Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.74720630_74720644del | CA2629506127 | CYP1A1 | c.1384_1398del (p.Ile462_Glu466del) c.1297_1311del (p.Ile433_Glu437del) c.1300_1314del (p.Ile434_Glu438del) | gnomAD v4 |
15 | g.74720642_74720646delinsAATGG | CA2187814935 | CYP1A1 | c.1382_1386delinsCCATT (p.Thr461=) c.1295_1299delinsCCATT (p.Thr432=) c.1298_1302delinsCCATT (p.Thr433=) | |
15 | g.74720643_74720646del | CA7659240 | CYP1A1 | c.1382_1385del (p.Thr461MetfsTer25) c.1295_1298del (p.Thr432MetfsTer25) c.1298_1301del (p.Thr433MetfsTer25) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.74720644T>A | CA272812639 | CYP1A1 | c.1384A>T (p.Ile462Phe) c.1297A>T (p.Ile433Phe) c.1300A>T (p.Ile434Phe) | dbSNP |
15 | g.74720644T>C | CA7659241 | CYP1A1 | c.1384A>G (p.Ile462Val) c.1297A>G (p.Ile433Val) c.1300A>G (p.Ile434Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74720644T>G | CA272812640 | CYP1A1 | c.1384A>C (p.Ile462Leu) c.1297A>C (p.Ile433Leu) c.1300A>C (p.Ile434Leu) | dbSNP gnomAD v4 |
15 | g.74720644T= | CA2187814937 | CYP1A1 | c.1384A= (p.Ile462=) c.1297A= (p.Ile433=) c.1300A= (p.Ile434=) | |
15 | g.74720645G>A | CA491488170 | CYP1A1 | c.1383C>T (p.Thr461=) c.1296C>T (p.Thr432=) c.1299C>T (p.Thr433=) | gnomAD v4 |
15 | g.74720645G>C | CA491488167 | CYP1A1 | c.1383C>G (p.Thr461=) c.1296C>G (p.Thr432=) c.1299C>G (p.Thr433=) | |
15 | g.74720645G>T | CA491488168 | CYP1A1 | c.1383C>A (p.Thr461=) c.1296C>A (p.Thr432=) c.1299C>A (p.Thr433=) | |
15 | g.74720646G>A | CA7659243 | CYP1A1 | c.1382C>T (p.Thr461Ile) c.1295C>T (p.Thr432Ile) c.1298C>T (p.Thr433Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74720646G>C | CA393164185 | CYP1A1 | c.1382C>G (p.Thr461Ser) c.1295C>G (p.Thr432Ser) c.1298C>G (p.Thr433Ser) | |
15 | g.74720646G= | CA2187814938 | CYP1A1 | c.1382C= (p.Thr461=) c.1295C= (p.Thr432=) c.1298C= (p.Thr433=) | |
15 | g.74720646G>T | CA7659242 | CYP1A1 | c.1382C>A (p.Thr461Asn) c.1295C>A (p.Thr432Asn) c.1298C>A (p.Thr433Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74720647T>A | CA393164187 | CYP1A1 | c.1381A>T (p.Thr461Ser) c.1294A>T (p.Thr432Ser) c.1297A>T (p.Thr433Ser) | |
15 | g.74720647T>C | CA393164189 | CYP1A1 | c.1381A>G (p.Thr461Ala) c.1294A>G (p.Thr432Ala) c.1297A>G (p.Thr433Ala) | |
15 | g.74720647T>G | CA393164191 | CYP1A1 | c.1381A>C (p.Thr461Pro) c.1294A>C (p.Thr432Pro) c.1297A>C (p.Thr433Pro) | |
15 | g.74720648C>A | CA393164192 | CYP1A1 | c.1380G>T (p.Glu460Asp) c.1293G>T (p.Glu431Asp) c.1296G>T (p.Glu432Asp) | |
15 | g.74720648C>G | CA393164193 | CYP1A1 | c.1380G>C (p.Glu460Asp) c.1293G>C (p.Glu431Asp) c.1296G>C (p.Glu432Asp) | |
15 | g.74720648C>T | CA491488174 | CYP1A1 | c.1380G>A (p.Glu460=) c.1293G>A (p.Glu431=) c.1296G>A (p.Glu432=) | gnomAD v4 |
15 | g.74720649T>A | CA393164195 | CYP1A1 | c.1379A>T (p.Glu460Val) c.1292A>T (p.Glu431Val) c.1295A>T (p.Glu432Val) | |
15 | g.74720649T>C | CA393164196 | CYP1A1 | c.1379A>G (p.Glu460Gly) c.1292A>G (p.Glu431Gly) c.1295A>G (p.Glu432Gly) | |
15 | g.74720649T>G | CA393164198 | CYP1A1 | c.1379A>C (p.Glu460Ala) c.1292A>C (p.Glu431Ala) c.1295A>C (p.Glu432Ala) | |
15 | g.74720650C>A | CA393164200 | CYP1A1 | c.1378G>T (p.Glu460Ter) c.1291G>T (p.Glu431Ter) c.1294G>T (p.Glu432Ter) | |
