Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154896144_154896149delinsATAAAC | CA2466826017 | F8 | c.6357_6362delinsGTTTAT (p.Gln2119=) c.6252_6257delinsGTTTAT (p.Gln2084=) | |
X | g.154896145T>A | CA414899725 | F8 | c.6361A>T (p.Ile2121Phe) c.6256A>T (p.Ile2086Phe) | |
X | g.154896145T>C | CA414899729 | F8 | c.6361A>G (p.Ile2121Val) c.6256A>G (p.Ile2086Val) | |
X | g.154896145T>G | CA414899733 | F8 | c.6361A>C (p.Ile2121Leu) c.6256A>C (p.Ile2086Leu) | |
X | g.154896146_154896150del | CA873337992 | F8 | c.6357_6361del (p.Gln2119HisfsTer5) c.6252_6256del (p.Gln2084HisfsTer5) | dbSNP |
X | g.154896146A= | CA2466826019 | F8 | c.6360T= (p.Phe2120=) c.6255T= (p.Phe2085=) | |
X | g.154896146A>C | CA255202 | F8 | c.6360T>G (p.Phe2120Leu) c.6255T>G (p.Phe2085Leu) | ClinVar dbSNP |
X | g.154896146A>G | CA519352656 | F8 | c.6360T>C (p.Phe2120=) c.6255T>C (p.Phe2085=) | |
X | g.154896146A>T | CA414899736 | F8 | c.6360T>A (p.Phe2120Leu) c.6255T>A (p.Phe2085Leu) | |
X | g.154896147A>C | CA414899743 | F8 | c.6359T>G (p.Phe2120Cys) c.6254T>G (p.Phe2085Cys) | |
X | g.154896147A>G | CA414899745 | F8 | c.6359T>C (p.Phe2120Ser) c.6254T>C (p.Phe2085Ser) | |
X | g.154896147A>T | CA414899746 | F8 | c.6359T>A (p.Phe2120Tyr) c.6254T>A (p.Phe2085Tyr) | |
X | g.154896148A>C | CA414899759 | F8 | c.6358T>G (p.Phe2120Val) c.6253T>G (p.Phe2085Val) | |
X | g.154896148A>G | CA414899758 | F8 | c.6358T>C (p.Phe2120Leu) c.6253T>C (p.Phe2085Leu) | COSMIC COSMIC |
X | g.154896148A>T | CA414899752 | F8 | c.6358T>A (p.Phe2120Ile) c.6253T>A (p.Phe2085Ile) | |
X | g.154896149C>A | CA414899762 | F8 | c.6357G>T (p.Gln2119His) c.6252G>T (p.Gln2084His) | |
X | g.154896149C= | CA2466826020 | F8 | c.6357G= (p.Gln2119=) c.6252G= (p.Gln2084=) | |
X | g.154896149C>G | CA414899763 | F8 | c.6357G>C (p.Gln2119His) c.6252G>C (p.Gln2084His) | |
X | g.154896149C>T | CA519352672 | F8 | c.6357G>A (p.Gln2119=) c.6252G>A (p.Gln2084=) | dbSNP gnomAD v3 gnomAD v4 |
X | g.154896150T>A | CA414899764 | F8 | c.6356A>T (p.Gln2119Leu) c.6251A>T (p.Gln2084Leu) | |
X | g.154896150T>C | CA414899765 | F8 | c.6356A>G (p.Gln2119Arg) c.6251A>G (p.Gln2084Arg) | |
X | g.154896150T>G | CA414899766 | F8 | c.6356A>C (p.Gln2119Pro) c.6251A>C (p.Gln2084Pro) | |
X | g.154896150_154896151del | CA2695237824 | F8 | c.6355_6356del (p.Gln2119ValfsTer6) c.6250_6251del (p.Gln2084ValfsTer6) | |
X | g.154896151del | CA2695237825 | F8 | c.6355del (p.Gln2119SerfsTer24) c.6250del (p.Gln2084SerfsTer24) | |
