| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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.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) | |
| X | g.154966568C>T | CA414916667 | F8 | c.1129G>A (p.Val377Ile) c.*1005G>A (n.*1005G>A) c.1024G>A (p.Val342Ile) | |
| X | g.154966569C>A | CA519365405 | F8 | c.1128G>T (p.Val376=) c.*1004G>T (n.*1004G>T) c.1023G>T (p.Val341=) | |
| X | g.154966569C>G | CA519365409 | F8 | c.1128G>C (p.Val376=) c.*1004G>C (n.*1004G>C) c.1023G>C (p.Val341=) | |
| X | g.154966569C>T | CA519365410 | F8 | c.1128G>A (p.Val376=) c.*1004G>A (n.*1004G>A) c.1023G>A (p.Val341=) | |
| X | g.154966570A>C | CA414916672 | F8 | c.1127T>G (p.Val376Gly) c.*1003T>G (n.*1003T>G) c.1022T>G (p.Val341Gly) | |
| X | g.154966570A>G | CA414916674 | F8 | c.1127T>C (p.Val376Ala) c.*1003T>C (n.*1003T>C) c.1022T>C (p.Val341Ala) | |
| X | g.154966570A>T | CA414916677 | F8 | c.1127T>A (p.Val376Glu) c.*1003T>A (n.*1003T>A) c.1022T>A (p.Val341Glu) | |
| X | g.154966571del | CA2695237373 | F8 | c.1126del (p.Val376TrpfsTer?) c.*1002del (n.*1002del) c.1021del (p.Val341TrpfsTer?) | |
| X | g.154966571C>A | CA414916678 | F8 | c.1126G>T (p.Val376Leu) c.*1002G>T (n.*1002G>T) c.1021G>T (p.Val341Leu) | COSMIC COSMIC |
| X | g.154966571C= | CA2466848134 | F8 | c.1126G= (p.Val376=) c.*1002G= (n.*1002G=) c.1021G= (p.Val341=) | |
| X | g.154966571C>G | CA414916679 | F8 | c.1126G>C (p.Val376Leu) c.*1002G>C (n.*1002G>C) c.1021G>C (p.Val341Leu) | |
| X | g.154966571C>T | CA414916680 | F8 | c.1126G>A (p.Val376Met) c.*1002G>A (n.*1002G>A) c.1021G>A (p.Val341Met) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.154966572A>C | CA414916683 | F8 | c.1125T>G (p.Asp375Glu) c.*1001T>G (n.*1001T>G) c.1020T>G (p.Asp340Glu) | |
| X | g.154966572A>G | CA519365424 | F8 | c.1125T>C (p.Asp375=) c.*1001T>C (n.*1001T>C) c.1020T>C (p.Asp340=) | |
| X | g.154966572A>T | CA414916682 | F8 | c.1125T>A (p.Asp375Glu) c.*1001T>A (n.*1001T>A) c.1020T>A (p.Asp340Glu) | |
| X | g.154966573T>A | CA414916687 | F8 | c.1124A>T (p.Asp375Val) c.*1000A>T (n.*1000A>T) c.1019A>T (p.Asp340Val) | |
| X | g.154966573T>C | CA414916692 | F8 | c.1124A>G (p.Asp375Gly) c.*1000A>G (n.*1000A>G) c.1019A>G (p.Asp340Gly) | |
| X | g.154966573T>G | CA414916690 | F8 | c.1124A>C (p.Asp375Ala) c.*1000A>C (n.*1000A>C) c.1019A>C (p.Asp340Ala) | |
| X | g.154966574C>A | CA414916696 | F8 | c.1123G>T (p.Asp375Tyr) c.*999G>T (n.*999G>T) c.1018G>T (p.Asp340Tyr) | |
| X | g.154966574C>G | CA414916700 | F8 | c.1123G>C (p.Asp375His) c.*999G>C (n.*999G>C) c.1018G>C (p.Asp340His) | gnomAD v4 |
| X | g.154966574C>T | CA414916702 | F8 | c.1123G>A (p.Asp375Asn) c.*999G>A (n.*999G>A) c.1018G>A (p.Asp340Asn) | gnomAD v4 |
| X | g.154966575C>A | CA414916704 | F8 | c.1122G>T (p.Met374Ile) c.*998G>T (n.*998G>T) c.1017G>T (p.Met339Ile) | |
| X | g.154966575C= | CA2466848135 | F8 | c.1122G= (p.Met374=) c.*998G= (n.*998G=) c.1017G= (p.Met339=) | |
| X | g.154966575C>G | CA414916707 | F8 | c.1122G>C (p.Met374Ile) c.*998G>C (n.*998G>C) c.1017G>C (p.Met339Ile) | dbSNP |
| X | g.154966575C>T | CA414916712 | F8 | c.1122G>A (p.Met374Ile) c.*998G>A (n.*998G>A) c.1017G>A (p.Met339Ile) | |
| X | g.154966576A>C | CA414916715 | F8 | c.1121T>G (p.Met374Arg) c.*997T>G (n.*997T>G) c.1016T>G (p.Met339Arg) | |
| X | g.154966576A>G | CA414916717 | F8 | c.1121T>C (p.Met374Thr) c.*997T>C (n.*997T>C) c.1016T>C (p.Met339Thr) | |
| X | g.154966576A>T | CA414916720 | F8 | c.1121T>A (p.Met374Lys) c.*997T>A (n.*997T>A) c.1016T>A (p.Met339Lys) | |
| X | g.154966577T>A | CA414916722 | F8 | c.1120A>T (p.Met374Leu) c.*996A>T (n.*996A>T) c.1015A>T (p.Met339Leu) | |
| X | g.154966577T>C | CA414916724 | F8 | c.1120A>G (p.Met374Val) c.*996A>G (n.*996A>G) c.1015A>G (p.Met339Val) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.154966577T>G | CA414916727 | F8 | c.1120A>C (p.Met374Leu) c.*996A>C (n.*996A>C) c.1015A>C (p.Met339Leu) | |
| X | g.154966579del | CA2695197149 | F8 | c.1120del (p.Met374TrpfsTer?) c.*996del (n.*996del) c.1015del (p.Met339TrpfsTer?) | |
| X | g.154966578T>A | CA414916730 | F8 | c.1119A>T (p.Glu373Asp) c.*995A>T (n.*995A>T) c.1014A>T (p.Glu338Asp) |