| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154969468T>A | CA414918127 | F8 | c.872A>T (p.Glu291Val) c.*748A>T (n.*748A>T) c.767A>T (p.Glu256Val) | |
| X | g.154969468T>C | CA255017 | F8 | c.872A>G (p.Glu291Gly) c.*748A>G (n.*748A>G) c.767A>G (p.Glu256Gly) | ClinVar dbSNP |
| X | g.154969468T>G | CA414918129 | F8 | c.872A>C (p.Glu291Ala) c.*748A>C (n.*748A>C) c.767A>C (p.Glu256Ala) | |
| X | g.154969468T= | CA2466849027 | F8 | c.872A= (p.Glu291=) c.*748A= (n.*748A=) c.767A= (p.Glu256=) | |
| X | g.154969469del | CA2695237468 | F8 | c.871del (p.Glu291LysfsTer7) c.*747del (n.*747del) c.766del (p.Glu256LysfsTer7) | |
| X | g.154969469C>A | CA414918132 | F8 | c.871G>T (p.Glu291Ter) c.*747G>T (n.*747G>T) c.766G>T (p.Glu256Ter) | |
| X | g.154969469C= | CA2466849028 | F8 | c.871G= (p.Glu291=) c.*747G= (n.*747G=) c.766G= (p.Glu256=) | |
| X | g.154969469C>G | CA414918133 | F8 | c.871G>C (p.Glu291Gln) c.*747G>C (n.*747G>C) c.766G>C (p.Glu256Gln) | |
| X | g.154969469C>T | CA414918134 | F8 | c.871G>A (p.Glu291Lys) c.*747G>A (n.*747G>A) c.766G>A (p.Glu256Lys) | ClinVar dbSNP gnomAD v4 |
| X | g.154969470G>A | CA337337622 | F8 | c.870C>T (p.Leu290=) c.*746C>T (n.*746C>T) c.765C>T (p.Leu255=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.154969470G>C | CA519367521 | F8 | c.870C>G (p.Leu290=) c.*746C>G (n.*746C>G) c.765C>G (p.Leu255=) | |
| X | g.154969470G= | CA2466849029 | F8 | c.870C= (p.Leu290=) c.*746C= (n.*746C=) c.765C= (p.Leu255=) | |
| X | g.154969470G>T | CA519367524 | F8 | c.870C>A (p.Leu290=) c.*746C>A (n.*746C>A) c.765C>A (p.Leu255=) | |
| X | g.154969471A= | CA2466849030 | F8 | c.869T= (p.Leu290=) c.*745T= (n.*745T=) c.764T= (p.Leu255=) | |
| X | g.154969471A>C | CA414918137 | F8 | c.869T>G (p.Leu290Arg) c.*745T>G (n.*745T>G) c.764T>G (p.Leu255Arg) | |
| X | g.154969471A>G | CA414918139 | F8 | c.869T>C (p.Leu290Pro) c.*745T>C (n.*745T>C) c.764T>C (p.Leu255Pro) | dbSNP |
| X | g.154969471A>T | CA414918138 | F8 | c.869T>A (p.Leu290His) c.*745T>A (n.*745T>A) c.764T>A (p.Leu255His) | |
| X | g.154969472G>A | CA414918141 | F8 | c.868C>T (p.Leu290Phe) c.*744C>T (n.*744C>T) c.763C>T (p.Leu255Phe) | |
| X | g.154969472G>C | CA414918143 | F8 | c.868C>G (p.Leu290Val) c.*744C>G (n.*744C>G) c.763C>G (p.Leu255Val) | |
| X | g.154969472G>T | CA414918144 | F8 | c.868C>A (p.Leu290Ile) c.*744C>A (n.*744C>A) c.763C>A (p.Leu255Ile) | COSMIC COSMIC |
| X | g.154969473G>A | CA337337638 | F8 | c.867C>T (p.Phe289=) c.*743C>T (n.*743C>T) c.762C>T (p.Phe254=) | dbSNP gnomAD v4 |
| X | g.154969473G>C | CA414918145 | F8 | c.867C>G (p.Phe289Leu) c.*743C>G (n.*743C>G) c.762C>G (p.Phe254Leu) | |
| X | g.154969473G= | CA2466849031 | F8 | c.867C= (p.Phe289=) c.*743C= (n.*743C=) c.762C= (p.Phe254=) | |
| X | g.154969473G>T | CA414918147 | F8 | c.867C>A (p.Phe289Leu) c.*743C>A (n.*743C>A) c.762C>A (p.Phe254Leu) | |
| X | g.154969474A>C | CA414918150 | F8 | c.866T>G (p.Phe289Cys) c.*742T>G (n.*742T>G) c.761T>G (p.Phe254Cys) | |
| X | g.154969474A>G | CA414918151 | F8 | c.866T>C (p.Phe289Ser) c.*742T>C (n.*742T>C) c.761T>C (p.Phe254Ser) | |
| X | g.154969474A>T | CA414918152 | F8 | c.866T>A (p.Phe289Tyr) c.*742T>A (n.*742T>A) c.761T>A (p.Phe254Tyr) | |
| X | g.154969475A>C | CA414918157 | F8 | c.865T>G (p.Phe289Val) c.*741T>G (n.*741T>G) c.760T>G (p.Phe254Val) | |
| X | g.154969475A>G | CA414918155 | F8 | c.865T>C (p.Phe289Leu) c.*741T>C (n.*741T>C) c.760T>C (p.Phe254Leu) | |
| X | g.154969475A>T | CA414918153 | F8 | c.865T>A (p.Phe289Ile) c.*741T>A (n.*741T>A) c.760T>A (p.Phe254Ile) | |
| X | g.154969476T>A | CA519367536 | F8 | c.864A>T (p.Ile288=) c.*740A>T (n.*740A>T) c.759A>T (p.Ile253=) | |
| X | g.154969476T>C | CA414918159 | F8 | c.864A>G (p.Ile288Met) c.*740A>G (n.*740A>G) c.759A>G (p.Ile253Met) | |
| X | g.154969476T>G | CA519367538 | F8 | c.864A>C (p.Ile288=) c.*740A>C (n.*740A>C) c.759A>C (p.Ile253=) | |
| X | g.154969477A>C | CA414918165 | F8 | c.863T>G (p.Ile288Arg) c.*739T>G (n.*739T>G) c.758T>G (p.Ile253Arg) | |
| X | g.154969477A>G | CA414918161 | F8 | c.863T>C (p.Ile288Thr) c.*739T>C (n.*739T>C) c.758T>C (p.Ile253Thr) | |
| X | g.154969477A>T | CA414918163 | F8 | c.863T>A (p.Ile288Lys) c.*739T>A (n.*739T>A) c.758T>A (p.Ile253Lys) | |
| X | g.154969478T>A | CA414918167 | F8 | c.862A>T (p.Ile288Leu) c.*738A>T (n.*738A>T) c.757A>T (p.Ile253Leu) | |
| X | g.154969478T>C | CA414918170 | F8 | c.862A>G (p.Ile288Val) c.*738A>G (n.*738A>G) c.757A>G (p.Ile253Val) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.154969478T>G | CA414918172 | F8 | c.862A>C (p.Ile288Leu) c.*738A>C (n.*738A>C) c.757A>C (p.Ile253Leu) | |
| X | g.154969478T= | CA2466849032 | F8 | c.862A= (p.Ile288=) c.*738A= (n.*738A=) c.757A= (p.Ile253=) | |
| X | g.154969479del | CA2695237470 | F8 | c.862del (p.Ile288TyrfsTer10) c.*738del (n.*738del) c.757del (p.Ile253TyrfsTer10) | |
| X | g.154969479T>A | CA519367547 | F8 | c.861A>T (p.Ser287=) c.*737A>T (n.*737A>T) c.756A>T (p.Ser252=) | |
| X | g.154969479T>C | CA519367549 | F8 | c.861A>G (p.Ser287=) c.*737A>G (n.*737A>G) c.756A>G (p.Ser252=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.154969479T>G | CA519367551 | F8 | c.861A>C (p.Ser287=) c.*737A>C (n.*737A>C) c.756A>C (p.Ser252=) | |
| X | g.154969479T= | CA2466849033 | F8 | c.861A= (p.Ser287=) c.*737A= (n.*737A=) c.756A= (p.Ser252=) | |
| X | g.154969480G>A | CA414918174 | F8 | c.860C>T (p.Ser287Leu) c.*736C>T (n.*736C>T) c.755C>T (p.Ser252Leu) | |
| X | g.154969480G>C | CA414918176 | F8 | c.860C>G (p.Ser287Ter) c.*736C>G (n.*736C>G) c.755C>G (p.Ser252Ter) | dbSNP |
| X | g.154969480G= | CA2466849034 | F8 | c.860C= (p.Ser287=) c.*736C= (n.*736C=) c.755C= (p.Ser252=) | |
| X | g.154969480G>T | CA414918178 | F8 | c.860C>A (p.Ser287Ter) c.*736C>A (n.*736C>A) c.755C>A (p.Ser252Ter) | dbSNP |
| X | g.154969481A>C | CA414918180 | F8 | c.859T>G (p.Ser287Ala) c.*735T>G (n.*735T>G) c.754T>G (p.Ser252Ala) |