11 | g.22624967C>A | CA380058216 | FANCF | c.844G>T (p.Gly282Cys)
| |
11 | g.22624967C= | CA1957606942 | FANCF | c.844G= (p.Gly282=)
| |
11 | g.22624967C>G | CA380058217 | FANCF | c.844G>C (p.Gly282Arg)
| dbSNP gnomAD v2 |
11 | g.22624967C>T | CA380058218 | FANCF | c.844G>A (p.Gly282Ser)
| |
11 | g.22624968C>A | CA380058219 | FANCF | c.843G>T (p.Trp281Cys)
| |
11 | g.22624968C>G | CA380058220 | FANCF | c.843G>C (p.Trp281Cys)
| |
11 | g.22624968C>T | CA380058221 | FANCF | c.843G>A (p.Trp281Ter)
| |
11 | g.22624969C>A | CA380058222 | FANCF | c.842G>T (p.Trp281Leu)
| |
11 | g.22624969C= | CA1957606943 | FANCF | c.842G= (p.Trp281=)
| |
11 | g.22624969C>G | CA380058223 | FANCF | c.842G>C (p.Trp281Ser)
| |
11 | g.22624969C>T | CA380058224 | FANCF | c.842G>A (p.Trp281Ter)
| dbSNP gnomAD v2 |
11 | g.22624970A= | CA1957606944 | FANCF | c.841T= (p.Trp281=)
| |
11 | g.22624970A>C | CA380058227 | FANCF | c.841T>G (p.Trp281Gly)
| dbSNP |
11 | g.22624970A>G | CA380058226 | FANCF | c.841T>C (p.Trp281Arg)
| ClinVar dbSNP |
11 | g.22624970A>T | CA380058225 | FANCF | c.841T>A (p.Trp281Arg)
| |
11 | g.22624971G>A | CA473533430 | FANCF | c.840C>T (p.Asp280=)
| dbSNP gnomAD v4 COSMIC |
11 | g.22624971G>C | CA380058228 | FANCF | c.840C>G (p.Asp280Glu)
| |
11 | g.22624971G= | CA1957606945 | FANCF | c.840C= (p.Asp280=)
| |
11 | g.22624971G>T | CA380058229 | FANCF | c.840C>A (p.Asp280Glu)
| |
11 | g.22624972T>A | CA380058230 | FANCF | c.839A>T (p.Asp280Val)
| |
11 | g.22624972T>C | CA219086615 | FANCF | c.839A>G (p.Asp280Gly)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22624972T>G | CA380058231 | FANCF | c.839A>C (p.Asp280Ala)
| |
11 | g.22624972T= | CA1957606946 | FANCF | c.839A= (p.Asp280=)
| |
11 | g.22624973C>A | CA380058232 | FANCF | c.838G>T (p.Asp280Tyr)
| ClinVar dbSNP |
11 | g.22624973C= | CA1957606947 | FANCF | c.838G= (p.Asp280=)
| |
11 | g.22624973C>G | CA380058233 | FANCF | c.838G>C (p.Asp280His)
| |
11 | g.22624973C>T | CA380058234 | FANCF | c.838G>A (p.Asp280Asn)
| ClinVar dbSNP |
11 | g.22624974T>A | CA473533431 | FANCF | c.837A>T (p.Thr279=)
| |
11 | g.22624974T>C | CA5924249 | FANCF | c.837A>G (p.Thr279=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22624974T>G | CA473533432 | FANCF | c.837A>C (p.Thr279=)
| |
11 | g.22624974T= | CA1957606948 | FANCF | c.837A= (p.Thr279=)
| |
11 | g.22624975G>A | CA380058235 | FANCF | c.836C>T (p.Thr279Ile)
| dbSNP gnomAD v4 |
11 | g.22624975G>C | CA380058236 | FANCF | c.836C>G (p.Thr279Arg)
| |
11 | g.22624975G>T | CA380058237 | FANCF | c.836C>A (p.Thr279Lys)
| |
11 | g.22624976T>A | CA380058240 | FANCF | c.835A>T (p.Thr279Ser)
| |
11 | g.22624976T>C | CA380058239 | FANCF | c.835A>G (p.Thr279Ala)
| |
11 | g.22624976T>G | CA380058238 | FANCF | c.835A>C (p.Thr279Pro)
| |
11 | g.22624977T>A | CA473533433 | FANCF | c.834A>T (p.Leu278=)
| |
11 | g.22624977T>C | CA473533434 | FANCF | c.834A>G (p.Leu278=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22624977T>G | CA473533435 | FANCF | c.834A>C (p.Leu278=)
| |
11 | g.22624977T= | CA1957606949 | FANCF | c.834A= (p.Leu278=)
| |
11 | g.22624978A>C | CA380058241 | FANCF | c.833T>G (p.Leu278Arg)
| |
11 | g.22624978A>G | CA380058242 | FANCF | c.833T>C (p.Leu278Pro)
| |
11 | g.22624978A>T | CA380058243 | FANCF | c.833T>A (p.Leu278Gln)
| |
11 | g.22624979G>A | CA473533436 | FANCF | c.832C>T (p.Leu278=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22624979G>C | CA380058244 | FANCF | c.832C>G (p.Leu278Val)
| |
11 | g.22624979G= | CA1957606950 | FANCF | c.832C= (p.Leu278=)
| |
11 | g.22624979G>T | CA380058245 | FANCF | c.832C>A (p.Leu278Ile)
| |
11 | g.22624980C>A | CA473533437 | FANCF | c.831G>T (p.Leu277=)
| gnomAD v4 |
11 | g.22624980C= | CA1957606951 | FANCF | c.831G= (p.Leu277=)
| |
11 | g.22624980C>G | CA473533438 | FANCF | c.831G>C (p.Leu277=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22624980C>T | CA473533439 | FANCF | c.831G>A (p.Leu277=)
| dbSNP |
11 | g.22624981A>C | CA380058246 | FANCF | c.830T>G (p.Leu277Arg)
| gnomAD v4 |
11 | g.22624981A>G | CA380058247 | FANCF | c.830T>C (p.Leu277Pro)
| gnomAD v4 |
11 | g.22624981A>T | CA380058248 | FANCF | c.830T>A (p.Leu277Gln)
| |
11 | g.22624982G>A | CA473533440 | FANCF | c.829C>T (p.Leu277=)
| dbSNP gnomAD v4 |
11 | g.22624982G>C | CA380058249 | FANCF | c.829C>G (p.Leu277Val)
| ClinVar COSMIC |
11 | g.22624982G>T | CA380058250 | FANCF | c.829C>A (p.Leu277Met)
| |
11 | g.22624983A>C | CA473533441 | FANCF | c.828T>G (p.Gly276=)
| |
11 | g.22624983A>G | CA473533442 | FANCF | c.828T>C (p.Gly276=)
| |
11 | g.22624983A>T | CA473533443 | FANCF | c.828T>A (p.Gly276=)
| |
11 | g.22624984C>A | CA380058251 | FANCF | c.827G>T (p.Gly276Val)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22624984C= | CA1957606952 | FANCF | c.827G= (p.Gly276=)
| |
11 | g.22624984C>G | CA380058252 | FANCF | c.827G>C (p.Gly276Ala)
| |
11 | g.22624984C>T | CA380058253 | FANCF | c.827G>A (p.Gly276Asp)
| dbSNP |
11 | g.22624985C>A | CA380058256 | FANCF | c.826G>T (p.Gly276Cys)
| gnomAD v4 |
11 | g.22624985C>G | CA380058255 | FANCF | c.826G>C (p.Gly276Arg)
| |
11 | g.22624985C>T | CA380058254 | FANCF | c.826G>A (p.Gly276Ser)
| dbSNP |
11 | g.22624986C>A | CA473533444 | FANCF | c.825G>T (p.Leu275=)
| |
11 | g.22624986C= | CA1957606953 | FANCF | c.825G= (p.Leu275=)
| |
11 | g.22624986C>G | CA473533445 | FANCF | c.825G>C (p.Leu275=)
| |
11 | g.22624986C>T | CA5924250 | FANCF | c.825G>A (p.Leu275=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22624987A= | CA1957606954 | FANCF | c.824T= (p.Leu275=)
| |
11 | g.22624987A>C | CA380058257 | FANCF | c.824T>G (p.Leu275Arg)
| |
11 | g.22624987A>G | CA5924251 | FANCF | c.824T>C (p.Leu275Pro)
| dbSNP ExAC gnomAD v2 |
11 | g.22624987A>T | CA380058258 | FANCF | c.824T>A (p.Leu275Gln)
| |
11 | g.22624988G>A | CA473533446 | FANCF | c.823C>T (p.Leu275=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22624988G>C | CA380058259 | FANCF | c.823C>G (p.Leu275Val)
| dbSNP gnomAD v4 |
11 | g.22624988G= | CA1957606955 | FANCF | c.823C= (p.Leu275=)
| |
11 | g.22624988G>T | CA380058260 | FANCF | c.823C>A (p.Leu275Met)
| |
11 | g.22624989A= | CA1957606956 | FANCF | c.822T= (p.Tyr274=)
| |
11 | g.22624989A>C | CA380058261 | FANCF | c.822T>G (p.Tyr274Ter)
| |
11 | g.22624989A>G | CA5924252 | FANCF | c.822T>C (p.Tyr274=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22624989A>T | CA380058262 | FANCF | c.822T>A (p.Tyr274Ter)
| |
11 | g.22624990T>A | CA380058263 | FANCF | c.821A>T (p.Tyr274Phe)
| |
11 | g.22624990T>C | CA5924253 | FANCF | c.821A>G (p.Tyr274Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22624990T>G | CA5924254 | FANCF | c.821A>C (p.Tyr274Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22624990T= | CA1957606957 | FANCF | c.821A= (p.Tyr274=)
| |
11 | g.22624990_22624994delinsTAGAC | CA1957606958 | FANCF | c.817_821delinsGTCTA (p.Val273=)
| |
11 | g.22624991A>C | CA380058264 | FANCF | c.820T>G (p.Tyr274Asp)
| |
11 | g.22624991A>G | CA380058265 | FANCF | c.820T>C (p.Tyr274His)
| |
11 | g.22624991A>T | CA380058266 | FANCF | c.820T>A (p.Tyr274Asn)
| |
11 | g.22624991dup | CA2612850459 | FANCF | c.820dup (p.Tyr274LeufsTer15)
| gnomAD v4 |
11 | g.22624993_22624996del | CA1957606959 | FANCF | c.817_820del (p.Val273IlefsTer5)
| ClinVar dbSNP gnomAD v4 |
11 | g.22624992del | CA2612850460 | FANCF | c.819del (p.Tyr274IlefsTer5)
| gnomAD v4 |
11 | g.22624992G>A | CA473533447 | FANCF | c.819C>T (p.Val273=)
| gnomAD v4 |
11 | g.22624992G>C | CA473533449 | FANCF | c.819C>G (p.Val273=)
| |
11 | g.22624992G>T | CA473533448 | FANCF | c.819C>A (p.Val273=)
| |
11 | g.22624993A>C | CA380058269 | FANCF | c.818T>G (p.Val273Gly)
| COSMIC |
11 | g.22624993A>G | CA380058268 | FANCF | c.818T>C (p.Val273Ala)
| |
11 | g.22624993A>T | CA380058267 | FANCF | c.818T>A (p.Val273Asp)
| |
11 | g.22624994C>A | CA380058270 | FANCF | c.817G>T (p.Val273Phe)
| |
11 | g.22624994C= | CA1957606960 | FANCF | c.817G= (p.Val273=)
| |
11 | g.22624994C>G | CA380058271 | FANCF | c.817G>C (p.Val273Leu)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.22624994C>T | CA380058272 | FANCF | c.817G>A (p.Val273Ile)
| |
11 | g.22624995A>C | CA473533450 | FANCF | c.816T>G (p.Pro272=)
| |
11 | g.22624995A>G | CA473533451 | FANCF | c.816T>C (p.Pro272=)
| gnomAD v4 |
11 | g.22624995A>T | CA473533452 | FANCF | c.816T>A (p.Pro272=)
| |
11 | g.22624996G>A | CA219086616 | FANCF | c.815C>T (p.Pro272Leu)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22624996G>C | CA380058273 | FANCF | c.815C>G (p.Pro272Arg)
| dbSNP |
11 | g.22624996G= | CA1957606961 | FANCF | c.815C= (p.Pro272=)
| |
11 | g.22624996G>T | CA380058274 | FANCF | c.815C>A (p.Pro272His)
| |
11 | g.22624997G>A | CA380058275 | FANCF | c.814C>T (p.Pro272Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.22624997G>C | CA5924255 | FANCF | c.814C>G (p.Pro272Ala)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22624997G= | CA1957606962 | FANCF | c.814C= (p.Pro272=)
| |
11 | g.22624997G>T | CA380058276 | FANCF | c.814C>A (p.Pro272Thr)
| |
11 | g.22624998A>C | CA473533453 | FANCF | c.813T>G (p.Ser271=)
| |
11 | g.22624998A>G | CA473533454 | FANCF | c.813T>C (p.Ser271=)
| |
11 | g.22624998A>T | CA473533455 | FANCF | c.813T>A (p.Ser271=)
| |
11 | g.22624999G>A | CA380058277 | FANCF | c.812C>T (p.Ser271Phe)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22624999G>C | CA380058278 | FANCF | c.812C>G (p.Ser271Cys)
| |
11 | g.22624999G= | CA1957606963 | FANCF | c.812C= (p.Ser271=)
| |
11 | g.22624999G>T | CA380058279 | FANCF | c.812C>A (p.Ser271Tyr)
| |
11 | g.22625000A>C | CA380058282 | FANCF | c.811T>G (p.Ser271Ala)
| |
11 | g.22625000A>G | CA380058281 | FANCF | c.811T>C (p.Ser271Pro)
| |
11 | g.22625000A>T | CA380058280 | FANCF | c.811T>A (p.Ser271Thr)
| gnomAD v4 |
11 | g.22625001C>A | CA473533456 | FANCF | c.810G>T (p.Leu270=)
| dbSNP |
11 | g.22625001C= | CA1957606964 | FANCF | c.810G= (p.Leu270=)
| |
11 | g.22625001C>G | CA473533457 | FANCF | c.810G>C (p.Leu270=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625001C>T | CA473533458 | FANCF | c.810G>A (p.Leu270=)
| dbSNP |
11 | g.22625002A>C | CA380058285 | FANCF | c.809T>G (p.Leu270Arg)
| |
11 | g.22625002A>G | CA380058286 | FANCF | c.809T>C (p.Leu270Pro)
| |
11 | g.22625002A>T | CA380058287 | FANCF | c.809T>A (p.Leu270Gln)
| gnomAD v4 |
11 | g.22625003G>A | CA473533535 | FANCF | c.808C>T (p.Leu270=)
| dbSNP gnomAD v4 |
11 | g.22625003G>C | CA380058288 | FANCF | c.808C>G (p.Leu270Val)
| COSMIC |
11 | g.22625003G>T | CA380058289 | FANCF | c.808C>A (p.Leu270Met)
| gnomAD v4 |
11 | g.22625004C>A | CA473533537 | FANCF | c.807G>T (p.Ala269=)
| |
11 | g.22625004C= | CA1957606965 | FANCF | c.807G= (p.Ala269=)
| |
11 | g.22625004C>G | CA473533538 | FANCF | c.807G>C (p.Ala269=)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625004C>T | CA5924256 | FANCF | c.807G>A (p.Ala269=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.22625005G>A | CA380058290 | FANCF | c.806C>T (p.Ala269Val)
| dbSNP gnomAD v4 |
11 | g.22625005G>C | CA219086617 | FANCF | c.806C>G (p.Ala269Gly)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625005G= | CA1957606966 | FANCF | c.806C= (p.Ala269=)
| |
11 | g.22625005G>T | CA380058291 | FANCF | c.806C>A (p.Ala269Glu)
| |
11 | g.22625006C>A | CA380058292 | FANCF | c.805G>T (p.Ala269Ser)
| |
11 | g.22625006C>G | CA380058293 | FANCF | c.805G>C (p.Ala269Pro)
| |
11 | g.22625006C>T | CA380058294 | FANCF | c.805G>A (p.Ala269Thr)
| |
11 | g.22625007T>A | CA473533540 | FANCF | c.804A>T (p.Pro268=)
| |
11 | g.22625007T>C | CA473533542 | FANCF | c.804A>G (p.Pro268=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625007T>G | CA473533543 | FANCF | c.804A>C (p.Pro268=)
| |
11 | g.22625007T= | CA1957606967 | FANCF | c.804A= (p.Pro268=)
| |
11 | g.22625008G>A | CA380058296 | FANCF | c.803C>T (p.Pro268Leu)
| dbSNP gnomAD v4 |
11 | g.22625008G>C | CA380058297 | FANCF | c.803C>G (p.Pro268Arg)
| |
11 | g.22625008G>T | CA380058295 | FANCF | c.803C>A (p.Pro268Gln)
| |
11 | g.22625009G>A | CA380058298 | FANCF | c.802C>T (p.Pro268Ser)
| dbSNP |
11 | g.22625009G>C | CA380058299 | FANCF | c.802C>G (p.Pro268Ala)
| dbSNP gnomAD v4 |
11 | g.22625009G= | CA1957606968 | FANCF | c.802C= (p.Pro268=)
| |
11 | g.22625009G>T | CA380058300 | FANCF | c.802C>A (p.Pro268Thr)
| |
11 | g.22625010G>A | CA473533546 | FANCF | c.801C>T (p.His267=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625010G>C | CA5924257 | FANCF | c.801C>G (p.His267Gln)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625010G= | CA1957606969 | FANCF | c.801C= (p.His267=)
| |
11 | g.22625010G>T | CA5924258 | FANCF | c.801C>A (p.His267Gln)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625011T>A | CA380058303 | FANCF | c.800A>T (p.His267Leu)
| gnomAD v4 |
11 | g.22625011T>C | CA380058301 | FANCF | c.800A>G (p.His267Arg)
| |
11 | g.22625011T>G | CA380058302 | FANCF | c.800A>C (p.His267Pro)
| |
11 | g.22625012G>A | CA380058304 | FANCF | c.799C>T (p.His267Tyr)
| ClinVar dbSNP |
11 | g.22625012G>C | CA380058305 | FANCF | c.799C>G (p.His267Asp)
| |
11 | g.22625012G>T | CA380058306 | FANCF | c.799C>A (p.His267Asn)
| |
11 | g.22625013G>A | CA473533550 | FANCF | c.798C>T (p.Arg266=)
| |
11 | g.22625013G>C | CA473533549 | FANCF | c.798C>G (p.Arg266=)
| |
11 | g.22625013G>T | CA473533548 | FANCF | c.798C>A (p.Arg266=)
| |
11 | g.22625014C>A | CA380058307 | FANCF | c.797G>T (p.Arg266Leu)
| dbSNP |
11 | g.22625014C= | CA1957606970 | FANCF | c.797G= (p.Arg266=)
| |
11 | g.22625014C>G | CA380058308 | FANCF | c.797G>C (p.Arg266Pro)
| dbSNP |
11 | g.22625014C>T | CA219086618 | FANCF | c.797G>A (p.Arg266His)
| dbSNP gnomAD v4 |
11 | g.22625015G>A | CA5924259 | FANCF | c.796C>T (p.Arg266Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625015G>C | CA380058310 | FANCF | c.796C>G (p.Arg266Gly)
| |
11 | g.22625015G= | CA1957606971 | FANCF | c.796C= (p.Arg266=)
| |
11 | g.22625015G>T | CA380058309 | FANCF | c.796C>A (p.Arg266Ser)
| |
11 | g.22625016del | CA2612850461 | FANCF | c.796del (p.Arg266AlafsTer13)
| gnomAD v4 |
11 | g.22625016G>A | CA473533553 | FANCF | c.795C>T (p.Ser265=)
| dbSNP gnomAD v4 |
11 | g.22625016G>C | CA380058311 | FANCF | c.795C>G (p.Ser265Arg)
| |
11 | g.22625016G= | CA1957606972 | FANCF | c.795C= (p.Ser265=)
| |
11 | g.22625016G>T | CA5924260 | FANCF | c.795C>A (p.Ser265Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625017C>A | CA380058312 | FANCF | c.794G>T (p.Ser265Ile)
| |
11 | g.22625017C= | CA1957606973 | FANCF | c.794G= (p.Ser265=)
| |
11 | g.22625017C>G | CA380058313 | FANCF | c.794G>C (p.Ser265Thr)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625017C>T | CA380058314 | FANCF | c.794G>A (p.Ser265Asn)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625018T>A | CA380058315 | FANCF | c.793A>T (p.Ser265Cys)
| |
11 | g.22625018T>C | CA380058316 | FANCF | c.793A>G (p.Ser265Gly)
| |
11 | g.22625018T>G | CA380058317 | FANCF | c.793A>C (p.Ser265Arg)
| |
11 | g.22625019A>C | CA473533556 | FANCF | c.792T>G (p.Thr264=)
| |
11 | g.22625019A>G | CA473533558 | FANCF | c.792T>C (p.Thr264=)
| COSMIC |
11 | g.22625019A>T | CA473533557 | FANCF | c.792T>A (p.Thr264=)
| gnomAD v4 |
11 | g.22625019dup | CA2695201107 | FANCF | c.792dup (p.Ser265Ter)
| ClinVar |
11 | g.22625020G>A | CA380058320 | FANCF | c.791C>T (p.Thr264Ile)
| dbSNP gnomAD v4 |
11 | g.22625020G>C | CA380058319 | FANCF | c.791C>G (p.Thr264Ser)
| |
11 | g.22625020G= | CA1957606974 | FANCF | c.791C= (p.Thr264=)
| |
11 | g.22625020G>T | CA380058318 | FANCF | c.791C>A (p.Thr264Asn)
| |
11 | g.22625021T>A | CA380058321 | FANCF | c.790A>T (p.Thr264Ser)
| ClinVar dbSNP |
11 | g.22625021T>C | CA380058322 | FANCF | c.790A>G (p.Thr264Ala)
| dbSNP gnomAD v4 |
11 | g.22625021T>G | CA380058323 | FANCF | c.790A>C (p.Thr264Pro)
| |
11 | g.22625021T= | CA1957606975 | FANCF | c.790A= (p.Thr264=)
| |
11 | g.22625022C>A | CA473533562 | FANCF | c.789G>T (p.Val263=)
| |
11 | g.22625022C= | CA1957606976 | FANCF | c.789G= (p.Val263=)
| |
11 | g.22625022C>G | CA473533563 | FANCF | c.789G>C (p.Val263=)
| gnomAD v4 |
11 | g.22625022C>T | CA473533564 | FANCF | c.789G>A (p.Val263=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625023A>C | CA380058324 | FANCF | c.788T>G (p.Val263Gly)
| |
11 | g.22625023A>G | CA380058325 | FANCF | c.788T>C (p.Val263Ala)
| |
11 | g.22625023A>T | CA380058326 | FANCF | c.788T>A (p.Val263Glu)
| |
11 | g.22625024C>A | CA380058327 | FANCF | c.787G>T (p.Val263Leu)
| |
11 | g.22625024C= | CA1957606977 | FANCF | c.787G= (p.Val263=)
| |
11 | g.22625024C>G | CA380058329 | FANCF | c.787G>C (p.Val263Leu)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625024C>T | CA380058328 | FANCF | c.787G>A (p.Val263Met)
| |
11 | g.22625025T>A | CA380058330 | FANCF | c.786A>T (p.Leu262Phe)
| |
11 | g.22625025T>C | CA5924261 | FANCF | c.786A>G (p.Leu262=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625025T>G | CA380058331 | FANCF | c.786A>C (p.Leu262Phe)
| |
11 | g.22625025T= | CA1957606978 | FANCF | c.786A= (p.Leu262=)
| |
11 | g.22625026A= | CA1957606979 | FANCF | c.785T= (p.Leu262=)
| |
11 | g.22625026A>C | CA219086619 | FANCF | c.785T>G (p.Leu262Ter)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625026A>G | CA5924262 | FANCF | c.785T>C (p.Leu262Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625026A>T | CA380058332 | FANCF | c.785T>A (p.Leu262Ter)
| |
11 | g.22625027A= | CA1957606980 | FANCF | c.784T= (p.Leu262=)
| |
11 | g.22625027A>C | CA380058333 | FANCF | c.784T>G (p.Leu262Val)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625027A>G | CA473533569 | FANCF | c.784T>C (p.Leu262=)
| |
11 | g.22625027A>T | CA380058334 | FANCF | c.784T>A (p.Leu262Ile)
| |
11 | g.22625028A>C | CA473533571 | FANCF | c.783T>G (p.Thr261=)
| |
11 | g.22625028A>G | CA473533572 | FANCF | c.783T>C (p.Thr261=)
| |
11 | g.22625028A>T | CA473533573 | FANCF | c.783T>A (p.Thr261=)
| |
11 | g.22625029G>A | CA380058335 | FANCF | c.782C>T (p.Thr261Ile)
| dbSNP gnomAD v4 |
11 | g.22625029G>C | CA380058336 | FANCF | c.782C>G (p.Thr261Ser)
| dbSNP |
11 | g.22625029G= | CA1957606981 | FANCF | c.782C= (p.Thr261=)
| |
11 | g.22625029G>T | CA380058337 | FANCF | c.782C>A (p.Thr261Asn)
| |
11 | g.22625030T>A | CA380058338 | FANCF | c.781A>T (p.Thr261Ser)
| dbSNP |
11 | g.22625030T>C | CA380058340 | FANCF | c.781A>G (p.Thr261Ala)
| |
11 | g.22625030T>G | CA380058339 | FANCF | c.781A>C (p.Thr261Pro)
| |
11 | g.22625030_22625037delinsTCAAAAGC | CA1957606982 | FANCF | c.774_781delinsGCTTTTGA (p.Gly258=)
| |
11 | g.22625031C>A | CA380058341 | FANCF | c.780G>T (p.Leu260Phe)
| |
11 | g.22625031C>G | CA380058342 | FANCF | c.780G>C (p.Leu260Phe)
| |
11 | g.22625031C>T | CA473533578 | FANCF | c.780G>A (p.Leu260=)
| |
11 | g.22625032_22625038del | CA598390432 | FANCF | c.774_780del (p.Leu260Ter)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625032A>C | CA380058343 | FANCF | c.779T>G (p.Leu260Trp)
| |
11 | g.22625032A>G | CA380058344 | FANCF | c.779T>C (p.Leu260Ser)
| |
11 | g.22625032A>T | CA380058345 | FANCF | c.779T>A (p.Leu260Ter)
| |
11 | g.22625033A= | CA1957606983 | FANCF | c.778T= (p.Leu260=)
| |
11 | g.22625033A>C | CA380058346 | FANCF | c.778T>G (p.Leu260Val)
| dbSNP |
11 | g.22625033A>G | CA473533579 | FANCF | c.778T>C (p.Leu260=)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625033A>T | CA380058347 | FANCF | c.778T>A (p.Leu260Met)
| |
11 | g.22625034A>C | CA473533580 | FANCF | c.777T>G (p.Leu259=)
| |
11 | g.22625034A>G | CA473533581 | FANCF | c.777T>C (p.Leu259=)
| |
11 | g.22625034A>T | CA473533582 | FANCF | c.777T>A (p.Leu259=)
| dbSNP |
11 | g.22625034_22625035insCACACCCAACAC | CA2790714008 | FANCF | c.776_777insGTGTTGGGTGTG (p.Leu259_Leu260insCysTrpValCys)
| |
11 | g.22625035A>C | CA380058348 | FANCF | c.776T>G (p.Leu259Arg)
| |
11 | g.22625035A>G | CA380058349 | FANCF | c.776T>C (p.Leu259Pro)
| |
11 | g.22625035A>T | CA380058350 | FANCF | c.776T>A (p.Leu259His)
| |
11 | g.22625035_22625036insCCAAACACACCCAACACA | CA2790714007 | FANCF | c.776_777insGTGTTGGGTGTGTTTGGT (p.Leu259_Leu260insCysTrpValCysLeuVal)
| |
11 | g.22625036G>A | CA380058351 | FANCF | c.775C>T (p.Leu259Phe)
| |
11 | g.22625036G>C | CA380058352 | FANCF | c.775C>G (p.Leu259Val)
| |
11 | g.22625036G= | CA1957606984 | FANCF | c.775C= (p.Leu259=)
| |
11 | g.22625036G>T | CA380058353 | FANCF | c.775C>A (p.Leu259Ile)
| |
11 | g.22625037C>A | CA473533587 | FANCF | c.774G>T (p.Gly258=)
| |
11 | g.22625037C>G | CA473533588 | FANCF | c.774G>C (p.Gly258=)
| dbSNP |
11 | g.22625037C>T | CA473533589 | FANCF | c.774G>A (p.Gly258=)
| ClinVar dbSNP |
11 | g.22625039dup | CA219086620 | FANCF | c.774dup (p.Leu259AlafsTer7)
| dbSNP |
11 | g.22625038C>A | CA380058354 | FANCF | c.773G>T (p.Gly258Val)
| |
11 | g.22625038C= | CA1957606985 | FANCF | c.773G= (p.Gly258=)
| |
11 | g.22625038C>G | CA219086621 | FANCF | c.773G>C (p.Gly258Ala)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625038C>T | CA380058355 | FANCF | c.773G>A (p.Gly258Glu)
| gnomAD v4 |
11 | g.22625039C>A | CA380058356 | FANCF | c.772G>T (p.Gly258Trp)
| |
11 | g.22625039C= | CA1957606986 | FANCF | c.772G= (p.Gly258=)
| |
11 | g.22625039C>G | CA380058357 | FANCF | c.772G>C (p.Gly258Arg)
| dbSNP |
11 | g.22625039C>T | CA5924263 | FANCF | c.772G>A (p.Gly258Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625040G>A | CA5924264 | FANCF | c.771C>T (p.Ala257=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625040G>C | CA473533594 | FANCF | c.771C>G (p.Ala257=)
| ClinVar gnomAD v4 |
11 | g.22625040G= | CA1957606987 | FANCF | c.771C= (p.Ala257=)
| |
11 | g.22625040G>T | CA473533593 | FANCF | c.771C>A (p.Ala257=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625041G>A | CA380058358 | FANCF | c.770C>T (p.Ala257Val)
| dbSNP |
11 | g.22625041G>C | CA380058359 | FANCF | c.770C>G (p.Ala257Gly)
| |
11 | g.22625041G>T | CA380058360 | FANCF | c.770C>A (p.Ala257Asp)
| |
11 | g.22625042C>A | CA380058361 | FANCF | c.769G>T (p.Ala257Ser)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625042C= | CA1957606988 | FANCF | c.769G= (p.Ala257=)
| |
11 | g.22625042C>G | CA380058362 | FANCF | c.769G>C (p.Ala257Pro)
| dbSNP |
11 | g.22625042C>T | CA380058363 | FANCF | c.769G>A (p.Ala257Thr)
| ClinVar dbSNP |
11 | g.22625043T>A | CA473533601 | FANCF | c.768A>T (p.Pro256=)
| |
11 | g.22625043T>C | CA473533602 | FANCF | c.768A>G (p.Pro256=)
| |
11 | g.22625043T>G | CA473533603 | FANCF | c.768A>C (p.Pro256=)
| |
11 | g.22625044G>A | CA380058365 | FANCF | c.767C>T (p.Pro256Leu)
| dbSNP |
11 | g.22625044G>C | CA380058366 | FANCF | c.767C>G (p.Pro256Arg)
| |
11 | g.22625044G>T | CA380058364 | FANCF | c.767C>A (p.Pro256Gln)
| |
11 | g.22625045G>A | CA219086622 | FANCF | c.766C>T (p.Pro256Ser)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625045G>C | CA380058367 | FANCF | c.766C>G (p.Pro256Ala)
| gnomAD v4 |
11 | g.22625045G= | CA1957606989 | FANCF | c.766C= (p.Pro256=)
| |
11 | g.22625045G>T | CA380058368 | FANCF | c.766C>A (p.Pro256Thr)
| |
11 | g.22625046G>A | CA5924265 | FANCF | c.765C>T (p.Leu255=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625046G>C | CA473533610 | FANCF | c.765C>G (p.Leu255=)
| |
11 | g.22625046G= | CA1957606990 | FANCF | c.765C= (p.Leu255=)
| |
11 | g.22625046G>T | CA473533608 | FANCF | c.765C>A (p.Leu255=)
| gnomAD v4 |
11 | g.22625047A= | CA1957606991 | FANCF | c.764T= (p.Leu255=)
| |
11 | g.22625047A>C | CA380058369 | FANCF | c.764T>G (p.Leu255Arg)
| |
11 | g.22625047A>G | CA380058370 | FANCF | c.764T>C (p.Leu255Pro)
| dbSNP |
11 | g.22625047A>T | CA380058371 | FANCF | c.764T>A (p.Leu255His)
| gnomAD v4 |
11 | g.22625048G>A | CA380058372 | FANCF | c.763C>T (p.Leu255Phe)
| COSMIC |
11 | g.22625048G>C | CA380058373 | FANCF | c.763C>G (p.Leu255Val)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625048G= | CA1957606992 | FANCF | c.763C= (p.Leu255=)
| |
11 | g.22625048G>T | CA380058374 | FANCF | c.763C>A (p.Leu255Ile)
| gnomAD v4 |
11 | g.22625049G>A | CA473533613 | FANCF | c.762C>T (p.Ala254=)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625049G>C | CA473533615 | FANCF | c.762C>G (p.Ala254=)
| |
11 | g.22625049G= | CA1957606993 | FANCF | c.762C= (p.Ala254=)
| |
11 | g.22625049G>T | CA473533617 | FANCF | c.762C>A (p.Ala254=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625052_22625063del | CA2612850462 | FANCF | c.751_762del (p.Phe251_Ala254del)
| gnomAD v4 |
11 | g.22625050G>A | CA380058375 | FANCF | c.761C>T (p.Ala254Val)
| |
11 | g.22625050G>C | CA380058376 | FANCF | c.761C>G (p.Ala254Gly)
| dbSNP |
11 | g.22625050G>T | CA380058377 | FANCF | c.761C>A (p.Ala254Asp)
| |
11 | g.22625051C>A | CA380058379 | FANCF | c.760G>T (p.Ala254Ser)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625051C= | CA1957606994 | FANCF | c.760G= (p.Ala254=)
| |
11 | g.22625051C>G | CA380058380 | FANCF | c.760G>C (p.Ala254Pro)
| |
11 | g.22625051C>T | CA380058378 | FANCF | c.760G>A (p.Ala254Thr)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625052G>A | CA473533621 | FANCF | c.759C>T (p.Arg253=)
| dbSNP gnomAD v4 |
11 | g.22625052G>C | CA473533623 | FANCF | c.759C>G (p.Arg253=)
| |
11 | g.22625052G>T | CA473533622 | FANCF | c.759C>A (p.Arg253=)
| |
11 | g.22625053C>A | CA380058381 | FANCF | c.758G>T (p.Arg253Leu)
| |
11 | g.22625053C>G | CA380058382 | FANCF | c.758G>C (p.Arg253Pro)
| gnomAD v4 |
11 | g.22625053C>T | CA380058383 | FANCF | c.758G>A (p.Arg253His)
| dbSNP |
11 | g.22625054G>A | CA5924266 | FANCF | c.757C>T (p.Arg253Cys)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625054G>C | CA219086623 | FANCF | c.757C>G (p.Arg253Gly)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625054G= | CA1957606995 | FANCF | c.757C= (p.Arg253=)
| |
11 | g.22625054G>T | CA380058384 | FANCF | c.757C>A (p.Arg253Ser)
| |
11 | g.22625055A>C | CA380058385 | FANCF | c.756T>G (p.Cys252Trp)
| |
11 | g.22625055A>G | CA473533627 | FANCF | c.756T>C (p.Cys252=)
| |
11 | g.22625055A>T | CA380058386 | FANCF | c.756T>A (p.Cys252Ter)
| |
11 | g.22625056C>A | CA380058387 | FANCF | c.755G>T (p.Cys252Phe)
| |
11 | g.22625056C= | CA1957606997 | FANCF | c.755G= (p.Cys252=)
| |
11 | g.22625056C>G | CA380058388 | FANCF | c.755G>C (p.Cys252Ser)
| dbSNP |
11 | g.22625056C>T | CA380058389 | FANCF | c.755G>A (p.Cys252Tyr)
| dbSNP |
11 | g.22625056_22625057delinsCA | CA1957606996 | FANCF | c.754_755delinsTG (p.Cys252=)
| |
11 | g.22625057A= | CA1957606998 | FANCF | c.754T= (p.Cys252=)
| |
11 | g.22625057A>C | CA219086624 | FANCF | c.754T>G (p.Cys252Gly)
| dbSNP |
11 | g.22625057A>G | CA380058390 | FANCF | c.754T>C (p.Cys252Arg)
| |
11 | g.22625057A>T | CA380058391 | FANCF | c.754T>A (p.Cys252Ser)
| |
11 | g.22625060del | CA598390433 | FANCF | c.754del (p.Cys252ValfsTer9)
| dbSNP gnomAD v2 gnomAD v4 |
11 | g.22625058A>C | CA380058392 | FANCF | c.753T>G (p.Phe251Leu)
| |
11 | g.22625058A>G | CA473533632 | FANCF | c.753T>C (p.Phe251=)
| gnomAD v4 |
11 | g.22625058A>T | CA380058393 | FANCF | c.753T>A (p.Phe251Leu)
| |
11 | g.22625059A>C | CA380058394 | FANCF | c.752T>G (p.Phe251Cys)
| ClinVar |
11 | g.22625059A>G | CA380058395 | FANCF | c.752T>C (p.Phe251Ser)
| |
11 | g.22625059A>T | CA380058396 | FANCF | c.752T>A (p.Phe251Tyr)
| |
11 | g.22625060A>C | CA380058397 | FANCF | c.751T>G (p.Phe251Val)
| |
11 | g.22625060A>G | CA380058398 | FANCF | c.751T>C (p.Phe251Leu)
| dbSNP |
11 | g.22625060A>T | CA380058399 | FANCF | c.751T>A (p.Phe251Ile)
| |
11 | g.22625061G>A | CA473533637 | FANCF | c.750C>T (p.Ala250=)
| |
11 | g.22625061G>C | CA473533636 | FANCF | c.750C>G (p.Ala250=)
| |
11 | g.22625061G= | CA1957606999 | FANCF | c.750C= (p.Ala250=)
| |
11 | g.22625061G>T | CA219086625 | FANCF | c.750C>A (p.Ala250=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625062G>A | CA219086626 | FANCF | c.749C>T (p.Ala250Val)
| dbSNP gnomAD v4 |
11 | g.22625062G>C | CA380058401 | FANCF | c.749C>G (p.Ala250Gly)
| dbSNP |
11 | g.22625062G= | CA1957607000 | FANCF | c.749C= (p.Ala250=)
| |
11 | g.22625062G>T | CA380058400 | FANCF | c.749C>A (p.Ala250Asp)
| |
11 | g.22625063C>A | CA380058402 | FANCF | c.748G>T (p.Ala250Ser)
| dbSNP |
11 | g.22625063C>G | CA380058403 | FANCF | c.748G>C (p.Ala250Pro)
| |
11 | g.22625063C>T | CA380058404 | FANCF | c.748G>A (p.Ala250Thr)
| gnomAD v4 |
11 | g.22625064A>C | CA473533639 | FANCF | c.747T>G (p.Ala249=)
| |
11 | g.22625064A>G | CA473533640 | FANCF | c.747T>C (p.Ala249=)
| |
11 | g.22625064A>T | CA473533641 | FANCF | c.747T>A (p.Ala249=)
| |
11 | g.22625065G>A | CA380058405 | FANCF | c.746C>T (p.Ala249Val)
| dbSNP gnomAD v4 |
11 | g.22625065G>C | CA380058406 | FANCF | c.746C>G (p.Ala249Gly)
| |
11 | g.22625065G= | CA1957607001 | FANCF | c.746C= (p.Ala249=)
| |
11 | g.22625065G>T | CA380058407 | FANCF | c.746C>A (p.Ala249Asp)
| |
11 | g.22625066C>A | CA380058408 | FANCF | c.745G>T (p.Ala249Ser)
| dbSNP |
11 | g.22625066C>G | CA380058410 | FANCF | c.745G>C (p.Ala249Pro)
| dbSNP |
11 | g.22625066C>T | CA380058409 | FANCF | c.745G>A (p.Ala249Thr)
| dbSNP |
11 | g.22625067A>C | CA380058411 | FANCF | c.744T>G (p.Phe248Leu)
| |
11 | g.22625067A>G | CA473533642 | FANCF | c.744T>C (p.Phe248=)
| gnomAD v4 |
11 | g.22625067A>T | CA380058412 | FANCF | c.744T>A (p.Phe248Leu)
| |