Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154896129_154896138del | CA2695237822 | F8 | c.6370_6379del (p.Tyr2124MetfsTer16) c.6265_6274del (p.Tyr2089MetfsTer16) | |
X | g.154896137C>A | CA414899679 | F8 | c.6369G>T (p.Met2123Ile) c.6264G>T (p.Met2088Ile) | |
X | g.154896137C= | CA2466826015 | F8 | c.6369G= (p.Met2123=) c.6264G= (p.Met2088=) | |
X | g.154896137C>G | CA414899676 | F8 | c.6369G>C (p.Met2123Ile) c.6264G>C (p.Met2088Ile) | |
X | g.154896137C>T | CA10567865 | F8 | c.6369G>A (p.Met2123Ile) c.6264G>A (p.Met2088Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154896138A= | CA2466826016 | F8 | c.6368T= (p.Met2123=) c.6263T= (p.Met2088=) | |
X | g.154896138A>C | CA414899683 | F8 | c.6368T>G (p.Met2123Arg) c.6263T>G (p.Met2088Arg) | |
X | g.154896138A>G | CA10567866 | F8 | c.6368T>C (p.Met2123Thr) c.6263T>C (p.Met2088Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154896138A>T | CA414899684 | F8 | c.6368T>A (p.Met2123Lys) c.6263T>A (p.Met2088Lys) | |
X | g.154896139T>A | CA414899687 | F8 | c.6367A>T (p.Met2123Leu) c.6262A>T (p.Met2088Leu) | |
X | g.154896139T>C | CA414899689 | F8 | c.6367A>G (p.Met2123Val) c.6262A>G (p.Met2088Val) | gnomAD v4 |
X | g.154896139T>G | CA414899692 | F8 | c.6367A>C (p.Met2123Leu) c.6262A>C (p.Met2088Leu) | |
X | g.154896140G>A | CA519352626 | F8 | c.6366C>T (p.Ile2122=) c.6261C>T (p.Ile2087=) | |
X | g.154896140G>C | CA414899701 | F8 | c.6366C>G (p.Ile2122Met) c.6261C>G (p.Ile2087Met) | |
X | g.154896140G>T | CA519352629 | F8 | c.6366C>A (p.Ile2122=) c.6261C>A (p.Ile2087=) | |
X | g.154896141A>C | CA414899702 | F8 | c.6365T>G (p.Ile2122Ser) c.6260T>G (p.Ile2087Ser) | |
X | g.154896141A>G | CA414899703 | F8 | c.6365T>C (p.Ile2122Thr) c.6260T>C (p.Ile2087Thr) | |
X | g.154896141A>T | CA414899704 | F8 | c.6365T>A (p.Ile2122Asn) c.6260T>A (p.Ile2087Asn) | |
X | g.154896142T>A | CA414899707 | F8 | c.6364A>T (p.Ile2122Phe) c.6259A>T (p.Ile2087Phe) | |
X | g.154896142T>C | CA414899708 | F8 | c.6364A>G (p.Ile2122Val) c.6259A>G (p.Ile2087Val) | |
X | g.154896142T>G | CA414899711 | F8 | c.6364A>C (p.Ile2122Leu) c.6259A>C (p.Ile2087Leu) | |
X | g.154896143G>A | CA519352641 | F8 | c.6363C>T (p.Ile2121=) c.6258C>T (p.Ile2086=) | |
X | g.154896143G>C | CA414899715 | F8 | c.6363C>G (p.Ile2121Met) c.6258C>G (p.Ile2086Met) | |
X | g.154896143G>T | CA519352644 | F8 | c.6363C>A (p.Ile2121=) c.6258C>A (p.Ile2086=) | |
X | g.154896144A= | CA2466826018 | F8 | c.6362T= (p.Ile2121=) c.6257T= (p.Ile2086=) | |
X | g.154896144A>C | CA414899720 | F8 | c.6362T>G (p.Ile2121Ser) c.6257T>G (p.Ile2086Ser) | |
X | g.154896144A>G | CA414899721 | F8 | c.6362T>C (p.Ile2121Thr) c.6257T>C (p.Ile2086Thr) | dbSNP gnomAD v4 |
X | g.154896144A>T | CA414899722 | F8 | c.6362T>A (p.Ile2121Asn) c.6257T>A (p.Ile2086Asn) | ClinVar |
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) |