11 | g.22625257_22625259delinsTCC | CA2580082868 | FANCF | c.552_554delinsGGA (p.Pro185Asp)
| ClinVar |
11 | g.22625259A= | CA1957607110 | FANCF | c.552T= (p.Arg184=)
| |
11 | g.22625259A>C | CA473533471 | FANCF | c.552T>G (p.Arg184=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625259A>G | CA473533473 | FANCF | c.552T>C (p.Arg184=)
| dbSNP |
11 | g.22625259A>T | CA473533472 | FANCF | c.552T>A (p.Arg184=)
| dbSNP |
11 | g.22625260C>A | CA380058810 | FANCF | c.551G>T (p.Arg184Leu)
| |
11 | g.22625260C>G | CA380058811 | FANCF | c.551G>C (p.Arg184Pro)
| ClinVar |
11 | g.22625260C>T | CA380058812 | FANCF | c.551G>A (p.Arg184His)
| dbSNP |
11 | g.22625261G>A | CA380058814 | FANCF | c.550C>T (p.Arg184Cys)
| dbSNP |
11 | g.22625261G>C | CA380058815 | FANCF | c.550C>G (p.Arg184Gly)
| |
11 | g.22625261G>T | CA380058813 | FANCF | c.550C>A (p.Arg184Ser)
| |
11 | g.22625262C>A | CA380058817 | FANCF | c.549G>T (p.Glu183Asp)
| |
11 | g.22625262C>G | CA380058816 | FANCF | c.549G>C (p.Glu183Asp)
| |
11 | g.22625262C>T | CA473533477 | FANCF | c.549G>A (p.Glu183=)
| |
11 | g.22625263T>A | CA380058818 | FANCF | c.548A>T (p.Glu183Val)
| dbSNP |
11 | g.22625263T>C | CA380058819 | FANCF | c.548A>G (p.Glu183Gly)
| dbSNP |
11 | g.22625263T>G | CA380058820 | FANCF | c.548A>C (p.Glu183Ala)
| |
11 | g.22625264C>A | CA380058821 | FANCF | c.547G>T (p.Glu183Ter)
| |
11 | g.22625264C= | CA1957607111 | FANCF | c.547G= (p.Glu183=)
| |
11 | g.22625264C>G | CA10630686 | FANCF | c.547G>C (p.Glu183Gln)
| ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.22625264C>T | CA5924312 | FANCF | c.547G>A (p.Glu183Lys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625265C>A | CA473533481 | FANCF | c.546G>T (p.Ala182=)
| |
11 | g.22625265C= | CA1957607112 | FANCF | c.546G= (p.Ala182=)
| |
11 | g.22625265C>G | CA473533483 | FANCF | c.546G>C (p.Ala182=)
| |
11 | g.22625265C>T | CA473533482 | FANCF | c.546G>A (p.Ala182=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625266G>A | CA380058822 | FANCF | c.545C>T (p.Ala182Val)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625266G>C | CA380058823 | FANCF | c.545C>G (p.Ala182Gly)
| dbSNP |
11 | g.22625266G= | CA1957607113 | FANCF | c.545C= (p.Ala182=)
| |
11 | g.22625266G>T | CA380058824 | FANCF | c.545C>A (p.Ala182Glu)
| dbSNP |
11 | g.22625267C>A | CA380058825 | FANCF | c.544G>T (p.Ala182Ser)
| |
11 | g.22625267C= | CA1957607114 | FANCF | c.544G= (p.Ala182=)
| |
11 | g.22625267C>G | CA380058826 | FANCF | c.544G>C (p.Ala182Pro)
| |
11 | g.22625267C>T | CA380058827 | FANCF | c.544G>A (p.Ala182Thr)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625268T>A | CA380058828 | FANCF | c.543A>T (p.Glu181Asp)
| |
11 | g.22625268T>C | CA473533487 | FANCF | c.543A>G (p.Glu181=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625268T>G | CA380058829 | FANCF | c.543A>C (p.Glu181Asp)
| |
11 | g.22625268T= | CA1957607115 | FANCF | c.543A= (p.Glu181=)
| |
11 | g.22625269T>A | CA380058830 | FANCF | c.542A>T (p.Glu181Val)
| |
11 | g.22625269T>C | CA380058831 | FANCF | c.542A>G (p.Glu181Gly)
| |
11 | g.22625269T>G | CA380058832 | FANCF | c.542A>C (p.Glu181Ala)
| |
11 | g.22625270C>A | CA380058833 | FANCF | c.541G>T (p.Glu181Ter)
| |
11 | g.22625270C>G | CA380058834 | FANCF | c.541G>C (p.Glu181Gln)
| |
11 | g.22625270C>T | CA380058835 | FANCF | c.541G>A (p.Glu181Lys)
| dbSNP |
11 | g.22625271G>A | CA473533489 | FANCF | c.540C>T (p.Ala180=)
| gnomAD v4 |
11 | g.22625271G>C | CA473533490 | FANCF | c.540C>G (p.Ala180=)
| dbSNP |
11 | g.22625271G= | CA1957607116 | FANCF | c.540C= (p.Ala180=)
| |
11 | g.22625271G>T | CA473533491 | FANCF | c.540C>A (p.Ala180=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625272G>A | CA5924313 | FANCF | c.539C>T (p.Ala180Val)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625272G>C | CA380058836 | FANCF | c.539C>G (p.Ala180Gly)
| dbSNP |
11 | g.22625272G= | CA1957607117 | FANCF | c.539C= (p.Ala180=)
| |
11 | g.22625272G>T | CA380058837 | FANCF | c.539C>A (p.Ala180Asp)
| |
11 | g.22625273C>A | CA380058838 | FANCF | c.538G>T (p.Ala180Ser)
| |
11 | g.22625273C>G | CA380058839 | FANCF | c.538G>C (p.Ala180Pro)
| |
11 | g.22625273C>T | CA380058840 | FANCF | c.538G>A (p.Ala180Thr)
| dbSNP |
11 | g.22625274del | CA2580082869 | FANCF | c.538del (p.Ala180ProfsTer23)
| ClinVar |
11 | g.22625273_22625281delinsCCTTCCCCA | CA1957607118 | FANCF | c.530_538delinsTGGGGAAGG (p.Val177=)
| |
11 | g.22625274C>A | CA380058841 | FANCF | c.537G>T (p.Lys179Asn)
| |
11 | g.22625274C= | CA1957607120 | FANCF | c.537G= (p.Lys179=)
| |
11 | g.22625274C>G | CA380058842 | FANCF | c.537G>C (p.Lys179Asn)
| ClinVar dbSNP |
11 | g.22625274C>T | CA5924314 | FANCF | c.537G>A (p.Lys179=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625275_22625282del | CA1957607119 | FANCF | c.530_537del (p.Val177GlyfsTer?)
| ClinVar dbSNP |
11 | g.22625275T>A | CA380058843 | FANCF | c.536A>T (p.Lys179Met)
| dbSNP |
11 | g.22625275T>C | CA380058844 | FANCF | c.536A>G (p.Lys179Arg)
| dbSNP |
11 | g.22625275T>G | CA380058845 | FANCF | c.536A>C (p.Lys179Thr)
| |
11 | g.22625276T>A | CA380058846 | FANCF | c.535A>T (p.Lys179Ter)
| ClinVar |
11 | g.22625276T>C | CA380058847 | FANCF | c.535A>G (p.Lys179Glu)
| dbSNP |
11 | g.22625276T>G | CA380058848 | FANCF | c.535A>C (p.Lys179Gln)
| |
11 | g.22625277C>A | CA473533492 | FANCF | c.534G>T (p.Gly178=)
| |
11 | g.22625277C>G | CA473533493 | FANCF | c.534G>C (p.Gly178=)
| gnomAD v4 |
11 | g.22625277C>T | CA473533494 | FANCF | c.534G>A (p.Gly178=)
| |
11 | g.22625280del | CA2499220871 | FANCF | c.534del (p.Lys179ArgfsTer24)
| ClinVar dbSNP |
11 | g.22625278C>A | CA380058851 | FANCF | c.533G>T (p.Gly178Val)
| |
11 | g.22625278C>G | CA380058849 | FANCF | c.533G>C (p.Gly178Ala)
| |
11 | g.22625278C>T | CA380058850 | FANCF | c.533G>A (p.Gly178Glu)
| ClinVar dbSNP |
11 | g.22625279C>A | CA380058852 | FANCF | c.532G>T (p.Gly178Trp)
| |
11 | g.22625279C= | CA1957607121 | FANCF | c.532G= (p.Gly178=)
| |
11 | g.22625279C>G | CA380058853 | FANCF | c.532G>C (p.Gly178Arg)
| dbSNP gnomAD v4 |
