Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21002407_21002416delCA2658054429APOBc.13008_13017del (p.Phe4337IlefsTer9)
c.13008_13017del (p.Phe4337IlefsTer?)
c.5870-3141_5870-3132del (n.5870-3141_5870-3132del)
gnomAD v4
2g.21002409C>ACA345969827APOBc.13013G>T (p.Ser4338Ile)
c.5870-3136G>T (n.5870-3136G>T)
2g.21002409C=CA2493472970APOBc.13013G= (p.Ser4338=)
c.5870-3136G= (n.5870-3136G=)
2g.21002409C>GCA345969825APOBc.13013G>C (p.Ser4338Thr)
c.5870-3136G>C (n.5870-3136G>C)
gnomAD v4
2g.21002409C>TCA022788APOBc.13013G>A (p.Ser4338Asn)
c.5870-3136G>A (n.5870-3136G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002409_21002411delinsCTGCA2493472971APOBc.13011_13013delinsCAG (p.Phe4337=)
c.5870-3138_5870-3136delinsCAG (n.5870-3138_5870-3136delinsCAG)
2g.21002409_21002411delinsTTTCA1139655568APOBc.13011_13013delinsAAA (p.Phe4337_Ser4338delinsLeuAsn)
c.5870-3138_5870-3136delinsAAA (n.5870-3138_5870-3136delinsAAA)
ClinVar dbSNP
2g.21002410T>ACA345969829APOBc.13012A>T (p.Ser4338Cys)
c.5870-3137A>T (n.5870-3137A>T)
2g.21002410T>CCA345969830APOBc.13012A>G (p.Ser4338Gly)
c.5870-3137A>G (n.5870-3137A>G)
2g.21002410T>GCA345969832APOBc.13012A>C (p.Ser4338Arg)
c.5870-3137A>C (n.5870-3137A>C)
2g.21002411G>ACA425341960APOBc.13011C>T (p.Phe4337=)
c.5870-3138C>T (n.5870-3138C>T)
ClinVar dbSNP gnomAD v4
2g.21002411G>CCA345969835APOBc.13011C>G (p.Phe4337Leu)
c.5870-3138C>G (n.5870-3138C>G)
2g.21002411G>TCA345969836APOBc.13011C>A (p.Phe4337Leu)
c.5870-3138C>A (n.5870-3138C>A)
gnomAD v4
2g.21002412A>CCA345969837APOBc.13010T>G (p.Phe4337Cys)
c.5870-3139T>G (n.5870-3139T>G)
2g.21002412A>GCA345969839APOBc.13010T>C (p.Phe4337Ser)
c.5870-3139T>C (n.5870-3139T>C)
2g.21002412A>TCA345969841APOBc.13010T>A (p.Phe4337Tyr)
c.5870-3139T>A (n.5870-3139T>A)
2g.21002413A>CCA345969843APOBc.13009T>G (p.Phe4337Val)
c.5870-3140T>G (n.5870-3140T>G)
2g.21002413A>GCA345969844APOBc.13009T>C (p.Phe4337Leu)
c.5870-3140T>C (n.5870-3140T>C)
gnomAD v4
2g.21002413A>TCA345969846APOBc.13009T>A (p.Phe4337Ile)
c.5870-3140T>A (n.5870-3140T>A)
2g.21002414G>ACA43488271APOBc.13008C>T (p.Ile4336=)
c.5870-3141C>T (n.5870-3141C>T)
dbSNP
2g.21002414G>CCA345969849APOBc.13008C>G (p.Ile4336Met)
c.5870-3141C>G (n.5870-3141C>G)
2g.21002414G=CA2493472972APOBc.13008C= (p.Ile4336=)
c.5870-3141C= (n.5870-3141C=)
2g.21002414G>TCA425341965APOBc.13008C>A (p.Ile4336=)
c.5870-3141C>A (n.5870-3141C>A)
gnomAD v4
2g.21002415A>CCA345969853APOBc.13007T>G (p.Ile4336Ser)
c.5870-3142T>G (n.5870-3142T>G)
2g.21002415A>GCA345969850APOBc.13007T>C (p.Ile4336Thr)
c.5870-3142T>C (n.5870-3142T>C)
2g.21002415A>TCA345969852APOBc.13007T>A (p.Ile4336Asn)
c.5870-3142T>A (n.5870-3142T>A)
2g.21002416T>ACA345969855APOBc.13006A>T (p.Ile4336Phe)
c.5870-3143A>T (n.5870-3143A>T)
2g.21002416T>CCA345969857APOBc.13006A>G (p.Ile4336Val)
c.5870-3143A>G (n.5870-3143A>G)
gnomAD v4
2g.21002416T>GCA345969859APOBc.13006A>C (p.Ile4336Leu)
c.5870-3143A>C (n.5870-3143A>C)
2g.21002417T>ACA425341972APOBc.13005A>T (p.Thr4335=)
c.5870-3144A>T (n.5870-3144A>T)
dbSNP gnomAD v2 gnomAD v4
2g.21002417T>CCA425341974APOBc.13005A>G (p.Thr4335=)
c.5870-3144A>G (n.5870-3144A>G)
2g.21002417T>GCA425341975APOBc.13005A>C (p.Thr4335=)
c.5870-3144A>C (n.5870-3144A>C)
2g.21002417T=CA2493472973APOBc.13005A= (p.Thr4335=)
c.5870-3144A= (n.5870-3144A=)
2g.21002418G>ACA345969861APOBc.13004C>T (p.Thr4335Ile)
c.5870-3145C>T (n.5870-3145C>T)
ClinVar dbSNP
2g.21002418G>CCA345969863APOBc.13004C>G (p.Thr4335Arg)
c.5870-3145C>G (n.5870-3145C>G)
2g.21002418G=CA2493472974APOBc.13004C= (p.Thr4335=)
c.5870-3145C= (n.5870-3145C=)
2g.21002418G>TCA345969865APOBc.13004C>A (p.Thr4335Lys)
c.5870-3145C>A (n.5870-3145C>A)
2g.21002419T>ACA345969867APOBc.13003A>T (p.Thr4335Ser)
c.5870-3146A>T (n.5870-3146A>T)
2g.21002419T>CCA345969869APOBc.13003A>G (p.Thr4335Ala)
c.5870-3146A>G (n.5870-3146A>G)
ClinVar dbSNP gnomAD v4
2g.21002419T>GCA345969870APOBc.13003A>C (p.Thr4335Pro)
c.5870-3146A>C (n.5870-3146A>C)
2g.21002419T=CA2493472975APOBc.13003A= (p.Thr4335=)
c.5870-3146A= (n.5870-3146A=)
2g.21002420G>ACA425341980APOBc.13002C>T (p.Asn4334=)
c.5870-3147C>T (n.5870-3147C>T)
dbSNP gnomAD v4
2g.21002420G>CCA345969873APOBc.13002C>G (p.Asn4334Lys)
c.5870-3147C>G (n.5870-3147C>G)
2g.21002420G=CA2493472976APOBc.13002C= (p.Asn4334=)
c.5870-3147C= (n.5870-3147C=)
2g.21002420G>TCA345969875APOBc.13002C>A (p.Asn4334Lys)
c.5870-3147C>A (n.5870-3147C>A)
2g.21002421T>ACA345969881APOBc.13001A>T (p.Asn4334Ile)
c.5870-3148A>T (n.5870-3148A>T)
2g.21002421T>CCA345969879APOBc.13001A>G (p.Asn4334Ser)
c.5870-3148A>G (n.5870-3148A>G)
2g.21002421T>GCA345969877APOBc.13001A>C (p.Asn4334Thr)
c.5870-3148A>C (n.5870-3148A>C)
2g.21002422T>ACA345969883APOBc.13000A>T (p.Asn4334Tyr)
c.5870-3149A>T (n.5870-3149A>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002422T>CCA345969887APOBc.13000A>G (p.Asn4334Asp)
c.5870-3149A>G (n.5870-3149A>G)

Number of alleles fetched