Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154929999del | CA2695238170 | F8 | c.3791del (p.Ala1264ValfsTer10) c.3686del (p.Ala1229ValfsTer10) | |
X | g.154929999G>A | CA414894520 | F8 | c.3791C>T (p.Ala1264Val) c.3686C>T (p.Ala1229Val) | |
X | g.154929999G>C | CA414894523 | F8 | c.3791C>G (p.Ala1264Gly) c.3686C>G (p.Ala1229Gly) | |
X | g.154929999G>T | CA414894526 | F8 | c.3791C>A (p.Ala1264Asp) c.3686C>A (p.Ala1229Asp) | |
X | g.154930000C>A | CA414894528 | F8 | c.3790G>T (p.Ala1264Ser) c.3685G>T (p.Ala1229Ser) | |
X | g.154930000C>G | CA414894530 | F8 | c.3790G>C (p.Ala1264Pro) c.3685G>C (p.Ala1229Pro) | |
X | g.154930000C>T | CA414894533 | F8 | c.3790G>A (p.Ala1264Thr) c.3685G>A (p.Ala1229Thr) | |
X | g.154930001A>C | CA414894539 | F8 | c.3789T>G (p.Tyr1263Ter) c.3684T>G (p.Tyr1228Ter) | |
X | g.154930001A>G | CA519718823 | F8 | c.3789T>C (p.Tyr1263=) c.3684T>C (p.Tyr1228=) | |
X | g.154930001A>T | CA414894536 | F8 | c.3789T>A (p.Tyr1263Ter) c.3684T>A (p.Tyr1228Ter) | |
X | g.154930002T>A | CA414894542 | F8 | c.3788A>T (p.Tyr1263Phe) c.3683A>T (p.Tyr1228Phe) | |
X | g.154930002T>C | CA414894545 | F8 | c.3788A>G (p.Tyr1263Cys) c.3683A>G (p.Tyr1228Cys) | dbSNP |
X | g.154930002T>G | CA414894547 | F8 | c.3788A>C (p.Tyr1263Ser) c.3683A>C (p.Tyr1228Ser) | |
X | g.154930002T= | CA2466836204 | F8 | c.3788A= (p.Tyr1263=) c.3683A= (p.Tyr1228=) | |
X | g.154930003A= | CA2466836205 | F8 | c.3787T= (p.Tyr1263=) c.3682T= (p.Tyr1228=) | |
X | g.154930003A>C | CA414894550 | F8 | c.3787T>G (p.Tyr1263Asp) c.3682T>G (p.Tyr1228Asp) | |
X | g.154930003A>G | CA414894553 | F8 | c.3787T>C (p.Tyr1263His) c.3682T>C (p.Tyr1228His) | |
X | g.154930003A>T | CA337324880 | F8 | c.3787T>A (p.Tyr1263Asn) c.3682T>A (p.Tyr1228Asn) | dbSNP |
X | g.154930004T>A | CA519718827 | F8 | c.3786A>T (p.Ala1262=) c.3681A>T (p.Ala1227=) | |
X | g.154930004T>C | CA519718828 | F8 | c.3786A>G (p.Ala1262=) c.3681A>G (p.Ala1227=) | |
X | g.154930004T>G | CA519718829 | F8 | c.3786A>C (p.Ala1262=) c.3681A>C (p.Ala1227=) | |
X | g.154930005G>A | CA414894558 | F8 | c.3785C>T (p.Ala1262Val) c.3680C>T (p.Ala1227Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154930005G>C | CA414894564 | F8 | c.3785C>G (p.Ala1262Gly) c.3680C>G (p.Ala1227Gly) | |
X | g.154930005G= | CA2466836206 | F8 | c.3785C= (p.Ala1262=) c.3680C= (p.Ala1227=) | |
X | g.154930005G>T | CA414894561 | F8 | c.3785C>A (p.Ala1262Glu) c.3680C>A (p.Ala1227Glu) | COSMIC COSMIC |
X | g.154930006C>A | CA414894568 | F8 | c.3784G>T (p.Ala1262Ser) c.3679G>T (p.Ala1227Ser) | |
X | g.154930006C>G | CA414894577 | F8 | c.3784G>C (p.Ala1262Pro) c.3679G>C (p.Ala1227Pro) | gnomAD v4 |
X | g.154930006C>T | CA414894580 | F8 | c.3784G>A (p.Ala1262Thr) c.3679G>A (p.Ala1227Thr) | |
X | g.154930009dup | CA2824302383 | F8 | c.3784dup (p.Ala1262GlyfsTer10) c.3679dup (p.Ala1227GlyfsTer10) | |
X | g.154930007C>A | CA519718831 | F8 | c.3783G>T (p.Gly1261=) c.3678G>T (p.Gly1226=) | gnomAD v4 |
X | g.154930007C= | CA2466836207 | F8 | c.3783G= (p.Gly1261=) c.3678G= (p.Gly1226=) | |
X | g.154930007C>G | CA519718832 | F8 | c.3783G>C (p.Gly1261=) c.3678G>C (p.Gly1226=) | |
X | g.154930007C>T | CA10568178 | F8 | c.3783G>A (p.Gly1261=) c.3678G>A (p.Gly1226=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154930008C>A | CA414894586 | F8 | c.3782G>T (p.Gly1261Val) c.3677G>T (p.Gly1226Val) | |
X | g.154930008C>G | CA414894588 | F8 | c.3782G>C (p.Gly1261Ala) c.3677G>C (p.Gly1226Ala) | |
X | g.154930008C>T | CA414894591 | F8 | c.3782G>A (p.Gly1261Glu) c.3677G>A (p.Gly1226Glu) | COSMIC COSMIC |
X | g.154930009C>A | CA414894596 | F8 | c.3781G>T (p.Gly1261Trp) c.3676G>T (p.Gly1226Trp) | |
X | g.154930009C= | CA2466836208 | F8 | c.3781G= (p.Gly1261=) c.3676G= (p.Gly1226=) | |
X | g.154930009C>G | CA414894598 | F8 | c.3781G>C (p.Gly1261Arg) c.3676G>C (p.Gly1226Arg) | |
X | g.154930009C>T | CA10568179 | F8 | c.3781G>A (p.Gly1261Arg) c.3676G>A (p.Gly1226Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154930010del | CA2499226518 | F8 | c.3780del (p.Asp1260GlufsTer14) c.3675del (p.Asp1225GlufsTer14) | ClinVar dbSNP |
X | g.154930010G>A | CA10568180 | F8 | c.3780C>T (p.Asp1260=) c.3675C>T (p.Asp1225=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154930010G>C | CA343865 | F8 | c.3780C>G (p.Asp1260Glu) c.3675C>G (p.Asp1225Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154930010G= | CA2466836209 | F8 | c.3780C= (p.Asp1260=) c.3675C= (p.Asp1225=) | |
X | g.154930010G>T | CA10568181 | F8 | c.3780C>A (p.Asp1260Glu) c.3675C>A (p.Asp1225Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154930011T>A | CA10568182 | F8 | c.3779A>T (p.Asp1260Val) c.3674A>T (p.Asp1225Val) | dbSNP ExAC |
X | g.154930011T>C | CA414894620 | F8 | c.3779A>G (p.Asp1260Gly) c.3674A>G (p.Asp1225Gly) | |
X | g.154930011T>G | CA414894616 | F8 | c.3779A>C (p.Asp1260Ala) c.3674A>C (p.Asp1225Ala) | |
X | g.154930011T= | CA2466836210 | F8 | c.3779A= (p.Asp1260=) c.3674A= (p.Asp1225=) | |
X | g.154930012C>A | CA414894622 | F8 | c.3778G>T (p.Asp1260Tyr) c.3673G>T (p.Asp1225Tyr) |