Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21007402T>ACA345989924APOBc.9466A>T (p.Thr3156Ser)
c.5869+3331A>T (n.5869+3331A>T)
2g.21007402T>CCA345989926APOBc.9466A>G (p.Thr3156Ala)
c.5869+3331A>G (n.5869+3331A>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21007402T>GCA345989927APOBc.9466A>C (p.Thr3156Pro)
c.5869+3331A>C (n.5869+3331A>C)
2g.21007402T=CA2493475234APOBc.9466A= (p.Thr3156=)
c.5869+3331A= (n.5869+3331A=)
2g.21007407dupCA531312729APOBc.9466dup (p.Thr3156AsnfsTer15)
c.5869+3331dup (n.5869+3331dup)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21007407delCA2658076738APOBc.9466del (p.Thr3156GlnfsTer3)
c.5869+3331del (n.5869+3331del)
gnomAD v4
2g.21007402_21007403insACA425344270APOBc.9465_9466insT (p.Thr3156TyrfsTer15)
c.5869+3330_5869+3331insT (n.5869+3330_5869+3331insT)
2g.21007403T>ACA345989930APOBc.9465A>T (p.Lys3155Asn)
c.5869+3330A>T (n.5869+3330A>T)
2g.21007403T>CCA425344269APOBc.9465A>G (p.Lys3155=)
c.5869+3330A>G (n.5869+3330A>G)
COSMIC
2g.21007403T>GCA345989932APOBc.9465A>C (p.Lys3155Asn)
c.5869+3330A>C (n.5869+3330A>C)
2g.21007404T>ACA345989934APOBc.9464A>T (p.Lys3155Ile)
c.5869+3329A>T (n.5869+3329A>T)
2g.21007404T>CCA066558APOBc.9464A>G (p.Lys3155Arg)
c.5869+3329A>G (n.5869+3329A>G)
dbSNP ExAC
2g.21007404T>GCA345989937APOBc.9464A>C (p.Lys3155Thr)
c.5869+3329A>C (n.5869+3329A>C)
2g.21007404T=CA2493475235APOBc.9464A= (p.Lys3155=)
c.5869+3329A= (n.5869+3329A=)
2g.21007405T>ACA345989942APOBc.9463A>T (p.Lys3155Ter)
c.5869+3328A>T (n.5869+3328A>T)
2g.21007405T>CCA345989940APOBc.9463A>G (p.Lys3155Glu)
c.5869+3328A>G (n.5869+3328A>G)
2g.21007405T>GCA345989941APOBc.9463A>C (p.Lys3155Gln)
c.5869+3328A>C (n.5869+3328A>C)
2g.21007406T>ACA345989944APOBc.9462A>T (p.Glu3154Asp)
c.5869+3327A>T (n.5869+3327A>T)
2g.21007406T>CCA425344271APOBc.9462A>G (p.Glu3154=)
c.5869+3327A>G (n.5869+3327A>G)
dbSNP
2g.21007406T>GCA345989946APOBc.9462A>C (p.Glu3154Asp)
c.5869+3327A>C (n.5869+3327A>C)
2g.21007406T=CA2493475236APOBc.9462A= (p.Glu3154=)
c.5869+3327A= (n.5869+3327A=)
2g.21007407T>ACA345989949APOBc.9461A>T (p.Glu3154Val)
c.5869+3326A>T (n.5869+3326A>T)
2g.21007407T>CCA345989950APOBc.9461A>G (p.Glu3154Gly)
c.5869+3326A>G (n.5869+3326A>G)
2g.21007407T>GCA345989953APOBc.9461A>C (p.Glu3154Ala)
c.5869+3326A>C (n.5869+3326A>C)
2g.21007408C>ACA345989956APOBc.9460G>T (p.Glu3154Ter)
c.5869+3325G>T (n.5869+3325G>T)
2g.21007408C>GCA345989958APOBc.9460G>C (p.Glu3154Gln)
c.5869+3325G>C (n.5869+3325G>C)
2g.21007408C>TCA345989960APOBc.9460G>A (p.Glu3154Lys)
c.5869+3325G>A (n.5869+3325G>A)
gnomAD v4 COSMIC
2g.21007409C>ACA345989963APOBc.9459G>T (p.Trp3153Cys)
c.5869+3324G>T (n.5869+3324G>T)
2g.21007409C>GCA345989965APOBc.9459G>C (p.Trp3153Cys)
c.5869+3324G>C (n.5869+3324G>C)
2g.21007409C>TCA345989966APOBc.9459G>A (p.Trp3153Ter)
c.5869+3324G>A (n.5869+3324G>A)
COSMIC
2g.21007410C>ACA345989971APOBc.9458G>T (p.Trp3153Leu)
c.5869+3323G>T (n.5869+3323G>T)
2g.21007410C=CA2493475237APOBc.9458G= (p.Trp3153=)
c.5869+3323G= (n.5869+3323G=)
2g.21007410C>GCA345989973APOBc.9458G>C (p.Trp3153Ser)
c.5869+3323G>C (n.5869+3323G>C)
2g.21007410C>TCA345989969APOBc.9458G>A (p.Trp3153Ter)
c.5869+3323G>A (n.5869+3323G>A)
dbSNP gnomAD v3 gnomAD v4
2g.21007411A=CA2493475238APOBc.9457T= (p.Trp3153=)
c.5869+3322T= (n.5869+3322T=)
2g.21007411A>CCA345989979APOBc.9457T>G (p.Trp3153Gly)
c.5869+3322T>G (n.5869+3322T>G)
2g.21007411A>GCA345989976APOBc.9457T>C (p.Trp3153Arg)
c.5869+3322T>C (n.5869+3322T>C)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21007411A>TCA066556APOBc.9457T>A (p.Trp3153Arg)
c.5869+3322T>A (n.5869+3322T>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21007412T>ACA425344272APOBc.9456A>T (p.Leu3152=)
c.5869+3321A>T (n.5869+3321A>T)
2g.21007412T>CCA43497531APOBc.9456A>G (p.Leu3152=)
c.5869+3321A>G (n.5869+3321A>G)
dbSNP gnomAD v4
2g.21007412T>GCA425344273APOBc.9456A>C (p.Leu3152=)
c.5869+3321A>C (n.5869+3321A>C)
2g.21007412T=CA2493475239APOBc.9456A= (p.Leu3152=)
c.5869+3321A= (n.5869+3321A=)
2g.21007412_21007414delinsTAGCA2493475240APOBc.9454_9456delinsCTA (p.Leu3152=)
c.5869+3319_5869+3321delinsCTA (n.5869+3319_5869+3321delinsCTA)
2g.21007413A>CCA345989981APOBc.9455T>G (p.Leu3152Arg)
c.5869+3320T>G (n.5869+3320T>G)
2g.21007413A>GCA345989983APOBc.9455T>C (p.Leu3152Pro)
c.5869+3320T>C (n.5869+3320T>C)
gnomAD v4
2g.21007413A>TCA345989985APOBc.9455T>A (p.Leu3152Gln)
c.5869+3320T>A (n.5869+3320T>A)
2g.21007418_21007419delCA531312730APOBc.9454_9455del (p.Leu3152MetfsTer18)
c.5869+3319_5869+3320del (n.5869+3319_5869+3320del)
dbSNP gnomAD v2 gnomAD v4
2g.21007414G>ACA066552APOBc.9454C>T (p.Leu3152=)
c.5869+3319C>T (n.5869+3319C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21007414G>CCA066549APOBc.9454C>G (p.Leu3152Val)
c.5869+3319C>G (n.5869+3319C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21007414G=CA2493475241APOBc.9454C= (p.Leu3152=)
c.5869+3319C= (n.5869+3319C=)

Number of alleles fetched