X | g.154896151G>A | CA414899773 | F8 | c.6355C>T (p.Gln2119Ter) c.6250C>T (p.Gln2084Ter) | ClinVar dbSNP |
X | g.154896151G>C | CA414899775 | F8 | c.6355C>G (p.Gln2119Glu) c.6250C>G (p.Gln2084Glu) | dbSNP |
X | g.154896151G= | CA2466826021 | F8 | c.6355C= (p.Gln2119=) c.6250C= (p.Gln2084=) | |
X | g.154896151G>T | CA414899776 | F8 | c.6355C>A (p.Gln2119Lys) c.6250C>A (p.Gln2084Lys) | |
X | g.154896152A>C | CA519352684 | F8 | c.6354T>G (p.Ser2118=) c.6249T>G (p.Ser2083=) | |
X | g.154896152A>G | CA519352686 | F8 | c.6354T>C (p.Ser2118=) c.6249T>C (p.Ser2083=) | |
X | g.154896152A>T | CA519352688 | F8 | c.6354T>A (p.Ser2118=) c.6249T>A (p.Ser2083=) | |
X | g.154896153G>A | CA414899781 | F8 | c.6353C>T (p.Ser2118Phe) c.6248C>T (p.Ser2083Phe) | |
X | g.154896153G>C | CA414899785 | F8 | c.6353C>G (p.Ser2118Cys) c.6248C>G (p.Ser2083Cys) | |
X | g.154896153G>T | CA414899789 | F8 | c.6353C>A (p.Ser2118Tyr) c.6248C>A (p.Ser2083Tyr) | |
X | g.154896154A>C | CA414899799 | F8 | c.6352T>G (p.Ser2118Ala) c.6247T>G (p.Ser2083Ala) | |
X | g.154896154A>G | CA414899798 | F8 | c.6352T>C (p.Ser2118Pro) c.6247T>C (p.Ser2083Pro) | |
X | g.154896154A>T | CA414899797 | F8 | c.6352T>A (p.Ser2118Thr) c.6247T>A (p.Ser2083Thr) | |
X | g.154896155G>A | CA519352699 | F8 | c.6351C>T (p.Ile2117=) c.6246C>T (p.Ile2082=) | |
X | g.154896155G>C | CA414899801 | F8 | c.6351C>G (p.Ile2117Met) c.6246C>G (p.Ile2082Met) | |
X | g.154896155G>T | CA519352702 | F8 | c.6351C>A (p.Ile2117=) c.6246C>A (p.Ile2082=) | gnomAD v4 |
X | g.154896156A>C | CA414899803 | F8 | c.6350T>G (p.Ile2117Ser) c.6245T>G (p.Ile2082Ser) | |
X | g.154896156A>G | CA414899805 | F8 | c.6350T>C (p.Ile2117Thr) c.6245T>C (p.Ile2082Thr) | |
X | g.154896156A>T | CA414899808 | F8 | c.6350T>A (p.Ile2117Asn) c.6245T>A (p.Ile2082Asn) | |
X | g.154896157T>A | CA414899811 | F8 | c.6349A>T (p.Ile2117Phe) c.6244A>T (p.Ile2082Phe) | dbSNP |
X | g.154896157T>C | CA414899813 | F8 | c.6349A>G (p.Ile2117Val) c.6244A>G (p.Ile2082Val) | gnomAD v4 |
X | g.154896157T>G | CA414899822 | F8 | c.6349A>C (p.Ile2117Leu) c.6244A>C (p.Ile2082Leu) | |
X | g.154896157T= | CA2466826022 | F8 | c.6349A= (p.Ile2117=) c.6244A= (p.Ile2082=) | |
X | g.154896158G>A | CA519352714 | F8 | c.6348C>T (p.Tyr2116=) c.6243C>T (p.Tyr2081=) | gnomAD v4 |
X | g.154896158G>C | CA414899824 | F8 | c.6348C>G (p.Tyr2116Ter) c.6243C>G (p.Tyr2081Ter) | |
X | g.154896158G>T | CA414899825 | F8 | c.6348C>A (p.Tyr2116Ter) c.6243C>A (p.Tyr2081Ter) |