>A (p.Ser380Thr) c.1047T>A c.578T>A | dbSNP gnomAD v3 gnomAD v4 |
X | g.74525861T>C | CA413658073 | SLC16A2 | c.1138T>C (p.Ser380Pro) c.1047T>C c.578T>C | |
X | g.74525861T>G | CA413658074 | SLC16A2 | c.1138T>G (p.Ser380Ala) c.1047T>G c.578T>G | |
X | g.74525861T= | CA2437508456 | SLC16A2 | c.1138T= (p.Ser380=) c.1047T= c.578T= | |
X | g.74525862C>A | CA413658075 | SLC16A2 | c.1139C>A (p.Ser380Tyr) c.1048C>A c.579C>A | |
X | g.74525862C>G | CA413658076 | SLC16A2 | c.1139C>G (p.Ser380Cys) c.1048C>G c.579C>G | |
X | g.74525862C>T | CA413658077 | SLC16A2 | c.1139C>T (p.Ser380Phe) c.1048C>T c.579C>T | gnomAD v4 |
X | g.74525863C>A | CA517241432 | SLC16A2 | c.1140C>A (p.Ser380=) c.1049C>A c.580C>A | |
X | g.74525863C>G | CA517241438 | SLC16A2 | c.1140C>G (p.Ser380=) c.1049C>G c.580C>G | |
X | g.74525863C>T | CA517241435 | SLC16A2 | c.1140C>T (p.Ser380=) c.1049C>T c.580C>T | |
X | g.74525864A>C | CA413658078 | SLC16A2 | c.1141A>C (p.Ile381Leu) c.1050A>C c.581A>C | |
X | g.74525864A>G | CA413658079 | SLC16A2 | c.1141A>G (p.Ile381Val) c.1050A>G c.581A>G | |
X | g.74525864A>T | CA413658080 | SLC16A2 | c.1141A>T (p.Ile381Phe) c.1050A>T c.581A>T | COSMIC |
X | g.74525865T>A | CA413658083 | SLC16A2 | c.1142T>A (p.Ile381Asn) c.1051T>A c.582T>A | |
X | g.74525865T>C | CA413658081 | SLC16A2 | c.1142T>C (p.Ile381Thr) c.1051T>C c.582T>C | |
X | g.74525865T>G | CA413658082 | SLC16A2 | c.1142T>G (p.Ile381Ser) c.1051T>G c.582T>G | |
X | g.74525866C>A | CA517241446 | SLC16A2 | c.1143C>A (p.Ile381=) c.1052C>A c.583C>A | |
X | g.74525866C>G | CA413658084 | SLC16A2 | c.1143C>G (p.Ile381Met) c.1052C>G c.583C>G | |
X | g.74525866C>T | CA517241452 | SLC16A2 | c.1143C>T (p.Ile381=) c.1052C>T c.583C>T | |
X | g.74525867C>A | CA413658085 | SLC16A2 | c.1144C>A (p.Pro382Thr) c.1053C>A c.584C>A | |
X | g.74525867C>G | CA413658086 | SLC16A2 | c.1144C>G (p.Pro382Ala) c.1053C>G c.584C>G | |
X | g.74525867C>T | CA413658087 | SLC16A2 | c.1144C>T (p.Pro382Ser) c.1053C>T c.584C>T | ClinVar |
X | g.74525868C>A | CA413658088 | SLC16A2 | c.1145C>A (p.Pro382His) c.1054C>A c.585C>A | |
X | g.74525868C= | CA2437508457 | SLC16A2 | c.1145C= (p.Pro382=) c.1054C= c.585C= | |
X | g.74525868C>G | CA413658089 | SLC16A2 | c.1145C>G (p.Pro382Arg) c.1054C>G c.585C>G | |
X | g.74525868C>T | CA413658090 | SLC16A2 | c.1145C>T (p.Pro382Leu) c.1054C>T c.585C>T | ClinVar dbSNP gnomAD v4 |
X | g.74525869T>A | CA517241466 | SLC16A2 | c.1146T>A (p.Pro382=) c.1055T>A c.586T>A |