Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.74720545dupCA619412588CYP1A1c.1485dup (p.Leu496AlafsTer9)
c.1398dup (p.Leu467AlafsTer9)
c.1401dup (p.Leu468AlafsTer9)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.74720544C>ACA393163812CYP1A1c.1484G>T (p.Gly495Val)
c.1397G>T (p.Gly466Val)
c.1400G>T (p.Gly467Val)
15g.74720544C>GCA393163814CYP1A1c.1484G>C (p.Gly495Ala)
c.1397G>C (p.Gly466Ala)
c.1400G>C (p.Gly467Ala)
15g.74720544C>TCA393163815CYP1A1c.1484G>A (p.Gly495Glu)
c.1397G>A (p.Gly466Glu)
c.1400G>A (p.Gly467Glu)
15g.74720545C>ACA7659204CYP1A1c.1483G>T (p.Gly495Trp)
c.1396G>T (p.Gly466Trp)
c.1399G>T (p.Gly467Trp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720545C=CA2187814879CYP1A1c.1483G= (p.Gly495=)
c.1396G= (p.Gly466=)
c.1399G= (p.Gly467=)
15g.74720545C>GCA393163816CYP1A1c.1483G>C (p.Gly495Arg)
c.1396G>C (p.Gly466Arg)
c.1399G>C (p.Gly467Arg)
15g.74720545C>TCA393163818CYP1A1c.1483G>A (p.Gly495Arg)
c.1396G>A (p.Gly466Arg)
c.1399G>A (p.Gly467Arg)
15g.74720546A>CCA393163820CYP1A1c.1482T>G (p.Tyr494Ter)
c.1395T>G (p.Tyr465Ter)
c.1398T>G (p.Tyr466Ter)
15g.74720546A>GCA491488031CYP1A1c.1482T>C (p.Tyr494=)
c.1395T>C (p.Tyr465=)
c.1398T>C (p.Tyr466=)
15g.74720546A>TCA393163821CYP1A1c.1482T>A (p.Tyr494Ter)
c.1395T>A (p.Tyr465Ter)
c.1398T>A (p.Tyr466Ter)
15g.74720547T>ACA393163826CYP1A1c.1481A>T (p.Tyr494Phe)
c.1394A>T (p.Tyr465Phe)
c.1397A>T (p.Tyr466Phe)
15g.74720547T>CCA7659205CYP1A1c.1481A>G (p.Tyr494Cys)
c.1394A>G (p.Tyr465Cys)
c.1397A>G (p.Tyr466Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720547T>GCA393163823CYP1A1c.1481A>C (p.Tyr494Ser)
c.1394A>C (p.Tyr465Ser)
c.1397A>C (p.Tyr466Ser)
15g.74720547T=CA2187814880CYP1A1c.1481A= (p.Tyr494=)
c.1394A= (p.Tyr465=)
c.1397A= (p.Tyr466=)
15g.74720547_74720548insGAATTAGGCAATAAGGGTATCAAGTGAATATAGTACCA2629505950CYP1A1c.1480_1481insGTACTATATTCACTTGATACCCTTATTGCCTAATTC (p.Tyr494CysfsTer6)
c.1393_1394insGTACTATATTCACTTGATACCCTTATTGCCTAATTC (p.Tyr465CysfsTer6)
c.1396_1397insGTACTATATTCACTTGATACCCTTATTGCCTAATTC (p.Tyr466CysfsTer6)
gnomAD v4
15g.74720548A>CCA393163828CYP1A1c.1480T>G (p.Tyr494Asp)
c.1393T>G (p.Tyr465Asp)
c.1396T>G (p.Tyr466Asp)
15g.74720548A>GCA393163830CYP1A1c.1480T>C (p.Tyr494His)
c.1393T>C (p.Tyr465His)
c.1396T>C (p.Tyr466His)
15g.74720548A>TCA393163831CYP1A1c.1480T>A (p.Tyr494Asn)
c.1393T>A (p.Tyr465Asn)
c.1396T>A (p.Tyr466Asn)
15g.74720549G>ACA491488033CYP1A1c.1479C>T (p.Ile493=)
c.1392C>T (p.Ile464=)
c.1395C>T (p.Ile465=)
dbSNP
15g.74720549G>CCA393163832CYP1A1c.1479C>G (p.Ile493Met)
c.1392C>G (p.Ile464Met)
c.1395C>G (p.Ile465Met)
15g.74720549G=CA2187814881CYP1A1c.1479C= (p.Ile493=)
c.1392C= (p.Ile464=)
c.1395C= (p.Ile465=)
15g.74720549G>TCA491488034CYP1A1c.1479C>A (p.Ile493=)
c.1392C>A (p.Ile464=)
c.1395C>A (p.Ile465=)
15g.74720550A>CCA393163835CYP1A1c.1478T>G (p.Ile493Ser)
c.1391T>G (p.Ile464Ser)
c.1394T>G (p.Ile465Ser)
