Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.21007392T>A | CA345989882 | APOB | c.9476A>T (p.Lys3159Met) c.5869+3341A>T (n.5869+3341A>T) | |
2 | g.21007392T>C | CA345989884 | APOB | c.9476A>G (p.Lys3159Arg) c.5869+3341A>G (n.5869+3341A>G) | |
2 | g.21007392T>G | CA345989886 | APOB | c.9476A>C (p.Lys3159Thr) c.5869+3341A>C (n.5869+3341A>C) | |
2 | g.21007393T>A | CA345989890 | APOB | c.9475A>T (p.Lys3159Ter) c.5869+3340A>T (n.5869+3340A>T) | |
2 | g.21007393T>C | CA345989893 | APOB | c.9475A>G (p.Lys3159Glu) c.5869+3340A>G (n.5869+3340A>G) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.21007393T>G | CA345989891 | APOB | c.9475A>C (p.Lys3159Gln) c.5869+3340A>C (n.5869+3340A>C) | |
2 | g.21007393T= | CA2493475228 | APOB | c.9475A= (p.Lys3159=) c.5869+3340A= (n.5869+3340A=) | |
2 | g.21007394C>A | CA345989896 | APOB | c.9474G>T (p.Leu3158Phe) c.5869+3339G>T (n.5869+3339G>T) | |
2 | g.21007394C>G | CA345989897 | APOB | c.9474G>C (p.Leu3158Phe) c.5869+3339G>C (n.5869+3339G>C) | COSMIC |
2 | g.21007394C>T | CA425344257 | APOB | c.9474G>A (p.Leu3158=) c.5869+3339G>A (n.5869+3339G>A) | |
2 | g.21007395A= | CA2493475229 | APOB | c.9473T= (p.Leu3158=) c.5869+3338T= (n.5869+3338T=) | |
2 | g.21007395A>C | CA345989900 | APOB | c.9473T>G (p.Leu3158Trp) c.5869+3338T>G (n.5869+3338T>G) | |
2 | g.21007395A>G | CA066574 | APOB | c.9473T>C (p.Leu3158Ser) c.5869+3338T>C (n.5869+3338T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.21007395A>T | CA345989903 | APOB | c.9473T>A (p.Leu3158Ter) c.5869+3338T>A (n.5869+3338T>A) | |
2 | g.21007396A>C | CA345989906 | APOB | c.9472T>G (p.Leu3158Val) c.5869+3337T>G (n.5869+3337T>G) | |
2 | g.21007396A>G | CA425344259 | APOB | c.9472T>C (p.Leu3158=) c.5869+3337T>C (n.5869+3337T>C) | |
2 | g.21007396A>T | CA345989908 | APOB | c.9472T>A (p.Leu3158Met) c.5869+3337T>A (n.5869+3337T>A) | |
2 | g.21007397G>A | CA066572 | APOB | c.9471C>T (p.Gly3157=) c.5869+3336C>T (n.5869+3336C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.21007397G>C | CA425344263 | APOB | c.9471C>G (p.Gly3157=) c.5869+3336C>G (n.5869+3336C>G) | |
2 | g.21007397G= | CA2493475230 | APOB | c.9471C= (p.Gly3157=) c.5869+3336C= (n.5869+3336C=) | |
2 | g.21007397G>T | CA425344261 | APOB | c.9471C>A (p.Gly3157=) c.5869+3336C>A (n.5869+3336C>A) | COSMIC |
2 | g.21007398C>A | CA345989911 | APOB | c.9470G>T (p.Gly3157Val) c.5869+3335G>T (n.5869+3335G>T) | dbSNP |
2 | g.21007398C= | CA2493475231 | APOB | c.9470G= (p.Gly3157=) c.5869+3335G= (n.5869+3335G=) | |
2 | g.21007398C>G | CA345989912 | APOB | c.9470G>C (p.Gly3157Ala) c.5869+3335G>C (n.5869+3335G>C) | ClinVar dbSNP |
2 | g.21007398C>T | CA066569 | APOB | c.9470G>A (p.Gly3157Asp) c.5869+3335G>A (n.5869+3335G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.21007399C>A | CA345989915 | APOB | c.9469G>T (p.Gly3157Cys) c.5869+3334G>T (n.5869+3334G>T) | |
2 | g.21007399C= | CA2493475232 | APOB | c.9469G= (p.Gly3157=) c.5869+3334G= (n.5869+3334G=) | |
2 | g.21007399C>G | CA066567 | APOB | c.9469G>C (p.Gly3157Arg) c.5869+3334G>C (n.5869+3334G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.21007399C>T | CA345989917 | APOB | c.9469G>A (p.Gly3157Ser) c.5869+3334G>A (n.5869+3334G>A) | COSMIC |
2 | g.21007400T>A | CA425344268 | APOB | c.9468A>T (p.Thr3156=) c.5869+3333A>T (n.5869+3333A>T) | |
2 | g.21007400T>C | CA425344267 | APOB | c.9468A>G (p.Thr3156=) c.5869+3333A>G (n.5869+3333A>G) | |
2 | g.21007400T>G | CA425344266 | APOB | c.9468A>C (p.Thr3156=) c.5869+3333A>C (n.5869+3333A>C) | gnomAD v4 |
2 | g.21007401G>A | CA066564 | APOB | c.9467C>T (p.Thr3156Ile) c.5869+3332C>T (n.5869+3332C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.21007401G>C | CA345989921 | APOB | c.9467C>G (p.Thr3156Arg) c.5869+3332C>G (n.5869+3332C>G) | |
2 | g.21007401G= | CA2493475233 | APOB | c.9467C= (p.Thr3156=) c.5869+3332C= (n.5869+3332C=) | |
2 | g.21007401G>T | CA066560 | APOB | c.9467C>A (p.Thr3156Lys) c.5869+3332C>A (n.5869+3332C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.21007402T>A | CA345989924 | APOB | c.9466A>T (p.Thr3156Ser) c.5869+3331A>T (n.5869+3331A>T) | |
2 | g.21007402T>C | CA345989926 | APOB | c.9466A>G (p.Thr3156Ala) c.5869+3331A>G (n.5869+3331A>G) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.21007402T>G | CA345989927 | APOB | c.9466A>C (p.Thr3156Pro) c.5869+3331A>C (n.5869+3331A>C) | |
2 | g.21007402T= | CA2493475234 | APOB | c.9466A= (p.Thr3156=) c.5869+3331A= (n.5869+3331A=) | |
2 | g.21007407dup | CA531312729 | APOB | c.9466dup (p.Thr3156AsnfsTer15) c.5869+3331dup (n.5869+3331dup) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.21007407del | CA2658076738 | APOB | c.9466del (p.Thr3156GlnfsTer3) c.5869+3331del (n.5869+3331del) | gnomAD v4 |
2 | g.21007402_21007403insA | CA425344270 | APOB | c.9465_9466insT (p.Thr3156TyrfsTer15) c.5869+3330_5869+3331insT (n.5869+3330_5869+3331insT) | |
2 | g.21007403T>A | CA345989930 | APOB | c.9465A>T (p.Lys3155Asn) c.5869+3330A>T (n.5869+3330A>T) | |
2 | g.21007403T>C | CA425344269 | APOB | c.9465A>G (p.Lys3155=) c.5869+3330A>G (n.5869+3330A>G) | COSMIC |
2 | g.21007403T>G | CA345989932 | APOB | c.9465A>C (p.Lys3155Asn) c.5869+3330A>C (n.5869+3330A>C) | |
2 | g.21007404T>A | CA345989934 | APOB | c.9464A>T (p.Lys3155Ile) c.5869+3329A>T (n.5869+3329A>T) | |
2 | g.21007404T>C | CA066558 | APOB | c.9464A>G (p.Lys3155Arg) c.5869+3329A>G (n.5869+3329A>G) | dbSNP ExAC |
2 | g.21007404T>G | CA345989937 | APOB | c.9464A>C (p.Lys3155Thr) c.5869+3329A>C (n.5869+3329A>C) | |
2 | g.21007404T= | CA2493475235 | APOB | c.9464A= (p.Lys3155=) c.5869+3329A= (n.5869+3329A=) |