Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21007303delCA2658076735APOBc.9566del (p.Pro3189LeufsTer28)
c.5869+3431del (n.5869+3431del)
gnomAD v4
2g.21007303G>ACA345989483APOBc.9565C>T (p.Pro3189Ser)
c.5869+3430C>T (n.5869+3430C>T)
COSMIC
2g.21007303G>CCA345989485APOBc.9565C>G (p.Pro3189Ala)
c.5869+3430C>G (n.5869+3430C>G)
2g.21007303G>TCA345989484APOBc.9565C>A (p.Pro3189Thr)
c.5869+3430C>A (n.5869+3430C>A)
2g.21007304A=CA2493475188APOBc.9564T= (p.Asn3188=)
c.5869+3429T= (n.5869+3429T=)
2g.21007304A>CCA345989486APOBc.9564T>G (p.Asn3188Lys)
c.5869+3429T>G (n.5869+3429T>G)
2g.21007304A>GCA425343869APOBc.9564T>C (p.Asn3188=)
c.5869+3429T>C (n.5869+3429T>C)
gnomAD v4
2g.21007304A>TCA345989487APOBc.9564T>A (p.Asn3188Lys)
c.5869+3429T>A (n.5869+3429T>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21007305T>ACA345989488APOBc.9563A>T (p.Asn3188Ile)
c.5869+3428A>T (n.5869+3428A>T)
2g.21007305T>CCA345989489APOBc.9563A>G (p.Asn3188Ser)
c.5869+3428A>G (n.5869+3428A>G)
gnomAD v4
2g.21007305T>GCA345989490APOBc.9563A>C (p.Asn3188Thr)
c.5869+3428A>C (n.5869+3428A>C)
2g.21007306T>ACA345989491APOBc.9562A>T (p.Asn3188Tyr)
c.5869+3427A>T (n.5869+3427A>T)
2g.21007306T>CCA345989492APOBc.9562A>G (p.Asn3188Asp)
c.5869+3427A>G (n.5869+3427A>G)
2g.21007306T>GCA345989493APOBc.9562A>C (p.Asn3188His)
c.5869+3427A>C (n.5869+3427A>C)
2g.21007307T>ACA425343878APOBc.9561A>T (p.Thr3187=)
c.5869+3426A>T (n.5869+3426A>T)
2g.21007307T>CCA425343880APOBc.9561A>G (p.Thr3187=)
c.5869+3426A>G (n.5869+3426A>G)
2g.21007307T>GCA425343881APOBc.9561A>C (p.Thr3187=)
c.5869+3426A>C (n.5869+3426A>C)
2g.21007308G>ACA345989494APOBc.9560C>T (p.Thr3187Ile)
c.5869+3425C>T (n.5869+3425C>T)
2g.21007308G>CCA345989495APOBc.9560C>G (p.Thr3187Arg)
c.5869+3425C>G (n.5869+3425C>G)
dbSNP COSMIC
2g.21007308G=CA2493475189APOBc.9560C= (p.Thr3187=)
c.5869+3425C= (n.5869+3425C=)
2g.21007308G>TCA345989496APOBc.9560C>A (p.Thr3187Lys)
c.5869+3425C>A (n.5869+3425C>A)
gnomAD v4
2g.21007309T>ACA345989497APOBc.9559A>T (p.Thr3187Ser)
c.5869+3424A>T (n.5869+3424A>T)
2g.21007309T>CCA345989499APOBc.9559A>G (p.Thr3187Ala)
c.5869+3424A>G (n.5869+3424A>G)
2g.21007309T>GCA345989498APOBc.9559A>C (p.Thr3187Pro)
c.5869+3424A>C (n.5869+3424A>C)
gnomAD v4
2g.21007310G>ACA425343886APOBc.9558C>T (p.Ile3186=)
c.5869+3423C>T (n.5869+3423C>T)
2g.21007310G>CCA345989500APOBc.9558C>G (p.Ile3186Met)
c.5869+3423C>G (n.5869+3423C>G)
2g.21007310G>TCA425343888APOBc.9558C>A (p.Ile3186=)
c.5869+3423C>A (n.5869+3423C>A)
2g.21007311A>CCA345989503APOBc.9557T>G (p.Ile3186Ser)
c.5869+3422T>G (n.5869+3422T>G)
2g.21007311A>GCA345989501APOBc.9557T>C (p.Ile3186Thr)
c.5869+3422T>C (n.5869+3422T>C)
2g.21007311A>TCA345989502APOBc.9557T>A (p.Ile3186Asn)
c.5869+3422T>A (n.5869+3422T>A)
2g.21007312T>ACA345989504APOBc.9556A>T (p.Ile3186Phe)
c.5869+3421A>T (n.5869+3421A>T)
2g.21007312T>CCA345989505APOBc.9556A>G (p.Ile3186Val)
c.5869+3421A>G (n.5869+3421A>G)
dbSNP gnomAD v2 gnomAD v4
2g.21007312T>GCA345989506APOBc.9556A>C (p.Ile3186Leu)
c.5869+3421A>C (n.5869+3421A>C)
2g.21007312T=CA2493475190APOBc.9556A= (p.Ile3186=)
c.5869+3421A= (n.5869+3421A=)
2g.21007313G>ACA43497196APOBc.9555C>T (p.Ser3185=)
c.5869+3420C>T (n.5869+3420C>T)
dbSNP
2g.21007313G>CCA425343893APOBc.9555C>G (p.Ser3185=)
c.5869+3420C>G (n.5869+3420C>G)
2g.21007313G=CA2493475191APOBc.9555C= (p.Ser3185=)
c.5869+3420C= (n.5869+3420C=)
2g.21007313G>TCA425343891APOBc.9555C>A (p.Ser3185=)
c.5869+3420C>A (n.5869+3420C>A)
2g.21007314G>ACA43497212APOBc.9554C>T (p.Ser3185Phe)
c.5869+3419C>T (n.5869+3419C>T)
dbSNP
2g.21007314G>CCA345989507APOBc.9554C>G (p.Ser3185Cys)
c.5869+3419C>G (n.5869+3419C>G)
2g.21007314G=CA2493475192APOBc.9554C= (p.Ser3185=)
c.5869+3419C= (n.5869+3419C=)
2g.21007314G>TCA345989508APOBc.9554C>A (p.Ser3185Tyr)
c.5869+3419C>A (n.5869+3419C>A)
gnomAD v4
2g.21007315A>CCA345989509APOBc.9553T>G (p.Ser3185Ala)
c.5869+3418T>G (n.5869+3418T>G)
2g.21007315A>GCA345989510APOBc.9553T>C (p.Ser3185Pro)
c.5869+3418T>C (n.5869+3418T>C)
2g.21007315A>TCA345989511APOBc.9553T>A (p.Ser3185Thr)
c.5869+3418T>A (n.5869+3418T>A)
2g.21007316A>CCA345989512APOBc.9552T>G (p.His3184Gln)
c.5869+3417T>G (n.5869+3417T>G)
2g.21007316A>GCA425343906APOBc.9552T>C (p.His3184=)
c.5869+3417T>C (n.5869+3417T>C)
2g.21007316A>TCA345989513APOBc.9552T>A (p.His3184Gln)
c.5869+3417T>A (n.5869+3417T>A)
2g.21007317T>ACA066667APOBc.9551A>T (p.His3184Leu)
c.5869+3416A>T (n.5869+3416A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21007317T>CCA345989515APOBc.9551A>G (p.His3184Arg)
c.5869+3416A>G (n.5869+3416A>G)

Number of alleles fetched