15g.74720550A>GCA393163836CYP1A1c.1478T>C (p.Ile493Thr)
c.1391T>C (p.Ile464Thr)
c.1394T>C (p.Ile465Thr)
15g.74720550A>TCA393163838CYP1A1c.1478T>A (p.Ile493Asn)
c.1391T>A (p.Ile464Asn)
c.1394T>A (p.Ile465Asn)
15g.74720551T>ACA393163839CYP1A1c.1477A>T (p.Ile493Phe)
c.1390A>T (p.Ile464Phe)
c.1393A>T (p.Ile465Phe)
15g.74720551T>CCA393163841CYP1A1c.1477A>G (p.Ile493Val)
c.1390A>G (p.Ile464Val)
c.1393A>G (p.Ile465Val)
gnomAD v4
15g.74720551T>GCA393163843CYP1A1c.1477A>C (p.Ile493Leu)
c.1390A>C (p.Ile464Leu)
c.1393A>C (p.Ile465Leu)
15g.74720552G>ACA491488037CYP1A1c.1476C>T (p.Pro492=)
c.1389C>T (p.Pro463=)
c.1392C>T (p.Pro464=)
15g.74720552G>CCA491488038CYP1A1c.1476C>G (p.Pro492=)
c.1389C>G (p.Pro463=)
c.1392C>G (p.Pro464=)
15g.74720552G>TCA491488039CYP1A1c.1476C>A (p.Pro492=)
c.1389C>A (p.Pro463=)
c.1392C>A (p.Pro464=)
15g.74720556delCA645590700CYP1A1c.1476del (p.Ile493SerfsTer4)
c.1389del (p.Ile464SerfsTer4)
c.1392del (p.Ile465SerfsTer4)
gnomAD v4 COSMIC
15g.74720553G>ACA393163845CYP1A1c.1475C>T (p.Pro492Leu)
c.1388C>T (p.Pro463Leu)
c.1391C>T (p.Pro464Leu)
15g.74720553G>CCA7659206CYP1A1c.1475C>G (p.Pro492Arg)
c.1388C>G (p.Pro463Arg)
c.1391C>G (p.Pro464Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720553G=CA2187814882CYP1A1c.1475C= (p.Pro492=)
c.1388C= (p.Pro463=)
c.1391C= (p.Pro464=)
15g.74720553G>TCA393163847CYP1A1c.1475C>A (p.Pro492His)
c.1388C>A (p.Pro463His)
c.1391C>A (p.Pro464His)
15g.74720554G>ACA393163849CYP1A1c.1474C>T (p.Pro492Ser)
c.1387C>T (p.Pro463Ser)
c.1390C>T (p.Pro464Ser)
gnomAD v4
15g.74720554G>CCA393163852CYP1A1c.1474C>G (p.Pro492Ala)
c.1387C>G (p.Pro463Ala)
c.1390C>G (p.Pro464Ala)
15g.74720554G>TCA393163851CYP1A1c.1474C>A (p.Pro492Thr)
c.1387C>A (p.Pro463Thr)
c.1390C>A (p.Pro464Thr)
15g.74720555G>ACA7659207CYP1A1c.1473C>T (p.Thr491=)
c.1386C>T (p.Thr462=)
c.1389C>T (p.Thr463=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.74720555G>CCA491488041CYP1A1c.1473C>G (p.Thr491=)
c.1386C>G (p.Thr462=)
c.1389C>G (p.Thr463=)
15g.74720555G=CA2187814883CYP1A1c.1473C= (p.Thr491=)
c.1386C= (p.Thr462=)
c.1389C= (p.Thr463=)
15g.74720555G>TCA491488042CYP1A1c.1473C>A (p.Thr491=)
c.1386C>A (p.Thr462=)
c.1389C>A (p.Thr463=)
gnomAD v4
15g.74720556G>ACA393163855CYP1A1c.1472C>T (p.Thr491Ile)
c.1385C>T (p.Thr462Ile)
c.1388C>T (p.Thr463Ile)
gnomAD v4
15g.74720556G>CCA393163856CYP1A1c.1472C>G (p.Thr491Ser)
c.1385C>G (p.Thr462Ser)
c.1388C>G (p.Thr463Ser)
15g.74720556G=CA2187814884CYP1A1c.1472C= (p.Thr491=)
c.1385C= (p.Thr462=)
c.1388C= (p.Thr463=)
15g.74720556G>TCA7659208CYP1A1c.1472C>A (p.Thr491Asn)
c.1385C>A (p.Thr462Asn)
c.1388C>A (p.Thr463Asn)
dbSNP ExAC gnomAD v4
15g.74720557T>ACA393163858CYP1A1c.1471A>T (p.Thr491Ser)
c.1384A>T (p.Thr462Ser)
c.1387A>T (p.Thr463Ser)
15g.74720557T>CCA393163859CYP1A1c.1471A>G (p.Thr491Ala)
c.1384A>G (p.Thr462Ala)
c.1387A>G (p.Thr463Ala)
dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched