Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.74720630_74720644delCA2629506127CYP1A1c.1384_1398del (p.Ile462_Glu466del)
c.1297_1311del (p.Ile433_Glu437del)
c.1300_1314del (p.Ile434_Glu438del)
gnomAD v4
15g.74720642_74720646delinsAATGGCA2187814935CYP1A1c.1382_1386delinsCCATT (p.Thr461=)
c.1295_1299delinsCCATT (p.Thr432=)
c.1298_1302delinsCCATT (p.Thr433=)
15g.74720643_74720646delCA7659240CYP1A1c.1382_1385del (p.Thr461MetfsTer25)
c.1295_1298del (p.Thr432MetfsTer25)
c.1298_1301del (p.Thr433MetfsTer25)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.74720644T>ACA272812639CYP1A1c.1384A>T (p.Ile462Phe)
c.1297A>T (p.Ile433Phe)
c.1300A>T (p.Ile434Phe)
dbSNP
15g.74720644T>CCA7659241CYP1A1c.1384A>G (p.Ile462Val)
c.1297A>G (p.Ile433Val)
c.1300A>G (p.Ile434Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720644T>GCA272812640CYP1A1c.1384A>C (p.Ile462Leu)
c.1297A>C (p.Ile433Leu)
c.1300A>C (p.Ile434Leu)
dbSNP gnomAD v4
15g.74720644T=CA2187814937CYP1A1c.1384A= (p.Ile462=)
c.1297A= (p.Ile433=)
c.1300A= (p.Ile434=)
15g.74720645G>ACA491488170CYP1A1c.1383C>T (p.Thr461=)
c.1296C>T (p.Thr432=)
c.1299C>T (p.Thr433=)
gnomAD v4
15g.74720645G>CCA491488167CYP1A1c.1383C>G (p.Thr461=)
c.1296C>G (p.Thr432=)
c.1299C>G (p.Thr433=)
15g.74720645G>TCA491488168CYP1A1c.1383C>A (p.Thr461=)
c.1296C>A (p.Thr432=)
c.1299C>A (p.Thr433=)
15g.74720646G>ACA7659243CYP1A1c.1382C>T (p.Thr461Ile)
c.1295C>T (p.Thr432Ile)
c.1298C>T (p.Thr433Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720646G>CCA393164185CYP1A1c.1382C>G (p.Thr461Ser)
c.1295C>G (p.Thr432Ser)
c.1298C>G (p.Thr433Ser)
15g.74720646G=CA2187814938CYP1A1c.1382C= (p.Thr461=)
c.1295C= (p.Thr432=)
c.1298C= (p.Thr433=)
15g.74720646G>TCA7659242CYP1A1c.1382C>A (p.Thr461Asn)
c.1295C>A (p.Thr432Asn)
c.1298C>A (p.Thr433Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720647T>ACA393164187CYP1A1c.1381A>T (p.Thr461Ser)
c.1294A>T (p.Thr432Ser)
c.1297A>T (p.Thr433Ser)
15g.74720647T>CCA393164189CYP1A1c.1381A>G (p.Thr461Ala)
c.1294A>G (p.Thr432Ala)
c.1297A>G (p.Thr433Ala)
15g.74720647T>GCA393164191CYP1A1c.1381A>C (p.Thr461Pro)
c.1294A>C (p.Thr432Pro)
c.1297A>C (p.Thr433Pro)
15g.74720648C>ACA393164192CYP1A1c.1380G>T (p.Glu460Asp)
c.1293G>T (p.Glu431Asp)
c.1296G>T (p.Glu432Asp)
15g.74720648C>GCA393164193CYP1A1c.1380G>C (p.Glu460Asp)
c.1293G>C (p.Glu431Asp)
c.1296G>C (p.Glu432Asp)
15g.74720648C>TCA491488174CYP1A1c.1380G>A (p.Glu460=)
c.1293G>A (p.Glu431=)
c.1296G>A (p.Glu432=)
gnomAD v4
15g.74720649T>ACA393164195CYP1A1c.1379A>T (p.Glu460Val)
c.1292A>T (p.Glu431Val)
c.1295A>T (p.Glu432Val)
15g.74720649T>CCA393164196CYP1A1c.1379A>G (p.Glu460Gly)
c.1292A>G (p.Glu431Gly)
c.1295A>G (p.Glu432Gly)
15g.74720649T>GCA393164198CYP1A1c.1379A>C (p.Glu460Ala)
c.1292A>C (p.Glu431Ala)
c.1295A>C (p.Glu432Ala)
15g.74720650C>ACA393164200CYP1A1c.1378G>T (p.Glu460Ter)
c.1291G>T (p.Glu431Ter)
c.1294G>T (p.Glu432Ter)
15g.74720650C>GCA393164202CYP1A1c.1378G>C (p.Glu460Gln)
c.1291G>C (p.Glu431Gln)
c.1294G>C (p.Glu432Gln)
15g.74720650C>TCA393164204CYP1A1c.1378G>A (p.Glu460Lys)
c.1291G>A (p.Glu431Lys)
c.1294G>A (p.Glu432Lys)
COSMIC
15g.74720651A>CCA491488265CYP1A1c.1377T>G (p.Gly459=)
c.1290T>G (p.Gly430=)
c.1293T>G (p.Gly431=)
15g.74720651A>GCA491488262CYP1A1c.1377T>C (p.Gly459=)
c.1290T>C (p.Gly430=)
c.1293T>C (p.Gly431=)
15g.74720651A>TCA491488263CYP1A1c.1377T>A (p.Gly459=)
c.1290T>A (p.Gly430=)
c.1293T>A (p.Gly431=)
15g.74720652C>ACA393164207CYP1A1c.1376G>T (p.Gly459Val)
c.1289G>T (p.Gly430Val)
c.1292G>T (p.Gly431Val)
15g.74720652C>GCA393164209CYP1A1c.1376G>C (p.Gly459Ala)
c.1289G>C (p.Gly430Ala)
c.1292G>C (p.Gly431Ala)
15g.74720652C>TCA393164205CYP1A1c.1376G>A (p.Gly459Asp)
c.1289G>A (p.Gly430Asp)
c.1292G>A (p.Gly431Asp)
15g.74720653C>ACA393164210CYP1A1c.1375G>T (p.Gly459Cys)
c.1288G>T (p.Gly430Cys)
c.1291G>T (p.Gly431Cys)
15g.74720653C=CA2187814939CYP1A1c.1375G= (p.Gly459=)
c.1288G= (p.Gly430=)
c.1291G= (p.Gly431=)
15g.74720653C>GCA393164211CYP1A1c.1375G>C (p.Gly459Arg)
c.1288G>C (p.Gly430Arg)
c.1291G>C (p.Gly431Arg)
dbSNP
15g.74720653C>TCA7659244CYP1A1c.1375G>A (p.Gly459Ser)
c.1288G>A (p.Gly430Ser)
c.1291G>A (p.Gly431Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.74720654G>ACA7659245CYP1A1c.1374C>T (p.Ile458=)
c.1287C>T (p.Ile429=)
c.1290C>T (p.Ile430=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720654G>CCA393164215CYP1A1c.1374C>G (p.Ile458Met)
c.1287C>G (p.Ile429Met)
c.1290C>G (p.Ile430Met)
15g.74720654G=CA2187814940CYP1A1c.1374C= (p.Ile458=)
c.1287C= (p.Ile429=)
c.1290C= (p.Ile430=)
15g.74720654G>TCA491488266CYP1A1c.1374C>A (p.Ile458=)
c.1287C>A (p.Ile429=)
c.1290C>A (p.Ile430=)
15g.74720655A>CCA393164221CYP1A1c.1373T>G (p.Ile458Ser)
c.1286T>G (p.Ile429Ser)
c.1289T>G (p.Ile430Ser)
15g.74720655A>GCA393164219CYP1A1c.1373T>C (p.Ile458Thr)
c.1286T>C (p.Ile429Thr)
c.1289T>C (p.Ile430Thr)
dbSNP
15g.74720655A>TCA393164217CYP1A1c.1373T>A (p.Ile458Asn)
c.1286T>A (p.Ile429Asn)
c.1289T>A (p.Ile430Asn)
15g.74720656T>ACA393164222CYP1A1c.1372A>T (p.Ile458Phe)
c.1285A>T (p.Ile429Phe)
c.1288A>T (p.Ile430Phe)
15g.74720656T>CCA393164224CYP1A1c.1372A>G (p.Ile458Val)
c.1285A>G (p.Ile429Val)
c.1288A>G (p.Ile430Val)
15g.74720656T>GCA393164226CYP1A1c.1372A>C (p.Ile458Leu)
c.1285A>C (p.Ile429Leu)
c.1288A>C (p.Ile430Leu)
15g.74720656_74720657delinsTACA2187814941CYP1A1c.1371_1372delinsTA (p.Cys457=)
c.1284_1285delinsTA (p.Cys428=)
c.1287_1288delinsTA (p.Cys429=)
15g.74720657delCA7659246CYP1A1c.1371del (p.Cys457Ter)
c.1284del (p.Cys428Ter)
c.1287del (p.Cys429Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720657A=CA2187814942CYP1A1c.1371T= (p.Cys457=)
c.1284T= (p.Cys428=)
c.1287T= (p.Cys429=)
15g.74720657A>CCA393164228CYP1A1c.1371T>G (p.Cys457Trp)
c.1284T>G (p.Cys428Trp)
c.1287T>G (p.Cys429Trp)

Number of alleles fetched