Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154966555T>A | CA414916572 | F8 | c.1142A>T (p.Asp381Val) c.*1018A>T (n.*1018A>T) c.1037A>T (p.Asp346Val) | |
X | g.154966555T>C | CA414916574 | F8 | c.1142A>G (p.Asp381Gly) c.*1018A>G (n.*1018A>G) c.1037A>G (p.Asp346Gly) | |
X | g.154966555T>G | CA414916582 | F8 | c.1142A>C (p.Asp381Ala) c.*1018A>C (n.*1018A>C) c.1037A>C (p.Asp346Ala) | |
X | g.154966556C>A | CA414916587 | F8 | c.1141G>T (p.Asp381Tyr) c.*1017G>T (n.*1017G>T) c.1036G>T (p.Asp346Tyr) | |
X | g.154966556C>G | CA414916592 | F8 | c.1141G>C (p.Asp381His) c.*1017G>C (n.*1017G>C) c.1036G>C (p.Asp346His) | |
X | g.154966556C>T | CA414916589 | F8 | c.1141G>A (p.Asp381Asn) c.*1017G>A (n.*1017G>A) c.1036G>A (p.Asp346Asn) | COSMIC COSMIC |
X | g.154966557A= | CA2466848127 | F8 | c.1140T= (p.Asp380=) c.*1016T= (n.*1016T=) c.1035T= (p.Asp345=) | |
X | g.154966557A>C | CA414916595 | F8 | c.1140T>G (p.Asp380Glu) c.*1016T>G (n.*1016T>G) c.1035T>G (p.Asp345Glu) | |
X | g.154966557A>G | CA519365243 | F8 | c.1140T>C (p.Asp380=) c.*1016T>C (n.*1016T>C) c.1035T>C (p.Asp345=) | dbSNP |
X | g.154966557A>T | CA414916598 | F8 | c.1140T>A (p.Asp380Glu) c.*1016T>A (n.*1016T>A) c.1035T>A (p.Asp345Glu) | |
X | g.154966558T>A | CA414916601 | F8 | c.1139A>T (p.Asp380Val) c.*1015A>T (n.*1015A>T) c.1034A>T (p.Asp345Val) | |
X | g.154966558T>C | CA10568496 | F8 | c.1139A>G (p.Asp380Gly) c.*1015A>G (n.*1015A>G) c.1034A>G (p.Asp345Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154966558T>G | CA414916606 | F8 | c.1139A>C (p.Asp380Ala) c.*1015A>C (n.*1015A>C) c.1034A>C (p.Asp345Ala) | |
X | g.154966558T= | CA2466848128 | F8 | c.1139A= (p.Asp380=) c.*1015A= (n.*1015A=) c.1034A= (p.Asp345=) | |
X | g.154966559C>A | CA414916609 | F8 | c.1138G>T (p.Asp380Tyr) c.*1014G>T (n.*1014G>T) c.1033G>T (p.Asp345Tyr) | |
X | g.154966559C= | CA2466848129 | F8 | c.1138G= (p.Asp380=) c.*1014G= (n.*1014G=) c.1033G= (p.Asp345=) | |
X | g.154966559C>G | CA414916615 | F8 | c.1138G>C (p.Asp380His) c.*1014G>C (n.*1014G>C) c.1033G>C (p.Asp345His) | |
X | g.154966559C>T | CA10568497 | F8 | c.1138G>A (p.Asp380Asn) c.*1014G>A (n.*1014G>A) c.1033G>A (p.Asp345Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154966561_154966572del | CA2695237371 | F8 | c.1127_1138del (p.Val376_Phe379del) c.*1003_*1014del (n.*1003_*1014del) c.1022_1033del (p.Val341_Phe344del) | |
X | g.154966560A= | CA2466848130 | F8 | c.1137T= (p.Phe379=) c.*1013T= (n.*1013T=) c.1032T= (p.Phe344=) | |
X | g.154966560A>C | CA414916618 | F8 | c.1137T>G (p.Phe379Leu) c.*1013T>G (n.*1013T>G) c.1032T>G (p.Phe344Leu) | |
X | g.154966560A>G | CA519365361 | F8 | c.1137T>C (p.Phe379=) c.*1013T>C (n.*1013T>C) c.1032T>C (p.Phe344=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154966560A>T | CA414916620 | F8 | c.1137T>A (p.Phe379Leu) c.*1013T>A (n.*1013T>A) c.1032T>A (p.Phe344Leu) | |
X | g.154966561A>C | CA414916624 | F8 | c.1136T>G (p.Phe379Cys) c.*1012T>G (n.*1012T>G) c.1031T>G (p.Phe344Cys) | gnomAD v4 |
X | g.154966561A>G | CA414916629 | F8 | c.1136T>C (p.Phe379Ser) c.*1012T>C (n.*1012T>C) c.1031T>C (p.Phe344Ser) | |
X | g.154966561A>T | CA414916626 | F8 | c.1136T>A (p.Phe379Tyr) c.*1012T>A (n.*1012T>A) c.1031T>A (p.Phe344Tyr) | |
X | g.154966562A>C | CA414916631 | F8 | c.1135T>G (p.Phe379Val) c.*1011T>G (n.*1011T>G) c.1030T>G (p.Phe344Val) | |
X | g.154966562A>G | CA414916634 | F8 | c.1135T>C (p.Phe379Leu) c.*1011T>C (n.*1011T>C) c.1030T>C (p.Phe344Leu) | |
X | g.154966562A>T | CA414916635 | F8 | c.1135T>A (p.Phe379Ile) c.*1011T>A (n.*1011T>A) c.1030T>A (p.Phe344Ile) | |
X | g.154966562_154966563delinsAC | CA2466848131 | F8 | c.1134_1135delinsGT (p.Arg378=) c.*1010_*1011delinsGT (n.*1010_*1011delinsGT) c.1029_1030delinsGT (p.Arg343=) | |
X | g.154966563C>A | CA10568499 | F8 | c.1134G>T (p.Arg378Ser) c.*1010G>T (n.*1010G>T) c.1029G>T (p.Arg343Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154966563C= | CA2466848132 | F8 | c.1134G= (p.Arg378=) c.*1010G= (n.*1010G=) c.1029G= (p.Arg343=) | |
X | g.154966563C>G | CA414916636 | F8 | c.1134G>C (p.Arg378Ser) c.*1010G>C (n.*1010G>C) c.1029G>C (p.Arg343Ser) | |
X | g.154966563C>T | CA10568498 | F8 | c.1134G>A (p.Arg378=) c.*1010G>A (n.*1010G>A) c.1029G>A (p.Arg343=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154966564del | CA873344580 | F8 | c.1134del (p.Arg378SerfsTer?) c.*1010del (n.*1010del) c.1029del (p.Arg343SerfsTer?) | dbSNP |
X | g.154966564C>A | CA414916639 | F8 | c.1133G>T (p.Arg378Met) c.*1009G>T (n.*1009G>T) c.1028G>T (p.Arg343Met) | |
X | g.154966564C>G | CA414916642 | F8 | c.1133G>C (p.Arg378Thr) c.*1009G>C (n.*1009G>C) c.1028G>C (p.Arg343Thr) | |
X | g.154966564C>T | CA414916646 | F8 | c.1133G>A (p.Arg378Lys) c.*1009G>A (n.*1009G>A) c.1028G>A (p.Arg343Lys) | gnomAD v4 |
X | g.154966565T>A | CA414916649 | F8 | c.1132A>T (p.Arg378Trp) c.*1008A>T (n.*1008A>T) c.1027A>T (p.Arg343Trp) | gnomAD v4 |
X | g.154966565T>C | CA414916651 | F8 | c.1132A>G (p.Arg378Gly) c.*1008A>G (n.*1008A>G) c.1027A>G (p.Arg343Gly) | |
X | g.154966565T>G | CA519365392 | F8 | c.1132A>C (p.Arg378=) c.*1008A>C (n.*1008A>C) c.1027A>C (p.Arg343=) | |
X | g.154966566G>A | CA519365396 | F8 | c.1131C>T (p.Val377=) c.*1007C>T (n.*1007C>T) c.1026C>T (p.Val342=) | |
X | g.154966566G>C | CA519365399 | F8 | c.1131C>G (p.Val377=) c.*1007C>G (n.*1007C>G) c.1026C>G (p.Val342=) | dbSNP |
X | g.154966566G= | CA2466848133 | F8 | c.1131C= (p.Val377=) c.*1007C= (n.*1007C=) c.1026C= (p.Val342=) | |
X | g.154966566G>T | CA519365402 | F8 | c.1131C>A (p.Val377=) c.*1007C>A (n.*1007C>A) c.1026C>A (p.Val342=) | |
X | g.154966567A>C | CA414916654 | F8 | c.1130T>G (p.Val377Gly) c.*1006T>G (n.*1006T>G) c.1025T>G (p.Val342Gly) | |
X | g.154966567A>G | CA414916660 | F8 | c.1130T>C (p.Val377Ala) c.*1006T>C (n.*1006T>C) c.1025T>C (p.Val342Ala) | |
X | g.154966567A>T | CA414916657 | F8 | c.1130T>A (p.Val377Asp) c.*1006T>A (n.*1006T>A) c.1025T>A (p.Val342Asp) | |
X | g.154966568C>A | CA414916662 | F8 | c.1129G>T (p.Val377Phe) c.*1005G>T (n.*1005G>T) c.1024G>T (p.Val342Phe) | |
X | g.154966568C>G | CA414916665 | F8 | c.1129G>C (p.Val377Leu) c.*1005G>C (n.*1005G>C) c.1024G>C (p.Val342Leu) |