Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.38070896G>ACA425864456CYP1B1c.1458C>T (p.Ile486=)
c.345C>T (p.Ile115=)
2g.38070896G>CCA346327115CYP1B1c.1458C>G (p.Ile486Met)
c.345C>G (p.Ile115Met)
2g.38070896G>TCA425864457CYP1B1c.1458C>A (p.Ile486=)
c.345C>A (p.Ile115=)
2g.38070897A>CCA346327116CYP1B1c.1457T>G (p.Ile486Ser)
c.344T>G (p.Ile115Ser)
2g.38070897A>GCA346327117CYP1B1c.1457T>C (p.Ile486Thr)
c.344T>C (p.Ile115Thr)
2g.38070897A>TCA346327118CYP1B1c.1457T>A (p.Ile486Asn)
c.344T>A (p.Ile115Asn)
2g.38070898T>ACA346327119CYP1B1c.1456A>T (p.Ile486Phe)
c.343A>T (p.Ile115Phe)
2g.38070898T>CCA1619777CYP1B1c.1456A>G (p.Ile486Val)
c.343A>G (p.Ile115Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.38070898T>GCA346327120CYP1B1c.1456A>C (p.Ile486Leu)
c.343A>C (p.Ile115Leu)
2g.38070898T=CA1245626006CYP1B1c.1456A= (p.Ile486=)
c.343A= (p.Ile115=)
2g.38070899G>ACA1619778CYP1B1c.1455C>T (p.Ser485=)
c.342C>T (p.Ser114=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.38070899G>CCA425864462CYP1B1c.1455C>G (p.Ser485=)
c.342C>G (p.Ser114=)
2g.38070899G=CA1245626007CYP1B1c.1455C= (p.Ser485=)
c.342C= (p.Ser114=)
2g.38070899G>TCA425864464CYP1B1c.1455C>A (p.Ser485=)
c.342C>A (p.Ser114=)
2g.38070900G>ACA346327121CYP1B1c.1454C>T (p.Ser485Phe)
c.341C>T (p.Ser114Phe)
2g.38070900G>CCA1619779CYP1B1c.1454C>G (p.Ser485Cys)
c.341C>G (p.Ser114Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.38070900G=CA1245626008CYP1B1c.1454C= (p.Ser485=)
c.341C= (p.Ser114=)
2g.38070900G>TCA346327122CYP1B1c.1454C>A (p.Ser485Tyr)
c.341C>A (p.Ser114Tyr)
2g.38070901A>CCA346327123CYP1B1c.1453T>G (p.Ser485Ala)
c.340T>G (p.Ser114Ala)
2g.38070901A>GCA346327124CYP1B1c.1453T>C (p.Ser485Pro)
c.340T>C (p.Ser114Pro)
2g.38070901A>TCA346327125CYP1B1c.1453T>A (p.Ser485Thr)
c.340T>A (p.Ser114Thr)
2g.38070902G>ACA425864467CYP1B1c.1452C>T (p.Ile484=)
c.339C>T (p.Ile113=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.38070902G>CCA346327126CYP1B1c.1452C>G (p.Ile484Met)
c.339C>G (p.Ile113Met)
2g.38070902G=CA1245626010CYP1B1c.1452C= (p.Ile484=)
c.339C= (p.Ile113=)
2g.38070902G>TCA425864466CYP1B1c.1452C>A (p.Ile484=)
c.339C>A (p.Ile113=)
2g.38070902_38070903delinsGACA1245626009CYP1B1c.1451_1452delinsTC (p.Ile484=)
c.338_339delinsTC (p.Ile113=)
2g.38070903delCA532236892CYP1B1c.1451del (p.Ile484ThrfsTer20)
c.338del (p.Ile113ThrfsTer20)
 dbSNP gnomAD v2 gnomAD v4
2g.38070903A=CA1245626011CYP1B1c.1451T= (p.Ile484=)
c.338T= (p.Ile113=)
2g.38070903A>CCA346327127CYP1B1c.1451T>G (p.Ile484Ser)
c.338T>G (p.Ile113Ser)
2g.38070903A>GCA346327128CYP1B1c.1451T>C (p.Ile484Thr)
c.338T>C (p.Ile113Thr)
 dbSNP gnomAD v2 gnomAD v4
2g.38070903A>TCA346327129CYP1B1c.1451T>A (p.Ile484Asn)
c.338T>A (p.Ile113Asn)
2g.38070904T>ACA346327130CYP1B1c.1450A>T (p.Ile484Phe)
c.337A>T (p.Ile113Phe)
2g.38070904T>CCA346327131CYP1B1c.1450A>G (p.Ile484Val)
c.337A>G (p.Ile113Val)
 dbSNP gnomAD v3 gnomAD v4
2g.38070904T>GCA346327132CYP1B1c.1450A>C (p.Ile484Leu)
c.337A>C (p.Ile113Leu)
2g.38070904T=CA1245626012CYP1B1c.1450A= (p.Ile484=)
c.337A= (p.Ile113=)
2g.38070905G>ACA425864471CYP1B1c.1449C>T (p.Phe483=)
c.336C>T (p.Phe112=)
2g.38070905G>CCA346327133CYP1B1c.1449C>G (p.Phe483Leu)
c.336C>G (p.Phe112Leu)
2g.38070905G>TCA346327134CYP1B1c.1449C>A (p.Phe483Leu)
c.336C>A (p.Phe112Leu)
2g.38070906A>CCA346327137CYP1B1c.1448T>G (p.Phe483Cys)
c.335T>G (p.Phe112Cys)
2g.38070906A>GCA346327136CYP1B1c.1448T>C (p.Phe483Ser)
c.335T>C (p.Phe112Ser)
2g.38070906A>TCA346327135CYP1B1c.1448T>A (p.Phe483Tyr)
c.335T>A (p.Phe112Tyr)
2g.38070907A=CA1245626013CYP1B1c.1447T= (p.Phe483=)
c.334T= (p.Phe112=)
2g.38070907A>CCA346327138CYP1B1c.1447T>G (p.Phe483Val)
c.334T>G (p.Phe112Val)
2g.38070907A>GCA346327139CYP1B1c.1447T>C (p.Phe483Leu)
c.334T>C (p.Phe112Leu)
 dbSNP gnomAD v2 gnomAD v4
2g.38070907A>TCA346327140CYP1B1c.1447T>A (p.Phe483Ile)
c.334T>A (p.Phe112Ile)
2g.38070908G>ACA425864474CYP1B1c.1446C>T (p.Leu482=)
c.333C>T (p.Leu111=)
2g.38070908G>CCA1619780CYP1B1c.1446C>G (p.Leu482=)
c.333C>G (p.Leu111=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.38070908G=CA1245626014CYP1B1c.1446C= (p.Leu482=)
c.333C= (p.Leu111=)
2g.38070908G>TCA425864475CYP1B1c.1446C>A (p.Leu482=)
c.333C>A (p.Leu111=)
2g.38070909A>CCA346327141CYP1B1c.1445T>G (p.Leu482Arg)
c.332T>G (p.Leu111Arg)

Number of alleles fetched