11 | g.22625314T>A | CA380058921 | FANCF | c.497A>T (p.Gln166Leu)
| |
11 | g.22625314T>C | CA380058922 | FANCF | c.497A>G (p.Gln166Arg)
| |
11 | g.22625314T>G | CA380058923 | FANCF | c.497A>C (p.Gln166Pro)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625314T= | CA1957607138 | FANCF | c.497A= (p.Gln166=)
| |
11 | g.22625315G>A | CA380058924 | FANCF | c.496C>T (p.Gln166Ter)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625315G>C | CA380058925 | FANCF | c.496C>G (p.Gln166Glu)
| |
11 | g.22625315G= | CA1957607139 | FANCF | c.496C= (p.Gln166=)
| |
11 | g.22625315G>T | CA5924320 | FANCF | c.496C>A (p.Gln166Lys)
| dbSNP ExAC |
11 | g.22625316G>A | CA473533525 | FANCF | c.495C>T (p.Thr165=)
| |
11 | g.22625316G>C | CA473533523 | FANCF | c.495C>G (p.Thr165=)
| dbSNP |
11 | g.22625316G>T | CA473533524 | FANCF | c.495C>A (p.Thr165=)
| |
11 | g.22625317G>A | CA380058926 | FANCF | c.494C>T (p.Thr165Ile)
| ClinVar gnomAD v4 |
11 | g.22625317G>C | CA380058927 | FANCF | c.494C>G (p.Thr165Ser)
| dbSNP |
11 | g.22625317G>T | CA380058928 | FANCF | c.494C>A (p.Thr165Asn)
| |
11 | g.22625318T>A | CA380058929 | FANCF | c.493A>T (p.Thr165Ser)
| |
11 | g.22625318T>C | CA380058930 | FANCF | c.493A>G (p.Thr165Ala)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625318T>G | CA380058931 | FANCF | c.493A>C (p.Thr165Pro)
| dbSNP |
11 | g.22625318T= | CA1957607140 | FANCF | c.493A= (p.Thr165=)
| |
11 | g.22625319C>A | CA380058933 | FANCF | c.492G>T (p.Lys164Asn)
| |
11 | g.22625319C>G | CA380058932 | FANCF | c.492G>C (p.Lys164Asn)
| |
11 | g.22625319C>T | CA473533526 | FANCF | c.492G>A (p.Lys164=)
| gnomAD v4 |
11 | g.22625320T>A | CA380058934 | FANCF | c.491A>T (p.Lys164Met)
| |
11 | g.22625320T>C | CA380058936 | FANCF | c.491A>G (p.Lys164Arg)
| |
11 | g.22625320T>G | CA380058935 | FANCF | c.491A>C (p.Lys164Thr)
| |
11 | g.22625321T>A | CA380058937 | FANCF | c.490A>T (p.Lys164Ter)
| |
11 | g.22625321T>C | CA380058938 | FANCF | c.490A>G (p.Lys164Glu)
| |
11 | g.22625321T>G | CA380058939 | FANCF | c.490A>C (p.Lys164Gln)
| |
11 | g.22625322C>A | CA380058940 | FANCF | c.489G>T (p.Met163Ile)
| |
11 | g.22625322C= | CA1957607141 | FANCF | c.489G= (p.Met163=)
| |
11 | g.22625322C>G | CA380058941 | FANCF | c.489G>C (p.Met163Ile)
| ClinVar dbSNP |
11 | g.22625322C>T | CA380058942 | FANCF | c.489G>A (p.Met163Ile)
| gnomAD v4 |
11 | g.22625323A>C | CA380058945 | FANCF | c.488T>G (p.Met163Arg)
| |
11 | g.22625323A>G | CA380058943 | FANCF | c.488T>C (p.Met163Thr)
| |
11 | g.22625323A>T | CA380058944 | FANCF | c.488T>A (p.Met163Lys)
| |
11 | g.22625324T>A | CA380058946 | FANCF | c.487A>T (p.Met163Leu)
| |
11 | g.22625324T>C | CA380058947 | FANCF | c.487A>G (p.Met163Val)
| |
11 | g.22625324T>G | CA380058948 | FANCF | c.487A>C (p.Met163Leu)
| |
11 | g.22625325C>A | CA5924321 | FANCF | c.486G>T (p.Leu162=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625325C= | CA1957607143 | FANCF | c.486G= (p.Leu162=)
| |
11 | g.22625325C>G | CA473533527 | FANCF | c.486G>C (p.Leu162=)
| |
11 | g.22625325C>T | CA473533528 | FANCF | c.486G>A (p.Leu162=)
| |
11 | g.22625325_22625327delinsCAG | CA1957607142 | FANCF | c.484_486delinsCTG (p.Leu162=)
| |
11 | g.22625326A>C | CA380058949 | FANCF | c.485T>G (p.Leu162Arg)
| |
11 | g.22625326A>G | CA380058951 | FANCF | c.485T>C (p.Leu162Pro)
| gnomAD v4 |
11 | g.22625326A>T | CA380058950 | FANCF | c.485T>A (p.Leu162Gln)
| |
11 | g.22625330_22625331del | CA213089 | FANCF | c.484_485del (p.Leu162AspfsTer?)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625327G>A | CA473533529 | FANCF | c.484C>T (p.Leu162=)
| |
11 | g.22625327G>C | CA380058952 | FANCF | c.484C>G (p.Leu162Val)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625327G>T | CA380058953 | FANCF | c.484C>A (p.Leu162Met)
| |
11 | g.22625328A>C | CA473533530 | FANCF | c.483T>G (p.Ser161=)
| |
11 | g.22625328A>G | CA473533531 | FANCF | c.483T>C (p.Ser161=)
| |
11 | g.22625328A>T | CA473533532 | FANCF | c.483T>A (p.Ser161=)
| |
11 | g.22625329G>A | CA380058954 | FANCF | c.482C>T (p.Ser161Phe)
| |
11 | g.22625329G>C | CA380058955 | FANCF | c.482C>G (p.Ser161Cys)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625329G= | CA1957607144 | FANCF | c.482C= (p.Ser161=)
| |
11 | g.22625329G>T | CA380058956 | FANCF | c.482C>A (p.Ser161Tyr)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625330A>C | CA380058957 | FANCF | c.481T>G (p.Ser161Ala)
| |
11 | g.22625330A>G | CA380058958 | FANCF | c.481T>C (p.Ser161Pro)
| |
11 | g.22625330A>T | CA380058959 | FANCF | c.481T>A (p.Ser161Thr)
| |
11 | g.22625331G>A | CA473533533 | FANCF | c.480C>T (p.Asp160=)
| COSMIC |
11 | g.22625331G>C | CA380058961 | FANCF | c.480C>G (p.Asp160Glu)
| gnomAD v4 COSMIC |
11 | g.22625331G>T | CA380058960 | FANCF | c.480C>A (p.Asp160Glu)
| |
11 | g.22625332T>A | CA380058962 | FANCF | c.479A>T (p.Asp160Val)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625332T>C | CA380058963 | FANCF | c.479A>G (p.Asp160Gly)
| |
11 | g.22625332T>G | CA380058964 | FANCF | c.479A>C (p.Asp160Ala)
| |
11 | g.22625332T= | CA1957607145 | FANCF | c.479A= (p.Asp160=)
| |
11 | g.22625336_22625338del | CA2612850468 | FANCF | c.477_479del (p.Glu159del)
| gnomAD v4 |
11 | g.22625333C>A | CA380058965 | FANCF | c.478G>T (p.Asp160Tyr)
| dbSNP gnomAD v2 |
11 | g.22625333C= | CA1957607146 | FANCF | c.478G= (p.Asp160=)
| |
11 | g.22625333C>G | CA380058966 | FANCF | c.478G>C (p.Asp160His)
| |
11 | g.22625333C>T | CA380058967 | FANCF | c.478G>A (p.Asp160Asn)
| gnomAD v4 COSMIC |
11 | g.22625334C>A | CA380058968 | FANCF | c.477G>T (p.Glu159Asp)
| |
11 | g.22625334C>G | CA380058969 | FANCF | c.477G>C (p.Glu159Asp)
| |
11 | g.22625334C>T | CA473533534 | FANCF | c.477G>A (p.Glu159=)
| ClinVar dbSNP |
11 | g.22625335T>A | CA380058970 | FANCF | c.476A>T (p.Glu159Val)
| dbSNP |
11 | g.22625335T>C | CA380058971 | FANCF | c.476A>G (p.Glu159Gly)
| |
11 | g.22625335T>G | CA380058972 | FANCF | c.476A>C (p.Glu159Ala)
| |
11 | g.22625336C>A | CA380058973 | FANCF | c.475G>T (p.Glu159Ter)
| |
11 | g.22625336C= | CA1957607147 | FANCF | c.475G= (p.Glu159=)
| |
11 | g.22625336C>G | CA380058974 | FANCF | c.475G>C (p.Glu159Gln)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625336C>T | CA380058975 | FANCF | c.475G>A (p.Glu159Lys)
| dbSNP gnomAD v4 |
11 | g.22625337C>A | CA380058977 | FANCF | c.474G>T (p.Gln158His)
| |
11 | g.22625337C= | CA1957607148 | FANCF | c.474G= (p.Gln158=)
| |
11 | g.22625337C>G | CA380058976 | FANCF | c.474G>C (p.Gln158His)
| dbSNP |
11 | g.22625337C>T | CA473533536 | FANCF | c.474G>A (p.Gln158=)
| ClinVar dbSNP |
11 | g.22625338T>A | CA380058978 | FANCF | c.473A>T (p.Gln158Leu)
| |
11 | g.22625338T>C | CA380058979 | FANCF | c.473A>G (p.Gln158Arg)
| ClinVar COSMIC |
11 | g.22625338T>G | CA380058980 | FANCF | c.473A>C (p.Gln158Pro)
| |
11 | g.22625339G>A | CA380058981 | FANCF | c.472C>T (p.Gln158Ter)
| |
11 | g.22625339G>C | CA380058982 | FANCF | c.472C>G (p.Gln158Glu)
| |
11 | g.22625339G>T | CA380058983 | FANCF | c.472C>A (p.Gln158Lys)
| |
11 | g.22625340G>A | CA5924323 | FANCF | c.471C>T (p.Leu157=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625340G>C | CA473533539 | FANCF | c.471C>G (p.Leu157=)
| |
11 | g.22625340G= | CA1957607149 | FANCF | c.471C= (p.Leu157=)
| |
11 | g.22625340G>T | CA5924322 | FANCF | c.471C>A (p.Leu157=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625341A>C | CA380058984 | FANCF | c.470T>G (p.Leu157Arg)
| |
11 | g.22625341A>G | CA380058985 | FANCF | c.470T>C (p.Leu157Pro)
| gnomAD v4 |
11 | g.22625341A>T | CA380058986 | FANCF | c.470T>A (p.Leu157His)
| |
11 | g.22625342G>A | CA16613287 | FANCF | c.469C>T (p.Leu157Phe)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625342G>C | CA380058987 | FANCF | c.469C>G (p.Leu157Val)
| |
11 | g.22625342G= | CA1957607150 | FANCF | c.469C= (p.Leu157=)
| |
11 | g.22625342G>T | CA380058988 | FANCF | c.469C>A (p.Leu157Ile)
| gnomAD v4 COSMIC |
11 | g.22625343A>C | CA380058989 | FANCF | c.468T>G (p.Asn156Lys)
| |
11 | g.22625343A>G | CA473533541 | FANCF | c.468T>C (p.Asn156=)
| |
11 | g.22625343A>T | CA380058990 | FANCF | c.468T>A (p.Asn156Lys)
| |
11 | g.22625344T>A | CA380058991 | FANCF | c.467A>T (p.Asn156Ile)
| |
11 | g.22625344T>C | CA380058993 | FANCF | c.467A>G (p.Asn156Ser)
| gnomAD v4 |
11 | g.22625344T>G | CA380058992 | FANCF | c.467A>C (p.Asn156Thr)
| |
11 | g.22625345T>A | CA380058994 | FANCF | c.466A>T (p.Asn156Tyr)
| |
11 | g.22625345T>C | CA5924324 | FANCF | c.466A>G (p.Asn156Asp)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625345T>G | CA5924325 | FANCF | c.466A>C (p.Asn156His)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625345T= | CA1957607151 | FANCF | c.466A= (p.Asn156=)
| |
11 | g.22625346T>A | CA5924326 | FANCF | c.465A>T (p.Pro155=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625346T>C | CA473533544 | FANCF | c.465A>G (p.Pro155=)
| gnomAD v4 |
11 | g.22625346T>G | CA473533545 | FANCF | c.465A>C (p.Pro155=)
| gnomAD v4 |
11 | g.22625346T= | CA1957607152 | FANCF | c.465A= (p.Pro155=)
| |
11 | g.22625347G>A | CA380058995 | FANCF | c.464C>T (p.Pro155Leu)
| dbSNP |
11 | g.22625347G>C | CA380058996 | FANCF | c.464C>G (p.Pro155Arg)
| |
11 | g.22625347G>T | CA380058997 | FANCF | c.464C>A (p.Pro155Gln)
| |
11 | g.22625348G>A | CA380058998 | FANCF | c.463C>T (p.Pro155Ser)
| |
11 | g.22625348G>C | CA380058999 | FANCF | c.463C>G (p.Pro155Ala)
| dbSNP |
11 | g.22625348G>T | CA380059000 | FANCF | c.463C>A (p.Pro155Thr)
| dbSNP |
11 | g.22625349G>A | CA473533547 | FANCF | c.462C>T (p.Asn154=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625349G>C | CA380059001 | FANCF | c.462C>G (p.Asn154Lys)
| |
11 | g.22625349G>T | CA380059002 | FANCF | c.462C>A (p.Asn154Lys)
| ClinVar gnomAD v4 |
11 | g.22625350T>A | CA380059003 | FANCF | c.461A>T (p.Asn154Ile)
| |
11 | g.22625350T>C | CA380059004 | FANCF | c.461A>G (p.Asn154Ser)
| |
11 | g.22625350T>G | CA380059005 | FANCF | c.461A>C (p.Asn154Thr)
| |
11 | g.22625351T>A | CA380059008 | FANCF | c.460A>T (p.Asn154Tyr)
| |
11 | g.22625351T>C | CA380059006 | FANCF | c.460A>G (p.Asn154Asp)
| |
11 | g.22625351T>G | CA380059007 | FANCF | c.460A>C (p.Asn154His)
| |
11 | g.22625356_22625357del | CA2612850469 | FANCF | c.459_460del (p.Asn154ProfsTer?)
| gnomAD v4 |
11 | g.22625352C>A | CA380059009 | FANCF | c.459G>T (p.Glu153Asp)
| |
11 | g.22625352C>G | CA380059010 | FANCF | c.459G>C (p.Glu153Asp)
| |
11 | g.22625352C>T | CA473533551 | FANCF | c.459G>A (p.Glu153=)
| gnomAD v4 |
11 | g.22625353T>A | CA380059011 | FANCF | c.458A>T (p.Glu153Val)
| |
11 | g.22625353T>C | CA380059012 | FANCF | c.458A>G (p.Glu153Gly)
| |
11 | g.22625353T>G | CA380059013 | FANCF | c.458A>C (p.Glu153Ala)
| |
11 | g.22625354C>A | CA380059014 | FANCF | c.457G>T (p.Glu153Ter)
| |
11 | g.22625354C= | CA1957607153 | FANCF | c.457G= (p.Glu153=)
| |
11 | g.22625354C>G | CA5924327 | FANCF | c.457G>C (p.Glu153Gln)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625354C>T | CA380059015 | FANCF | c.457G>A (p.Glu153Lys)
| ClinVar dbSNP |
11 | g.22625355T>A | CA380059016 | FANCF | c.456A>T (p.Arg152Ser)
| |
11 | g.22625355T>C | CA473533552 | FANCF | c.456A>G (p.Arg152=)
| gnomAD v4 |
11 | g.22625355T>G | CA380059017 | FANCF | c.456A>C (p.Arg152Ser)
| |
11 | g.22625356del | CA2790714009 | FANCF | c.455del (p.Arg152LysfsTer11)
| |
11 | g.22625356C>A | CA380059019 | FANCF | c.455G>T (p.Arg152Ile)
| |
11 | g.22625356C= | CA1957607154 | FANCF | c.455G= (p.Arg152=)
| |
11 | g.22625356C>G | CA380059018 | FANCF | c.455G>C (p.Arg152Thr)
| |
11 | g.22625356C>T | CA219086641 | FANCF | c.455G>A (p.Arg152Lys)
| dbSNP gnomAD v4 COSMIC |
11 | g.22625357T>A | CA380059020 | FANCF | c.454A>T (p.Arg152Ter)
| |
11 | g.22625357T>C | CA380059021 | FANCF | c.454A>G (p.Arg152Gly)
| gnomAD v4 |
11 | g.22625357T>G | CA473533554 | FANCF | c.454A>C (p.Arg152=)
| |
11 | g.22625359_22625360del | CA2612850470 | FANCF | c.453_454del (p.Tyr151Ter)
| gnomAD v4 |
11 | g.22625358A>C | CA380059022 | FANCF | c.453T>G (p.Tyr151Ter)
| |
11 | g.22625358A>G | CA473533555 | FANCF | c.453T>C (p.Tyr151=)
| gnomAD v4 |
11 | g.22625358A>T | CA380059023 | FANCF | c.453T>A (p.Tyr151Ter)
| gnomAD v4 |
11 | g.22625359T>A | CA5924328 | FANCF | c.452A>T (p.Tyr151Phe)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625359T>C | CA380059024 | FANCF | c.452A>G (p.Tyr151Cys)
| gnomAD v4 |
11 | g.22625359T>G | CA380059025 | FANCF | c.452A>C (p.Tyr151Ser)
| |
11 | g.22625359T= | CA1957607156 | FANCF | c.452A= (p.Tyr151=)
| |
11 | g.22625359_22625373delinsTAGCCATTGAAGCGC | CA1957607155 | FANCF | c.438_452delinsGCGCTTCAATGGCTA (p.Leu146=)
| |
11 | g.22625360A= | CA1957607157 | FANCF | c.451T= (p.Tyr151=)
| |
11 | g.22625360A>C | CA380059026 | FANCF | c.451T>G (p.Tyr151Asp)
| gnomAD v4 |
11 | g.22625360A>G | CA380059027 | FANCF | c.451T>C (p.Tyr151His)
| gnomAD v4 |
11 | g.22625360A>T | CA219086642 | FANCF | c.451T>A (p.Tyr151Asn)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625363_22625376del | CA5924329 | FANCF | c.438_451del (p.Arg147Ter)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625361G>A | CA473533559 | FANCF | c.450C>T (p.Gly150=)
| |
11 | g.22625361G>C | CA473533560 | FANCF | c.450C>G (p.Gly150=)
| |
11 | g.22625361G>T | CA473533561 | FANCF | c.450C>A (p.Gly150=)
| |
11 | g.22625362C>A | CA380059028 | FANCF | c.449G>T (p.Gly150Val)
| dbSNP |
11 | g.22625362C= | CA1957607158 | FANCF | c.449G= (p.Gly150=)
| |
11 | g.22625362C>G | CA380059029 | FANCF | c.449G>C (p.Gly150Ala)
| dbSNP gnomAD v4 |
11 | g.22625362C>T | CA380059030 | FANCF | c.449G>A (p.Gly150Asp)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625363C>A | CA380059031 | FANCF | c.448G>T (p.Gly150Cys)
| |
11 | g.22625363C= | CA1957607159 | FANCF | c.448G= (p.Gly150=)
| |
11 | g.22625363C>G | CA380059032 | FANCF | c.448G>C (p.Gly150Arg)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625363C>T | CA219086643 | FANCF | c.448G>A (p.Gly150Ser)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625364A>C | CA380059033 | FANCF | c.447T>G (p.Asn149Lys)
| |
11 | g.22625364A>G | CA473533565 | FANCF | c.447T>C (p.Asn149=)
| ClinVar |
11 | g.22625364A>T | CA380059034 | FANCF | c.447T>A (p.Asn149Lys)
| |
11 | g.22625365T>A | CA380059035 | FANCF | c.446A>T (p.Asn149Ile)
| |
11 | g.22625365T>C | CA5924330 | FANCF | c.446A>G (p.Asn149Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625365T>G | CA380059036 | FANCF | c.446A>C (p.Asn149Thr)
| |
11 | g.22625365T= | CA1957607160 | FANCF | c.446A= (p.Asn149=)
| |
11 | g.22625366T>A | CA380059037 | FANCF | c.445A>T (p.Asn149Tyr)
| |
11 | g.22625366T>C | CA380059038 | FANCF | c.445A>G (p.Asn149Asp)
| ClinVar |
11 | g.22625366T>G | CA380059039 | FANCF | c.445A>C (p.Asn149His)
| |
11 | g.22625367G>A | CA473533566 | FANCF | c.444C>T (p.Phe148=)
| |
11 | g.22625367G>C | CA380059040 | FANCF | c.444C>G (p.Phe148Leu)
| |
11 | g.22625367G>T | CA380059041 | FANCF | c.444C>A (p.Phe148Leu)
| dbSNP |
11 | g.22625368A>C | CA380059044 | FANCF | c.443T>G (p.Phe148Cys)
| |
11 | g.22625368A>G | CA380059043 | FANCF | c.443T>C (p.Phe148Ser)
| |
11 | g.22625368A>T | CA380059042 | FANCF | c.443T>A (p.Phe148Tyr)
| dbSNP |
11 | g.22625369A>C | CA380059045 | FANCF | c.442T>G (p.Phe148Val)
| gnomAD v4 |
11 | g.22625369A>G | CA380059047 | FANCF | c.442T>C (p.Phe148Leu)
| gnomAD v4 |
11 | g.22625369A>T | CA380059046 | FANCF | c.442T>A (p.Phe148Ile)
| |
11 | g.22625370G>A | CA473533567 | FANCF | c.441C>T (p.Arg147=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625370G>C | CA473533570 | FANCF | c.441C>G (p.Arg147=)
| |
11 | g.22625370G= | CA1957607161 | FANCF | c.441C= (p.Arg147=)
| |
11 | g.22625370G>T | CA473533568 | FANCF | c.441C>A (p.Arg147=)
| |
11 | g.22625371C>A | CA380059048 | FANCF | c.440G>T (p.Arg147Leu)
| |
11 | g.22625371C>G | CA380059049 | FANCF | c.440G>C (p.Arg147Pro)
| |
11 | g.22625371C>T | CA380059050 | FANCF | c.440G>A (p.Arg147His)
| |
11 | g.22625372G>A | CA380059051 | FANCF | c.439C>T (p.Arg147Cys)
| dbSNP |
11 | g.22625372G>C | CA380059052 | FANCF | c.439C>G (p.Arg147Gly)
| |
11 | g.22625372G>T | CA380059053 | FANCF | c.439C>A (p.Arg147Ser)
| |
11 | g.22625373C>A | CA473533574 | FANCF | c.438G>T (p.Leu146=)
| |
11 | g.22625373C= | CA1957607162 | FANCF | c.438G= (p.Leu146=)
| |
11 | g.22625373C>G | CA473533575 | FANCF | c.438G>C (p.Leu146=)
| |
11 | g.22625373C>T | CA473533576 | FANCF | c.438G>A (p.Leu146=)
| dbSNP gnomAD v4 |
11 | g.22625374A>C | CA380059054 | FANCF | c.437T>G (p.Leu146Arg)
| |
11 | g.22625374A>G | CA380059055 | FANCF | c.437T>C (p.Leu146Pro)
| |
11 | g.22625374A>T | CA380059056 | FANCF | c.437T>A (p.Leu146Gln)
| |
11 | g.22625375G>A | CA473533577 | FANCF | c.436C>T (p.Leu146=)
| dbSNP |
11 | g.22625375G>C | CA5924331 | FANCF | c.436C>G (p.Leu146Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625375G= | CA1957607163 | FANCF | c.436C= (p.Leu146=)
| |
11 | g.22625375G>T | CA380059057 | FANCF | c.436C>A (p.Leu146Met)
| |
11 | g.22625376C>A | CA380059060 | FANCF | c.435G>T (p.Met145Ile)
| dbSNP |
11 | g.22625376C>G | CA380059058 | FANCF | c.435G>C (p.Met145Ile)
| dbSNP |
11 | g.22625376C>T | CA380059059 | FANCF | c.435G>A (p.Met145Ile)
| |
11 | g.22625376_22625377delinsCA | CA1957607164 | FANCF | c.434_435delinsTG (p.Met145=)
| |
11 | g.22625377del | CA598390431 | FANCF | c.434del (p.Met145SerfsTer18)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625377A= | CA1957607165 | FANCF | c.434T= (p.Met145=)
| |
11 | g.22625377A>C | CA5924332 | FANCF | c.434T>G (p.Met145Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625377A>G | CA380059061 | FANCF | c.434T>C (p.Met145Thr)
| |
11 | g.22625377A>T | CA380059062 | FANCF | c.434T>A (p.Met145Lys)
| |
11 | g.22625378T>A | CA5924333 | FANCF | c.433A>T (p.Met145Leu)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625378T>C | CA219086644 | FANCF | c.433A>G (p.Met145Val)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625378T>G | CA380059063 | FANCF | c.433A>C (p.Met145Leu)
| gnomAD v4 |
11 | g.22625378T= | CA1957607166 | FANCF | c.433A= (p.Met145=)
| |
11 | g.22625379G>A | CA473533583 | FANCF | c.432C>T (p.His144=)
| |
11 | g.22625379G>C | CA380059064 | FANCF | c.432C>G (p.His144Gln)
| |
11 | g.22625379G= | CA1957607167 | FANCF | c.432C= (p.His144=)
| |
11 | g.22625379G>T | CA5924334 | FANCF | c.432C>A (p.His144Gln)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625380T>A | CA380059065 | FANCF | c.431A>T (p.His144Leu)
| dbSNP |
11 | g.22625380T>C | CA380059066 | FANCF | c.431A>G (p.His144Arg)
| gnomAD v4 |
11 | g.22625380T>G | CA380059067 | FANCF | c.431A>C (p.His144Pro)
| |
11 | g.22625381G>A | CA380059069 | FANCF | c.430C>T (p.His144Tyr)
| dbSNP |
11 | g.22625381G>C | CA380059070 | FANCF | c.430C>G (p.His144Asp)
| |
11 | g.22625381G>T | CA380059068 | FANCF | c.430C>A (p.His144Asn)
| |
11 | g.22625382C>A | CA473533584 | FANCF | c.429G>T (p.Val143=)
| |
11 | g.22625382C= | CA1957607168 | FANCF | c.429G= (p.Val143=)
| |
11 | g.22625382C>G | CA473533585 | FANCF | c.429G>C (p.Val143=)
| |
11 | g.22625382C>T | CA473533586 | FANCF | c.429G>A (p.Val143=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625383A= | CA1957607169 | FANCF | c.428T= (p.Val143=)
| |
11 | g.22625383A>C | CA380059071 | FANCF | c.428T>G (p.Val143Gly)
| dbSNP |
11 | g.22625383A>G | CA380059072 | FANCF | c.428T>C (p.Val143Ala)
| |
11 | g.22625383A>T | CA380059073 | FANCF | c.428T>A (p.Val143Glu)
| |
11 | g.22625384C>A | CA380059074 | FANCF | c.427G>T (p.Val143Leu)
| |
11 | g.22625384C= | CA1957607170 | FANCF | c.427G= (p.Val143=)
| |
11 | g.22625384C>G | CA380059075 | FANCF | c.427G>C (p.Val143Leu)
| |
11 | g.22625384C>T | CA380059076 | FANCF | c.427G>A (p.Val143Met)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625385C>A | CA473533592 | FANCF | c.426G>T (p.Ala142=)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625385C= | CA1957607171 | FANCF | c.426G= (p.Ala142=)
| |
11 | g.22625385C>G | CA473533590 | FANCF | c.426G>C (p.Ala142=)
| |
11 | g.22625385C>T | CA473533591 | FANCF | c.426G>A (p.Ala142=)
| dbSNP gnomAD v4 |
11 | g.22625386G>A | CA380059077 | FANCF | c.425C>T (p.Ala142Val)
| dbSNP |
11 | g.22625386G>C | CA380059078 | FANCF | c.425C>G (p.Ala142Gly)
| |
11 | g.22625386G= | CA1957607172 | FANCF | c.425C= (p.Ala142=)
| |
11 | g.22625386G>T | CA5924335 | FANCF | c.425C>A (p.Ala142Glu)
| dbSNP ExAC gnomAD v4 COSMIC |
11 | g.22625387C>A | CA380059079 | FANCF | c.424G>T (p.Ala142Ser)
| dbSNP |
11 | g.22625387C>G | CA380059080 | FANCF | c.424G>C (p.Ala142Pro)
| |
11 | g.22625387C>T | CA380059081 | FANCF | c.424G>A (p.Ala142Thr)
| |
11 | g.22625388A>C | CA473533595 | FANCF | c.423T>G (p.Ser141=)
| |
11 | g.22625388A>G | CA473533596 | FANCF | c.423T>C (p.Ser141=)
| dbSNP |
11 | g.22625388A>T | CA473533597 | FANCF | c.423T>A (p.Ser141=)
| |
11 | g.22625389G>A | CA380059083 | FANCF | c.422C>T (p.Ser141Phe)
| dbSNP gnomAD v4 |
11 | g.22625389G>C | CA380059084 | FANCF | c.422C>G (p.Ser141Cys)
| dbSNP |
11 | g.22625389G= | CA1957607173 | FANCF | c.422C= (p.Ser141=)
| |
11 | g.22625389G>T | CA380059082 | FANCF | c.422C>A (p.Ser141Tyr)
| gnomAD v4 |
11 | g.22625390A= | CA1957607174 | FANCF | c.421T= (p.Ser141=)
| |
11 | g.22625390A>C | CA380059085 | FANCF | c.421T>G (p.Ser141Ala)
| dbSNP |
11 | g.22625390A>G | CA380059086 | FANCF | c.421T>C (p.Ser141Pro)
| |
11 | g.22625390A>T | CA380059087 | FANCF | c.421T>A (p.Ser141Thr)
| |
11 | g.22625391C>A | CA473533598 | FANCF | c.420G>T (p.Arg140=)
| |
11 | g.22625391C>G | CA473533599 | FANCF | c.420G>C (p.Arg140=)
| |
11 | g.22625391C>T | CA473533600 | FANCF | c.420G>A (p.Arg140=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625392C>A | CA380059088 | FANCF | c.419G>T (p.Arg140Leu)
| |
11 | g.22625392C= | CA1957607175 | FANCF | c.419G= (p.Arg140=)
| |
11 | g.22625392C>G | CA380059089 | FANCF | c.419G>C (p.Arg140Pro)
| dbSNP |
11 | g.22625392C>T | CA219086645 | FANCF | c.419G>A (p.Arg140Gln)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625393G>A | CA380059090 | FANCF | c.418C>T (p.Arg140Trp)
| dbSNP gnomAD v4 |
11 | g.22625393G>C | CA380059091 | FANCF | c.418C>G (p.Arg140Gly)
| |
11 | g.22625393G>T | CA473533604 | FANCF | c.418C>A (p.Arg140=)
| |
11 | g.22625394C>A | CA473533607 | FANCF | c.417G>T (p.Arg139=)
| |
11 | g.22625394C>G | CA473533606 | FANCF | c.417G>C (p.Arg139=)
| dbSNP |
11 | g.22625394C>T | CA473533605 | FANCF | c.417G>A (p.Arg139=)
| |
11 | g.22625395C>A | CA380059092 | FANCF | c.416G>T (p.Arg139Leu)
| |
11 | g.22625395C= | CA1957607176 | FANCF | c.416G= (p.Arg139=)
| |
11 | g.22625395C>G | CA380059093 | FANCF | c.416G>C (p.Arg139Pro)
| gnomAD v4 |
11 | g.22625395C>T | CA380059094 | FANCF | c.416G>A (p.Arg139Gln)
| dbSNP gnomAD v4 |
11 | g.22625396G>A | CA380059095 | FANCF | c.415C>T (p.Arg139Trp)
| gnomAD v4 |
11 | g.22625396G>C | CA5924337 | FANCF | c.415C>G (p.Arg139Gly)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625396G= | CA1957607177 | FANCF | c.415C= (p.Arg139=)
| |
11 | g.22625396G>T | CA473533609 | FANCF | c.415C>A (p.Arg139=)
| |
11 | g.22625403_22625411dup | CA5924336 | FANCF | c.407_415dup (p.Arg138_Arg139insLeuAlaArg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625397G>A | CA5924338 | FANCF | c.414C>T (p.Arg138=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625397G>C | CA473533611 | FANCF | c.414C>G (p.Arg138=)
| |
11 | g.22625397G= | CA1957607178 | FANCF | c.414C= (p.Arg138=)
| |
11 | g.22625397G>T | CA473533612 | FANCF | c.414C>A (p.Arg138=)
| |
11 | g.22625398C>A | CA380059097 | FANCF | c.413G>T (p.Arg138Leu)
| gnomAD v4 |
11 | g.22625398C= | CA1957607179 | FANCF | c.413G= (p.Arg138=)
| |
11 | g.22625398C>G | CA380059096 | FANCF | c.413G>C (p.Arg138Pro)
| dbSNP |
11 | g.22625398C>T | CA380059098 | FANCF | c.413G>A (p.Arg138His)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625399G>A | CA5924340 | FANCF | c.412C>T (p.Arg138Cys)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625399G>C | CA380059099 | FANCF | c.412C>G (p.Arg138Gly)
| |
11 | g.22625399G= | CA1957607180 | FANCF | c.412C= (p.Arg138=)
| |
11 | g.22625399G>T | CA5924339 | FANCF | c.412C>A (p.Arg138Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625400G>A | CA5924341 | FANCF | c.411C>T (p.Ala137=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625400G>C | CA473533614 | FANCF | c.411C>G (p.Ala137=)
| |
11 | g.22625400G= | CA1957607181 | FANCF | c.411C= (p.Ala137=)
| |
11 | g.22625400G>T | CA473533616 | FANCF | c.411C>A (p.Ala137=)
| |
11 | g.22625401G>A | CA380059101 | FANCF | c.410C>T (p.Ala137Val)
| dbSNP gnomAD v4 |
11 | g.22625401G>C | CA380059100 | FANCF | c.410C>G (p.Ala137Gly)
| |
11 | g.22625401G>T | CA380059102 | FANCF | c.410C>A (p.Ala137Asp)
| |
11 | g.22625402C>A | CA380059103 | FANCF | c.409G>T (p.Ala137Ser)
| |
11 | g.22625402C>G | CA380059105 | FANCF | c.409G>C (p.Ala137Pro)
| |
11 | g.22625402C>T | CA380059104 | FANCF | c.409G>A (p.Ala137Thr)
| dbSNP |
11 | g.22625403A= | CA1957607182 | FANCF | c.408T= (p.Leu136=)
| |
11 | g.22625403A>C | CA473533618 | FANCF | c.408T>G (p.Leu136=)
| |
11 | g.22625403A>G | CA473533619 | FANCF | c.408T>C (p.Leu136=)
| |
11 | g.22625403A>T | CA473533620 | FANCF | c.408T>A (p.Leu136=)
| |
11 | g.22625404A>C | CA380059106 | FANCF | c.407T>G (p.Leu136Arg)
| |
11 | g.22625404A>G | CA380059107 | FANCF | c.407T>C (p.Leu136Pro)
| dbSNP |
11 | g.22625404A>T | CA380059108 | FANCF | c.407T>A (p.Leu136His)
| |
11 | g.22625408_22625416dup | CA5924342 | FANCF | c.399_407dup (p.Leu136_Ala137insAlaArgLeu)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625408_22625416del | CA2612850471 | FANCF | c.399_407del (p.Ala134_Leu136del)
| gnomAD v4 |
11 | g.22625405G>A | CA380059109 | FANCF | c.406C>T (p.Leu136Phe)
| |
11 | g.22625405G>C | CA380059110 | FANCF | c.406C>G (p.Leu136Val)
| gnomAD v4 |
11 | g.22625405G>T | CA380059111 | FANCF | c.406C>A (p.Leu136Ile)
| |
11 | g.22625406G>A | CA473533624 | FANCF | c.405C>T (p.Arg135=)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625406G>C | CA473533625 | FANCF | c.405C>G (p.Arg135=)
| |
11 | g.22625406G= | CA1957607183 | FANCF | c.405C= (p.Arg135=)
| |
11 | g.22625406G>T | CA473533626 | FANCF | c.405C>A (p.Arg135=)
| |
11 | g.22625407C>A | CA5924343 | FANCF | c.404G>T (p.Arg135Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625407C= | CA1957607184 | FANCF | c.404G= (p.Arg135=)
| |
11 | g.22625407C>G | CA380059112 | FANCF | c.404G>C (p.Arg135Pro)
| dbSNP |
11 | g.22625407C>T | CA380059113 | FANCF | c.404G>A (p.Arg135His)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625408G>A | CA380059116 | FANCF | c.403C>T (p.Arg135Cys)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625408G>C | CA380059115 | FANCF | c.403C>G (p.Arg135Gly)
| |
11 | g.22625408G>T | CA380059114 | FANCF | c.403C>A (p.Arg135Ser)
| |
11 | g.22625409G>A | CA5924344 | FANCF | c.402C>T (p.Ala134=)
| dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
11 | g.22625409G>C | CA473533629 | FANCF | c.402C>G (p.Ala134=)
| |
11 | g.22625409G= | CA1957607185 | FANCF | c.402C= (p.Ala134=)
| |
11 | g.22625409G>T | CA473533628 | FANCF | c.402C>A (p.Ala134=)
| |
11 | g.22625410G>A | CA380059117 | FANCF | c.401C>T (p.Ala134Val)
| dbSNP |
11 | g.22625410G>C | CA380059118 | FANCF | c.401C>G (p.Ala134Gly)
| gnomAD v4 |
11 | g.22625410G>T | CA380059119 | FANCF | c.401C>A (p.Ala134Asp)
| |
11 | g.22625411C>A | CA380059120 | FANCF | c.400G>T (p.Ala134Ser)
| |
11 | g.22625411C>G | CA380059121 | FANCF | c.400G>C (p.Ala134Pro)
| |
11 | g.22625411C>T | CA380059122 | FANCF | c.400G>A (p.Ala134Thr)
| dbSNP |
11 | g.22625412C>A | CA473533630 | FANCF | c.399G>T (p.Leu133=)
| COSMIC |
11 | g.22625412C>G | CA473533631 | FANCF | c.399G>C (p.Leu133=)
| |
11 | g.22625412C>T | CA473533633 | FANCF | c.399G>A (p.Leu133=)
| |
11 | g.22625413A>C | CA380059123 | FANCF | c.398T>G (p.Leu133Arg)
| |
11 | g.22625413A>G | CA380059124 | FANCF | c.398T>C (p.Leu133Pro)
| |
11 | g.22625413A>T | CA380059125 | FANCF | c.398T>A (p.Leu133Gln)
| |
11 | g.22625413_22625460delinsAGGCTCTCTTGGAGTGTCTCCTCATCGGCGTCCCGGACGCCCGGGCCG | CA1957607186 | FANCF | c.351_398delinsCGGCCCGGGCGTCCGGGACGCCGATGAGGAGACACTCCAAGAGAGCCT (p.Pro117=)
| |
11 | g.22625414G>A | CA473533634 | FANCF | c.397C>T (p.Leu133=)
| gnomAD v4 |
11 | g.22625414G>C | CA380059126 | FANCF | c.397C>G (p.Leu133Val)
| |
11 | g.22625414G>T | CA380059127 | FANCF | c.397C>A (p.Leu133Met)
| |
11 | g.22625416_22625462del | CA253843 | FANCF | c.351_397del (p.Gly120ProfsTer17)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |