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 |
11 | g.22625415G>A | CA473533635 | FANCF | c.396C>T (p.Ser132=)
| dbSNP |
11 | g.22625415G>C | CA380059128 | FANCF | c.396C>G (p.Ser132Arg)
| |
11 | g.22625415G>T | CA380059129 | FANCF | c.396C>A (p.Ser132Arg)
| gnomAD v4 |
11 | g.22625416C>A | CA380059130 | FANCF | c.395G>T (p.Ser132Ile)
| dbSNP COSMIC |
11 | g.22625416C>G | CA380059131 | FANCF | c.395G>C (p.Ser132Thr)
| |
11 | g.22625416C>T | CA380059132 | FANCF | c.395G>A (p.Ser132Asn)
| |
11 | g.22625417_22625454del | CA2695213428 | FANCF | c.358_395del (p.Gly120ProfsTer20)
| |
11 | g.22625417T>A | CA380059133 | FANCF | c.394A>T (p.Ser132Cys)
| |
11 | g.22625417T>C | CA380059134 | FANCF | c.394A>G (p.Ser132Gly)
| ClinVar dbSNP |
11 | g.22625417T>G | CA380059135 | FANCF | c.394A>C (p.Ser132Arg)
| |
11 | g.22625418C>A | CA380059136 | FANCF | c.393G>T (p.Glu131Asp)
| |
11 | g.22625418C>G | CA380059137 | FANCF | c.393G>C (p.Glu131Asp)
| |
11 | g.22625418C>T | CA473533638 | FANCF | c.393G>A (p.Glu131=)
| gnomAD v4 |
11 | g.22625419T>A | CA380059140 | FANCF | c.392A>T (p.Glu131Val)
| |
11 | g.22625419T>C | CA380059139 | FANCF | c.392A>G (p.Glu131Gly)
| |
11 | g.22625419T>G | CA380059138 | FANCF | c.392A>C (p.Glu131Ala)
| |
11 | g.22625420C>A | CA380059141 | FANCF | c.391G>T (p.Glu131Ter)
| |
11 | g.22625420C>G | CA380059142 | FANCF | c.391G>C (p.Glu131Gln)
| dbSNP |
11 | g.22625420C>T | CA380059143 | FANCF | c.391G>A (p.Glu131Lys)
| ClinVar gnomAD v4 |
11 | g.22625421T>A | CA380059144 | FANCF | c.390A>T (p.Gln130His)
| |
11 | g.22625421T>C | CA5924345 | FANCF | c.390A>G (p.Gln130=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625421T>G | CA380059145 | FANCF | c.390A>C (p.Gln130His)
| |
11 | g.22625421T= | CA1957607187 | FANCF | c.390A= (p.Gln130=)
| |
11 | g.22625422T>A | CA5924346 | FANCF | c.389A>T (p.Gln130Leu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625422T>C | CA5924347 | FANCF | c.389A>G (p.Gln130Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625422T>G | CA380059146 | FANCF | c.389A>C (p.Gln130Pro)
| |
11 | g.22625422T= | CA1957607188 | FANCF | c.389A= (p.Gln130=)
| |
11 | g.22625423G>A | CA380059147 | FANCF | c.388C>T (p.Gln130Ter)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625423G>C | CA380059148 | FANCF | c.388C>G (p.Gln130Glu)
| ClinVar |
11 | g.22625423G= | CA1957607189 | FANCF | c.388C= (p.Gln130=)
| |
11 | g.22625423G>T | CA5924348 | FANCF | c.388C>A (p.Gln130Lys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625424dup | CA2521117772 | FANCF | c.388dup (p.Gln130ProfsTer23)
| ClinVar gnomAD v4 |
11 | g.22625424G>A | CA5924349 | FANCF | c.387C>T (p.Leu129=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625424G>C | CA473533643 | FANCF | c.387C>G (p.Leu129=)
| |
11 | g.22625424G= | CA1957607190 | FANCF | c.387C= (p.Leu129=)
| |
11 | g.22625424G>T | CA473533644 | FANCF | c.387C>A (p.Leu129=)
| |
11 | g.22625425A= | CA1957607191 | FANCF | c.386T= (p.Leu129=)
| |
11 | g.22625425A>C | CA5924350 | FANCF | c.386T>G (p.Leu129Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625425A>G | CA380059150 | FANCF | c.386T>C (p.Leu129Pro)
| |
11 | g.22625425A>T | CA380059149 | FANCF | c.386T>A (p.Leu129His)
| |
11 | g.22625426G>A | CA380059151 | FANCF | c.385C>T (p.Leu129Phe)
| |
11 | g.22625426G>C | CA159566 | FANCF | c.385C>G (p.Leu129Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625426G= | CA1957607192 | FANCF | c.385C= (p.Leu129=)
| |
11 | g.22625426G>T | CA380059152 | FANCF | c.385C>A (p.Leu129Ile)
| ClinVar |
11 | g.22625427T>A | CA473533645 | FANCF | c.384A>T (p.Thr128=)
| |
11 | g.22625427T>C | CA5924352 | FANCF | c.384A>G (p.Thr128=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625427T>G | CA5924351 | FANCF | c.384A>C (p.Thr128=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625427T= | CA1957607193 | FANCF | c.384A= (p.Thr128=)
| |
11 | g.22625428G>A | CA380059155 | FANCF | c.383C>T (p.Thr128Ile)
| dbSNP gnomAD v4 |
11 | g.22625428G>C | CA380059153 | FANCF | c.383C>G (p.Thr128Arg)
| |
11 | g.22625428G= | CA1957607194 | FANCF | c.383C= (p.Thr128=)
| |
11 | g.22625428G>T | CA380059154 | FANCF | c.383C>A (p.Thr128Lys)
| |
11 | g.22625429T>A | CA380059156 | FANCF | c.382A>T (p.Thr128Ser)
| dbSNP |
11 | g.22625429T>C | CA380059157 | FANCF | c.382A>G (p.Thr128Ala)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625429T>G | CA380059158 | FANCF | c.382A>C (p.Thr128Pro)
| |
11 | g.22625429T= | CA1957607195 | FANCF | c.382A= (p.Thr128=)
| |
11 | g.22625430C>A | CA380059159 | FANCF | c.381G>T (p.Glu127Asp)
| |
11 | g.22625430C>G | CA380059160 | FANCF | c.381G>C (p.Glu127Asp)
| |
11 | g.22625430C>T | CA473533649 | FANCF | c.381G>A (p.Glu127=)
| |
11 | g.22625433_22625435del | CA2790714010 | FANCF | c.379_381del (p.Glu127del)
| |
11 | g.22625431T>A | CA380059163 | FANCF | c.380A>T (p.Glu127Val)
| |
11 | g.22625431T>C | CA380059161 | FANCF | c.380A>G (p.Glu127Gly)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625431T>G | CA380059162 | FANCF | c.380A>C (p.Glu127Ala)
| |
11 | g.22625431T= | CA1957607196 | FANCF | c.380A= (p.Glu127=)
| |
11 | g.22625432C>A | CA380059164 | FANCF | c.379G>T (p.Glu127Ter)
| |
11 | g.22625432C= | CA1957607197 | FANCF | c.379G= (p.Glu127=)
| |
11 | g.22625432C>G | CA380059165 | FANCF | c.379G>C (p.Glu127Gln)
| |
11 | g.22625432C>T | CA380059166 | FANCF | c.379G>A (p.Glu127Lys)
| dbSNP gnomAD v2 |
11 | g.22625433C>A | CA380059167 | FANCF | c.378G>T (p.Glu126Asp)
| |
11 | g.22625433C= | CA1957607198 | FANCF | c.378G= (p.Glu126=)
| |
11 | g.22625433C>G | CA380059168 | FANCF | c.378G>C (p.Glu126Asp)
| |
11 | g.22625433C>T | CA473533651 | FANCF | c.378G>A (p.Glu126=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625434T>A | CA380059169 | FANCF | c.377A>T (p.Glu126Val)
| |
11 | g.22625434T>C | CA380059170 | FANCF | c.377A>G (p.Glu126Gly)
| |
11 | g.22625434T>G | CA380059171 | FANCF | c.377A>C (p.Glu126Ala)
| |
11 | g.22625435C>A | CA380059172 | FANCF | c.376G>T (p.Glu126Ter)
| |
11 | g.22625435C>G | CA380059173 | FANCF | c.376G>C (p.Glu126Gln)
| |
11 | g.22625435C>T | CA380059174 | FANCF | c.376G>A (p.Glu126Lys)
| dbSNP |
11 | g.22625436A= | CA1957607199 | FANCF | c.375T= (p.Asp125=)
| |
11 | g.22625436A>C | CA380059175 | FANCF | c.375T>G (p.Asp125Glu)
| |
11 | g.22625436A>G | CA473533654 | FANCF | c.375T>C (p.Asp125=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625436A>T | CA380059176 | FANCF | c.375T>A (p.Asp125Glu)
| |
11 | g.22625437T>A | CA380059177 | FANCF | c.374A>T (p.Asp125Val)
| |
11 | g.22625437T>C | CA380059180 | FANCF | c.374A>G (p.Asp125Gly)
| dbSNP |
11 | g.22625437T>G | CA380059178 | FANCF | c.374A>C (p.Asp125Ala)
| |
11 | g.22625437T= | CA1957607200 | FANCF | c.374A= (p.Asp125=)
| |
11 | g.22625438C>A | CA380059182 | FANCF | c.373G>T (p.Asp125Tyr)
| dbSNP |
11 | g.22625438C= | CA1957607201 | FANCF | c.373G= (p.Asp125=)
| |
11 | g.22625438C>G | CA380059183 | FANCF | c.373G>C (p.Asp125His)
| |
11 | g.22625438C>T | CA159581 | FANCF | c.373G>A (p.Asp125Asn)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625439G>A | CA473533656 | FANCF | c.372C>T (p.Ala124=)
| |
11 | g.22625439G>C | CA5924353 | FANCF | c.372C>G (p.Ala124=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625439G= | CA1957607202 | FANCF | c.372C= (p.Ala124=)
| |
11 | g.22625439G>T | CA5924354 | FANCF | c.372C>A (p.Ala124=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |