Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.38070960A>CCA346327251CYP1B1c.1394T>G (p.Val465Gly)
c.281T>G (p.Val94Gly)
2g.38070960A>GCA346327252CYP1B1c.1394T>C (p.Val465Ala)
c.281T>C (p.Val94Ala)
 gnomAD v4
2g.38070960A>TCA346327253CYP1B1c.1394T>A (p.Val465Glu)
c.281T>A (p.Val94Glu)
 dbSNP
2g.38070961C>ACA346327254CYP1B1c.1393G>T (p.Val465Leu)
c.280G>T (p.Val94Leu)
2g.38070961C=CA1245626042CYP1B1c.1393G= (p.Val465=)
c.280G= (p.Val94=)
2g.38070961C>GCA346327255CYP1B1c.1393G>C (p.Val465Leu)
c.280G>C (p.Val94Leu)
2g.38070961C>TCA346327256CYP1B1c.1393G>A (p.Val465Met)
c.280G>A (p.Val94Met)
 dbSNP gnomAD v2 gnomAD v4
2g.38070962T>ACA1619791CYP1B1c.1392A>T (p.Ser464=)
c.279A>T (p.Ser93=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.38070962T>CCA425864325CYP1B1c.1392A>G (p.Ser464=)
c.279A>G (p.Ser93=)
2g.38070962T>GCA425864326CYP1B1c.1392A>C (p.Ser464=)
c.279A>C (p.Ser93=)
 gnomAD v4
2g.38070962T=CA1245626043CYP1B1c.1392A= (p.Ser464=)
c.279A= (p.Ser93=)
2g.38070963delCA2586969058CYP1B1c.1391del (p.Ser464Ter)
c.278del (p.Ser93Ter)
2g.38070963G>ACA346327257CYP1B1c.1391C>T (p.Ser464Leu)
c.278C>T (p.Ser93Leu)
2g.38070963G>CCA346327258CYP1B1c.1391C>G (p.Ser464Ter)
c.278C>G (p.Ser93Ter)
2g.38070963G=CA1245626044CYP1B1c.1391C= (p.Ser464=)
c.278C= (p.Ser93=)
2g.38070963G>TCA346327259CYP1B1c.1391C>A (p.Ser464Ter)
c.278C>A (p.Ser93Ter)
2g.38070964A>CCA346327261CYP1B1c.1390T>G (p.Ser464Ala)
c.277T>G (p.Ser93Ala)
2g.38070964A>GCA346327262CYP1B1c.1390T>C (p.Ser464Pro)
c.277T>C (p.Ser93Pro)
2g.38070964A>TCA346327260CYP1B1c.1390T>A (p.Ser464Thr)
c.277T>A (p.Ser93Thr)
 gnomAD v4
2g.38070969dupCA1619792CYP1B1c.1390dup (p.Ser464PhefsTer14)
c.277dup (p.Ser93PhefsTer14)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.38070965A>CCA346327264CYP1B1c.1389T>G (p.Phe463Leu)
c.276T>G (p.Phe92Leu)
2g.38070965A>GCA425864330CYP1B1c.1389T>C (p.Phe463=)
c.276T>C (p.Phe92=)
 ClinVar
2g.38070965A>TCA346327263CYP1B1c.1389T>A (p.Phe463Leu)
c.276T>A (p.Phe92Leu)
2g.38070966A>CCA346327265CYP1B1c.1388T>G (p.Phe463Cys)
c.275T>G (p.Phe92Cys)
2g.38070966A>GCA346327266CYP1B1c.1388T>C (p.Phe463Ser)
c.275T>C (p.Phe92Ser)
2g.38070966A>TCA346327267CYP1B1c.1388T>A (p.Phe463Tyr)
c.275T>A (p.Phe92Tyr)
2g.38070967A>CCA346327268CYP1B1c.1387T>G (p.Phe463Val)
c.274T>G (p.Phe92Val)
2g.38070967A>GCA346327269CYP1B1c.1387T>C (p.Phe463Leu)
c.274T>C (p.Phe92Leu)
2g.38070967A>TCA346327270CYP1B1c.1387T>A (p.Phe463Ile)
c.274T>A (p.Phe92Ile)
2g.38070968A=CA1245626045CYP1B1c.1386T= (p.Ile462=)
c.273T= (p.Ile91=)
2g.38070968A>CCA346327271CYP1B1c.1386T>G (p.Ile462Met)
c.273T>G (p.Ile91Met)
2g.38070968A>GCA425864333CYP1B1c.1386T>C (p.Ile462=)
c.273T>C (p.Ile91=)
 dbSNP
2g.38070968A>TCA425864335CYP1B1c.1386T>A (p.Ile462=)
c.273T>A (p.Ile91=)
2g.38070969A=CA1245626046CYP1B1c.1385T= (p.Ile462=)
c.272T= (p.Ile91=)
2g.38070969A>CCA346327272CYP1B1c.1385T>G (p.Ile462Ser)
c.272T>G (p.Ile91Ser)
2g.38070969A>GCA1619793CYP1B1c.1385T>C (p.Ile462Thr)
c.272T>C (p.Ile91Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.38070969A>TCA346327273CYP1B1c.1385T>A (p.Ile462Asn)
c.272T>A (p.Ile91Asn)
2g.38070970T>ACA346327274CYP1B1c.1384A>T (p.Ile462Phe)
c.271A>T (p.Ile91Phe)
2g.38070970T>CCA346327275CYP1B1c.1384A>G (p.Ile462Val)
c.271A>G (p.Ile91Val)
2g.38070970T>GCA346327276CYP1B1c.1384A>C (p.Ile462Leu)
c.271A>C (p.Ile91Leu)
2g.38070971C>ACA346327277CYP1B1c.1383G>T (p.Met461Ile)
c.270G>T (p.Met90Ile)
2g.38070971C=CA1245626047CYP1B1c.1383G= (p.Met461=)
c.270G= (p.Met90=)
2g.38070971C>GCA1619794CYP1B1c.1383G>C (p.Met461Ile)
c.270G>C (p.Met90Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.38070971C>TCA346327278CYP1B1c.1383G>A (p.Met461Ile)
c.270G>A (p.Met90Ile)
2g.38070972A=CA1245626048CYP1B1c.1382T= (p.Met461=)
c.269T= (p.Met90=)
2g.38070972A>CCA346327279CYP1B1c.1382T>G (p.Met461Arg)
c.269T>G (p.Met90Arg)
2g.38070972A>GCA1619795CYP1B1c.1382T>C (p.Met461Thr)
c.269T>C (p.Met90Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.38070972A>TCA346327280CYP1B1c.1382T>A (p.Met461Lys)
c.269T>A (p.Met90Lys)
2g.38070973T>ACA346327281CYP1B1c.1381A>T (p.Met461Leu)
c.268A>T (p.Met90Leu)
2g.38070973T>CCA45506039CYP1B1c.1381A>G (p.Met461Val)
c.268A>G (p.Met90Val)
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched