Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154969457_154969459delinsATG | CA2466849020 | F8 | c.881_883delinsCAT (p.Thr294=) c.*757_*759delinsCAT (n.*757_*759delinsCAT) c.776_778delinsCAT (p.Thr259=) | |
X | g.154969462_154969463del | CA2466849021 | F8 | c.881_882del (p.Thr294IlefsTer?) c.*757_*758del (n.*757_*758del) c.776_777del (p.Thr259IlefsTer?) | dbSNP |
X | g.154969459G>A | CA255077 | F8 | c.881C>T (p.Thr294Ile) c.*757C>T (n.*757C>T) c.776C>T (p.Thr259Ile) | ClinVar dbSNP |
X | g.154969459G>C | CA414918087 | F8 | c.881C>G (p.Thr294Arg) c.*757C>G (n.*757C>G) c.776C>G (p.Thr259Arg) | ClinVar |
X | g.154969459G= | CA2466849022 | F8 | c.881C= (p.Thr294=) c.*757C= (n.*757C=) c.776C= (p.Thr259=) | |
X | g.154969459G>T | CA414918084 | F8 | c.881C>A (p.Thr294Lys) c.*757C>A (n.*757C>A) c.776C>A (p.Thr259Lys) | |
X | g.154969460T>A | CA414918090 | F8 | c.880A>T (p.Thr294Ser) c.*756A>T (n.*756A>T) c.775A>T (p.Thr259Ser) | COSMIC COSMIC |
X | g.154969460T>C | CA414918091 | F8 | c.880A>G (p.Thr294Ala) c.*756A>G (n.*756A>G) c.775A>G (p.Thr259Ala) | |
X | g.154969460T>G | CA414918093 | F8 | c.880A>C (p.Thr294Pro) c.*756A>C (n.*756A>C) c.775A>C (p.Thr259Pro) | |
X | g.154969461G>A | CA10568529 | F8 | c.879C>T (p.His293=) c.*755C>T (n.*755C>T) c.774C>T (p.His258=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154969461G>C | CA414918095 | F8 | c.879C>G (p.His293Gln) c.*755C>G (n.*755C>G) c.774C>G (p.His258Gln) | |
X | g.154969461G= | CA2466849023 | F8 | c.879C= (p.His293=) c.*755C= (n.*755C=) c.774C= (p.His258=) | |
X | g.154969461G>T | CA414918096 | F8 | c.879C>A (p.His293Gln) c.*755C>A (n.*755C>A) c.774C>A (p.His258Gln) | |
X | g.154969462T>A | CA414918098 | F8 | c.878A>T (p.His293Leu) c.*754A>T (n.*754A>T) c.773A>T (p.His258Leu) | |
X | g.154969462T>C | CA414918100 | F8 | c.878A>G (p.His293Arg) c.*754A>G (n.*754A>G) c.773A>G (p.His258Arg) | dbSNP |
X | g.154969462T>G | CA414918102 | F8 | c.878A>C (p.His293Pro) c.*754A>C (n.*754A>C) c.773A>C (p.His258Pro) | gnomAD v4 |
X | g.154969462T= | CA2466849024 | F8 | c.878A= (p.His293=) c.*754A= (n.*754A=) c.773A= (p.His258=) | |
X | g.154969463G>A | CA414918105 | F8 | c.877C>T (p.His293Tyr) c.*753C>T (n.*753C>T) c.772C>T (p.His258Tyr) | |
X | g.154969463G>C | CA414918107 | F8 | c.877C>G (p.His293Asp) c.*753C>G (n.*753C>G) c.772C>G (p.His258Asp) | ClinVar dbSNP |
X | g.154969463G= | CA2466849025 | F8 | c.877C= (p.His293=) c.*753C= (n.*753C=) c.772C= (p.His258=) | |
X | g.154969463G>T | CA414918108 | F8 | c.877C>A (p.His293Asn) c.*753C>A (n.*753C>A) c.772C>A (p.His258Asn) | |
X | g.154969464A>C | CA519367503 | F8 | c.876T>G (p.Gly292=) c.*752T>G (n.*752T>G) c.771T>G (p.Gly257=) | |
X | g.154969464A>G | CA519367504 | F8 | c.876T>C (p.Gly292=) c.*752T>C (n.*752T>C) c.771T>C (p.Gly257=) | |
X | g.154969464A>T | CA519367505 | F8 | c.876T>A (p.Gly292=) c.*752T>A (n.*752T>A) c.771T>A (p.Gly257=) | |
X | g.154969465C>A | CA414918110 | F8 | c.875G>T (p.Gly292Val) c.*751G>T (n.*751G>T) c.770G>T (p.Gly257Val) | |
X | g.154969465C= | CA2466849026 | F8 | c.875G= (p.Gly292=) c.*751G= (n.*751G=) c.770G= (p.Gly257=) | |
X | g.154969465C>G | CA414918114 | F8 | c.875G>C (p.Gly292Ala) c.*751G>C (n.*751G>C) c.770G>C (p.Gly257Ala) | |
X | g.154969465C>T | CA414918112 | F8 | c.875G>A (p.Gly292Asp) c.*751G>A (n.*751G>A) c.770G>A (p.Gly257Asp) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154969466C>A | CA414918116 | F8 | c.874G>T (p.Gly292Cys) c.*750G>T (n.*750G>T) c.769G>T (p.Gly257Cys) | |
X | g.154969466C>G | CA414918120 | F8 | c.874G>C (p.Gly292Arg) c.*750G>C (n.*750G>C) c.769G>C (p.Gly257Arg) | |
X | g.154969466C>T | CA414918121 | F8 | c.874G>A (p.Gly292Ser) c.*750G>A (n.*750G>A) c.769G>A (p.Gly257Ser) | |
X | g.154969467T>A | CA414918122 | F8 | c.873A>T (p.Glu291Asp) c.*749A>T (n.*749A>T) c.768A>T (p.Glu256Asp) | |
X | g.154969467T>C | CA519367512 | F8 | c.873A>G (p.Glu291=) c.*749A>G (n.*749A>G) c.768A>G (p.Glu256=) | |
X | g.154969467T>G | CA414918124 | F8 | c.873A>C (p.Glu291Asp) c.*749A>C (n.*749A>C) c.768A>C (p.Glu256Asp) | |
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 |