15 | g.74720650C>G | CA393164202 | CYP1A1 | c.1378G>C (p.Glu460Gln) c.1291G>C (p.Glu431Gln) c.1294G>C (p.Glu432Gln) | |
15 | g.74720650C>T | CA393164204 | CYP1A1 | c.1378G>A (p.Glu460Lys) c.1291G>A (p.Glu431Lys) c.1294G>A (p.Glu432Lys) | COSMIC |
15 | g.74720651A>C | CA491488265 | CYP1A1 | c.1377T>G (p.Gly459=) c.1290T>G (p.Gly430=) c.1293T>G (p.Gly431=) | |
15 | g.74720651A>G | CA491488262 | CYP1A1 | c.1377T>C (p.Gly459=) c.1290T>C (p.Gly430=) c.1293T>C (p.Gly431=) | |
15 | g.74720651A>T | CA491488263 | CYP1A1 | c.1377T>A (p.Gly459=) c.1290T>A (p.Gly430=) c.1293T>A (p.Gly431=) | |
15 | g.74720652C>A | CA393164207 | CYP1A1 | c.1376G>T (p.Gly459Val) c.1289G>T (p.Gly430Val) c.1292G>T (p.Gly431Val) | |
15 | g.74720652C>G | CA393164209 | CYP1A1 | c.1376G>C (p.Gly459Ala) c.1289G>C (p.Gly430Ala) c.1292G>C (p.Gly431Ala) | |
15 | g.74720652C>T | CA393164205 | CYP1A1 | c.1376G>A (p.Gly459Asp) c.1289G>A (p.Gly430Asp) c.1292G>A (p.Gly431Asp) | |
15 | g.74720653C>A | CA393164210 | CYP1A1 | c.1375G>T (p.Gly459Cys) c.1288G>T (p.Gly430Cys) c.1291G>T (p.Gly431Cys) | |
15 | g.74720653C= | CA2187814939 | CYP1A1 | c.1375G= (p.Gly459=) c.1288G= (p.Gly430=) c.1291G= (p.Gly431=) | |
15 | g.74720653C>G | CA393164211 | CYP1A1 | c.1375G>C (p.Gly459Arg) c.1288G>C (p.Gly430Arg) c.1291G>C (p.Gly431Arg) | dbSNP |
15 | g.74720653C>T | CA7659244 | CYP1A1 | c.1375G>A (p.Gly459Ser) c.1288G>A (p.Gly430Ser) c.1291G>A (p.Gly431Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.74720654G>A | CA7659245 | CYP1A1 | c.1374C>T (p.Ile458=) c.1287C>T (p.Ile429=) c.1290C>T (p.Ile430=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74720654G>C | CA393164215 | CYP1A1 | c.1374C>G (p.Ile458Met) c.1287C>G (p.Ile429Met) c.1290C>G (p.Ile430Met) | |
15 | g.74720654G= | CA2187814940 | CYP1A1 | c.1374C= (p.Ile458=) c.1287C= (p.Ile429=) c.1290C= (p.Ile430=) | |
15 | g.74720654G>T | CA491488266 | CYP1A1 | c.1374C>A (p.Ile458=) c.1287C>A (p.Ile429=) c.1290C>A (p.Ile430=) | |
15 | g.74720655A>C | CA393164221 | CYP1A1 | c.1373T>G (p.Ile458Ser) c.1286T>G (p.Ile429Ser) c.1289T>G (p.Ile430Ser) | |
15 | g.74720655A>G | CA393164219 | CYP1A1 | c.1373T>C (p.Ile458Thr) c.1286T>C (p.Ile429Thr) c.1289T>C (p.Ile430Thr) | dbSNP |
15 | g.74720655A>T | CA393164217 | CYP1A1 | c.1373T>A (p.Ile458Asn) c.1286T>A (p.Ile429Asn) c.1289T>A (p.Ile430Asn) | |
15 | g.74720656T>A | CA393164222 | CYP1A1 | c.1372A>T (p.Ile458Phe) c.1285A>T (p.Ile429Phe) c.1288A>T (p.Ile430Phe) | |
15 | g.74720656T>C | CA393164224 | CYP1A1 | c.1372A>G (p.Ile458Val) c.1285A>G (p.Ile429Val) c.1288A>G (p.Ile430Val) | |
15 | g.74720656T>G | CA393164226 | CYP1A1 | c.1372A>C (p.Ile458Leu) c.1285A>C (p.Ile429Leu) c.1288A>C (p.Ile430Leu) | |
15 | g.74720656_74720657delinsTA | CA2187814941 | CYP1A1 | c.1371_1372delinsTA (p.Cys457=) c.1284_1285delinsTA (p.Cys428=) c.1287_1288delinsTA (p.Cys429=) | |
15 | g.74720657del | CA7659246 | CYP1A1 | c.1371del (p.Cys457Ter) c.1284del (p.Cys428Ter) c.1287del (p.Cys429Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74720657A= | CA2187814942 | CYP1A1 | c.1371T= (p.Cys457=) c.1284T= (p.Cys428=) c.1287T= (p.Cys429=) | |
15 | g.74720657A>C | CA393164228 | CYP1A1 | c.1371T>G (p.Cys457Trp) c.1284T>G (p.Cys428Trp) c.1287T>G (p.Cys429Trp) |