11 | g.22625279C>T | CA380058854 | FANCF | c.532G>A (p.Gly178Arg)
| |
11 | g.22625280C>A | CA473533495 | FANCF | c.531G>T (p.Val177=)
| dbSNP |
11 | g.22625280C>G | CA473533496 | FANCF | c.531G>C (p.Val177=)
| |
11 | g.22625280C>T | CA473533497 | FANCF | c.531G>A (p.Val177=)
| |
11 | g.22625281A= | CA1957607122 | FANCF | c.530T= (p.Val177=)
| |
11 | g.22625281A>C | CA380058855 | FANCF | c.530T>G (p.Val177Gly)
| dbSNP |
11 | g.22625281A>G | CA380058856 | FANCF | c.530T>C (p.Val177Ala)
| |
11 | g.22625281A>T | CA380058857 | FANCF | c.530T>A (p.Val177Glu)
| |
11 | g.22625282C>A | CA380058858 | FANCF | c.529G>T (p.Val177Leu)
| |
11 | g.22625282C= | CA1957607123 | FANCF | c.529G= (p.Val177=)
| |
11 | g.22625282C>G | CA380058859 | FANCF | c.529G>C (p.Val177Leu)
| |
11 | g.22625282C>T | CA5924315 | FANCF | c.529G>A (p.Val177Met)
| ClinVar dbSNP ExAC gnomAD v2 |
11 | g.22625283del | CA2612850467 | FANCF | c.529del (p.Val177TrpfsTer26)
| gnomAD v4 |
11 | g.22625283C>A | CA380058860 | FANCF | c.528G>T (p.Glu176Asp)
| dbSNP |
11 | g.22625283C= | CA1957607124 | FANCF | c.528G= (p.Glu176=)
| |
11 | g.22625283C>G | CA380058861 | FANCF | c.528G>C (p.Glu176Asp)
| |
11 | g.22625283C>T | CA473533498 | FANCF | c.528G>A (p.Glu176=)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.22625284T>A | CA380058862 | FANCF | c.527A>T (p.Glu176Val)
| |
11 | g.22625284T>C | CA380058863 | FANCF | c.527A>G (p.Glu176Gly)
| COSMIC |
11 | g.22625284T>G | CA380058864 | FANCF | c.527A>C (p.Glu176Ala)
| |
11 | g.22625285C>A | CA380058865 | FANCF | c.526G>T (p.Glu176Ter)
| |
11 | g.22625285C>G | CA380058866 | FANCF | c.526G>C (p.Glu176Gln)
| |
11 | g.22625285C>T | CA380058867 | FANCF | c.526G>A (p.Glu176Lys)
| |
11 | g.22625286C>A | CA380058868 | FANCF | c.525G>T (p.Gln175His)
| |
11 | g.22625286C>G | CA380058869 | FANCF | c.525G>C (p.Gln175His)
| |
11 | g.22625286C>T | CA473533499 | FANCF | c.525G>A (p.Gln175=)
| |
11 | g.22625287T>A | CA219086638 | FANCF | c.524A>T (p.Gln175Leu)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625287T>C | CA380058870 | FANCF | c.524A>G (p.Gln175Arg)
| |
11 | g.22625287T>G | CA380058871 | FANCF | c.524A>C (p.Gln175Pro)
| |
11 | g.22625287T= | CA1957607125 | FANCF | c.524A= (p.Gln175=)
| |
11 | g.22625288G>A | CA380058873 | FANCF | c.523C>T (p.Gln175Ter)
| dbSNP |
11 | g.22625288G>C | CA380058874 | FANCF | c.523C>G (p.Gln175Glu)
| dbSNP |
11 | g.22625288G>T | CA380058872 | FANCF | c.523C>A (p.Gln175Lys)
| |
11 | g.22625289C>A | CA473533500 | FANCF | c.522G>T (p.Leu174=)
| dbSNP |
11 | g.22625289C>G | CA473533501 | FANCF | c.522G>C (p.Leu174=)
| |
11 | g.22625289C>T | CA473533502 | FANCF | c.522G>A (p.Leu174=)
| dbSNP |
11 | g.22625290A>C | CA380058875 | FANCF | c.521T>G (p.Leu174Arg)
| |
11 | g.22625290A>G | CA380058877 | FANCF | c.521T>C (p.Leu174Pro)
| dbSNP |
11 | g.22625290A>T | CA380058876 | FANCF | c.521T>A (p.Leu174Gln)
| |
11 | g.22625291G>A | CA5924316 | FANCF | c.520C>T (p.Leu174=)
| dbSNP ExAC |
11 | g.22625291G>C | CA380058879 | FANCF | c.520C>G (p.Leu174Val)
| dbSNP |
11 | g.22625291G= | CA1957607126 | FANCF | c.520C= (p.Leu174=)
| |
11 | g.22625291G>T | CA380058878 | FANCF | c.520C>A (p.Leu174Met)
| |
11 | g.22625292A= | CA1957607127 | FANCF | c.519T= (p.Arg173=)
| |
11 | g.22625292A>C | CA473533503 | FANCF | c.519T>G (p.Arg173=)
| |
11 | g.22625292A>G | CA219086639 | FANCF | c.519T>C (p.Arg173=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625292A>T | CA473533504 | FANCF | c.519T>A (p.Arg173=)
| dbSNP |
11 | g.22625293C>A | CA380058880 | FANCF | c.518G>T (p.Arg173Leu)
| |
11 | g.22625293C= | CA1957607128 | FANCF | c.518G= (p.Arg173=)
| |
11 | g.22625293C>G | CA5924317 | FANCF | c.518G>C (p.Arg173Pro)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625293C>T | CA380058881 | FANCF | c.518G>A (p.Arg173His)
| dbSNP |
11 | g.22625294G>A | CA380058882 | FANCF | c.517C>T (p.Arg173Cys)
| dbSNP |
11 | g.22625294G>C | CA380058883 | FANCF | c.517C>G (p.Arg173Gly)
| dbSNP |
11 | g.22625294G>T | CA380058884 | FANCF | c.517C>A (p.Arg173Ser)
| |
11 | g.22625295C>A | CA380058885 | FANCF | c.516G>T (p.Glu172Asp)
| |
11 | g.22625295C>G | CA380058886 | FANCF | c.516G>C (p.Glu172Asp)
| |
11 | g.22625295C>T | CA473533505 | FANCF | c.516G>A (p.Glu172=)
| |
11 | g.22625296T>A | CA380058887 | FANCF | c.515A>T (p.Glu172Val)
| |
11 | g.22625296T>C | CA380058888 | FANCF | c.515A>G (p.Glu172Gly)
| dbSNP gnomAD v4 |
11 | g.22625296T>G | CA380058889 | FANCF | c.515A>C (p.Glu172Ala)
| |
11 | g.22625297C>A | CA380058890 | FANCF | c.514G>T (p.Glu172Ter)
| |
11 | g.22625297C= | CA1957607129 | FANCF | c.514G= (p.Glu172=)
| |
11 | g.22625297C>G | CA380058891 | FANCF | c.514G>C (p.Glu172Gln)
| gnomAD v4 |
11 | g.22625297C>T | CA380058892 | FANCF | c.514G>A (p.Glu172Lys)
| dbSNP gnomAD v2 |
11 | g.22625298C>A | CA473533506 | FANCF | c.513G>T (p.Leu171=)
| gnomAD v4 |
11 | g.22625298C= | CA1957607130 | FANCF | c.513G= (p.Leu171=)
| |
11 | g.22625298C>G | CA473533507 | FANCF | c.513G>C (p.Leu171=)
| |
11 | g.22625298C>T | CA473533508 | FANCF | c.513G>A (p.Leu171=)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.22625299A= | CA1957607131 | FANCF | c.512T= (p.Leu171=)
| |
11 | g.22625299A>C | CA380058895 | FANCF | c.512T>G (p.Leu171Arg)
| |
11 | g.22625299A>G | CA380058893 | FANCF | c.512T>C (p.Leu171Pro)
| dbSNP |
11 | g.22625299A>T | CA380058894 | FANCF | c.512T>A (p.Leu171Gln)
| |
11 | g.22625300G>A | CA473533509 | FANCF | c.511C>T (p.Leu171=)
| dbSNP |
11 | g.22625300G>C | CA380058896 | FANCF | c.511C>G (p.Leu171Val)
| |
11 | g.22625300G>T | CA380058897 | FANCF | c.511C>A (p.Leu171Met)
| |
11 | g.22625301C>A | CA473533510 | FANCF | c.510G>T (p.Leu170=)
| |
11 | g.22625301C>G | CA473533512 | FANCF | c.510G>C (p.Leu170=)
| |
11 | g.22625301C>T | CA473533511 | FANCF | c.510G>A (p.Leu170=)
| dbSNP |
11 | g.22625302A>C | CA380058898 | FANCF | c.509T>G (p.Leu170Arg)
| |
11 | g.22625302A>G | CA380058899 | FANCF | c.509T>C (p.Leu170Pro)
| |
11 | g.22625302A>T | CA380058900 | FANCF | c.509T>A (p.Leu170Gln)
| gnomAD v4 |
11 | g.22625303G>A | CA473533513 | FANCF | c.508C>T (p.Leu170=)
| dbSNP |
11 | g.22625303G>C | CA380058901 | FANCF | c.508C>G (p.Leu170Val)
| |
11 | g.22625303G>T | CA380058902 | FANCF | c.508C>A (p.Leu170Met)
| |
11 | g.22625304C>A | CA473533514 | FANCF | c.507G>T (p.Leu169=)
| |
11 | g.22625304C= | CA1957607132 | FANCF | c.507G= (p.Leu169=)
| |
11 | g.22625304C>G | CA473533515 | FANCF | c.507G>C (p.Leu169=)
| |
11 | g.22625304C>T | CA473533516 | FANCF | c.507G>A (p.Leu169=)
| ClinVar dbSNP gnomAD v4 |
11 | g.22625305A= | CA1957607133 | FANCF | c.506T= (p.Leu169=)
| |
11 | g.22625305A>C | CA380058903 | FANCF | c.506T>G (p.Leu169Arg)
| |
11 | g.22625305A>G | CA380058904 | FANCF | c.506T>C (p.Leu169Pro)
| |
11 | g.22625305A>T | CA219086640 | FANCF | c.506T>A (p.Leu169Gln)
| ClinVar dbSNP |
11 | g.22625306G>A | CA473533517 | FANCF | c.505C>T (p.Leu169=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625306G>C | CA380058906 | FANCF | c.505C>G (p.Leu169Val)
| |
11 | g.22625306G= | CA1957607134 | FANCF | c.505C= (p.Leu169=)
| |
11 | g.22625306G>T | CA380058905 | FANCF | c.505C>A (p.Leu169Met)
| gnomAD v4 |
11 | g.22625306_22625307delinsAT | CA2739270376 | FANCF | c.504_505delinsAT (p.Glu168=)
| ClinVar |
11 | g.22625307C>A | CA380058907 | FANCF | c.504G>T (p.Glu168Asp)
| |
11 | g.22625307C= | CA1957607135 | FANCF | c.504G= (p.Glu168=)
| |
11 | g.22625307C>G | CA380058908 | FANCF | c.504G>C (p.Glu168Asp)
| |
11 | g.22625307C>T | CA473533518 | FANCF | c.504G>A (p.Glu168=)
| dbSNP gnomAD v3 gnomAD v4 |
11 | g.22625308T>A | CA380058909 | FANCF | c.503A>T (p.Glu168Val)
| |
11 | g.22625308T>C | CA380058910 | FANCF | c.503A>G (p.Glu168Gly)
| gnomAD v4 |
11 | g.22625308T>G | CA380058911 | FANCF | c.503A>C (p.Glu168Ala)
| |
11 | g.22625309C>A | CA5924318 | FANCF | c.502G>T (p.Glu168Ter)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.22625309C= | CA1957607136 | FANCF | c.502G= (p.Glu168=)
| |
11 | g.22625309C>G | CA380058912 | FANCF | c.502G>C (p.Glu168Gln)
| |
11 | g.22625309C>T | CA380058913 | FANCF | c.502G>A (p.Glu168Lys)
| |
11 | g.22625310C>A | CA473533519 | FANCF | c.501G>T (p.Ala167=)
| |
11 | g.22625310C>G | CA473533520 | FANCF | c.501G>C (p.Ala167=)
| |
11 | g.22625310C>T | CA473533521 | FANCF | c.501G>A (p.Ala167=)
| ClinVar gnomAD v4 |
11 | g.22625311G>A | CA5924319 | FANCF | c.500C>T (p.Ala167Val)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.22625311G>C | CA380058914 | FANCF | c.500C>G (p.Ala167Gly)
| dbSNP |
11 | g.22625311G= | CA1957607137 | FANCF | c.500C= (p.Ala167=)
| |
11 | g.22625311G>T | CA380058915 | FANCF | c.500C>A (p.Ala167Glu)
| |
11 | g.22625312C>A | CA380058916 | FANCF | c.499G>T (p.Ala167Ser)
| |
11 | g.22625312C>G | CA380058917 | FANCF | c.499G>C (p.Ala167Pro)
| |
11 | g.22625312C>T | CA380058918 | FANCF | c.499G>A (p.Ala167Thr)
| |
11 | g.22625313C>A | CA380058919 | FANCF | c.498G>T (p.Gln166His)
| |
11 | g.22625313C>G | CA380058920 | FANCF | c.498G>C (p.Gln166His)
| |
11 | g.22625313C>T | CA473533522 | FANCF | c.498G>A (p.Gln166=)
| gnomAD v4 |
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=)
| |