Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.172665641_172665725delinsCATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAA | CA1207431644 | FASLG | c.471_555delinsCATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAA (p.Ser157=) c.*41_*125delinsCATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAA (n.*41_*125delinsCATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAA) | |
1 | g.172665642_172665726delinsATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAAA | CA1141189174 | FASLG | c.472_556delinsATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAAA (p.Met158=) c.*42_*126delinsATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAAA (n.*42_*126delinsATGCCTCTGGAATGGGAAGACACCTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGGCCTTGTGATCAATGAAA) | |
1 | g.172665643_172665726del | CA126563 | FASLG | c.473_556del (p.Met158_Glu185del) c.*43_*126del (n.*43_*126del) | ClinVar dbSNP |
1 | g.172665653A>C | CA343805950 | FASLG | c.483A>C (p.Glu161Asp) c.*53A>C (n.*53A>C) | |
1 | g.172665653A>G | CA421944415 | FASLG | c.483A>G (p.Glu161=) c.*53A>G (n.*53A>G) | gnomAD v4 |
1 | g.172665653A>T | CA343805951 | FASLG | c.483A>T (p.Glu161Asp) c.*53A>T (n.*53A>T) | |
1 | g.172665654T>A | CA343805952 | FASLG | c.484T>A (p.Trp162Arg) c.*54T>A (n.*54T>A) | |
1 | g.172665654T>C | CA343805953 | FASLG | c.484T>C (p.Trp162Arg) c.*54T>C (n.*54T>C) | ClinVar dbSNP |
1 | g.172665654T>G | CA343805954 | FASLG | c.484T>G (p.Trp162Gly) c.*54T>G (n.*54T>G) | |
1 | g.172665655G>A | CA343805957 | FASLG | c.485G>A (p.Trp162Ter) c.*55G>A (n.*55G>A) | |
1 | g.172665655G>C | CA343805956 | FASLG | c.485G>C (p.Trp162Ser) c.*55G>C (n.*55G>C) | |
1 | g.172665655G>T | CA343805955 | FASLG | c.485G>T (p.Trp162Leu) c.*55G>T (n.*55G>T) | |
1 | g.172665656G>A | CA343805958 | FASLG | c.486G>A (p.Trp162Ter) c.*56G>A (n.*56G>A) | |
1 | g.172665656G>C | CA343805960 | FASLG | c.486G>C (p.Trp162Cys) c.*56G>C (n.*56G>C) | |
1 | g.172665656G>T | CA343805959 | FASLG | c.486G>T (p.Trp162Cys) c.*56G>T (n.*56G>T) | gnomAD v4 |
1 | g.172665657G>A | CA343805961 | FASLG | c.487G>A (p.Glu163Lys) c.*57G>A (n.*57G>A) | COSMIC |
1 | g.172665657G>C | CA343805962 | FASLG | c.487G>C (p.Glu163Gln) c.*57G>C (n.*57G>C) | |
1 | g.172665657G>T | CA343805963 | FASLG | c.487G>T (p.Glu163Ter) c.*57G>T (n.*57G>T) | |
1 | g.172665658A>C | CA343805964 | FASLG | c.488A>C (p.Glu163Ala) c.*58A>C (n.*58A>C) | |
1 | g.172665658A>G | CA343805965 | FASLG | c.488A>G (p.Glu163Gly) c.*58A>G (n.*58A>G) | |
1 | g.172665658A>T | CA343805966 | FASLG | c.488A>T (p.Glu163Val) c.*58A>T (n.*58A>T) | |
1 | g.172665659A>C | CA343805967 | FASLG | c.489A>C (p.Glu163Asp) c.*59A>C (n.*59A>C) | |
1 | g.172665659A>G | CA421944416 | FASLG | c.489A>G (p.Glu163=) c.*59A>G (n.*59A>G) | |
1 | g.172665659A>T | CA343805968 | FASLG | c.489A>T (p.Glu163Asp) c.*59A>T (n.*59A>T) | |
1 | g.172665660G>A | CA343805969 | FASLG | c.490G>A (p.Asp164Asn) c.*60G>A (n.*60G>A) | |
1 | g.172665660G>C | CA343805970 | FASLG | c.490G>C (p.Asp164His) c.*60G>C (n.*60G>C) | |
1 | g.172665660G>T | CA343805971 | FASLG | c.490G>T (p.Asp164Tyr) c.*60G>T (n.*60G>T) | |
1 | g.172665661A= | CA1207431648 | FASLG | c.491A= (p.Asp164=) c.*61A= (n.*61A=) | |
1 | g.172665661A>C | CA343805974 | FASLG | c.491A>C (p.Asp164Ala) c.*61A>C (n.*61A>C) | |
1 | g.172665661A>G | CA343805972 | FASLG | c.491A>G (p.Asp164Gly) c.*61A>G (n.*61A>G) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665661A>T | CA343805973 | FASLG | c.491A>T (p.Asp164Val) c.*61A>T (n.*61A>T) | |
1 | g.172665662C>A | CA343805975 | FASLG | c.492C>A (p.Asp164Glu) c.*62C>A (n.*62C>A) | gnomAD v4 |
1 | g.172665662C= | CA1207431649 | FASLG | c.492C= (p.Asp164=) c.*62C= (n.*62C=) | |
1 | g.172665662C>G | CA343805976 | FASLG | c.492C>G (p.Asp164Glu) c.*62C>G (n.*62C>G) | |
1 | g.172665662C>T | CA421944417 | FASLG | c.492C>T (p.Asp164=) c.*62C>T (n.*62C>T) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.172665663A= | CA1149075042 | FASLG | c.493A= (p.Thr165=) c.*63A= (n.*63A=) | |
1 | g.172665663A>C | CA343805977 | FASLG | c.493A>C (p.Thr165Pro) c.*63A>C (n.*63A>C) | |
1 | g.172665663A>G | CA1247581 | FASLG | c.493A>G (p.Thr165Ala) c.*63A>G (n.*63A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.172665663A>T | CA343805978 | FASLG | c.493A>T (p.Thr165Ser) c.*63A>T (n.*63A>T) | |
1 | g.172665664C>A | CA343805979 | FASLG | c.494C>A (p.Thr165Asn) c.*64C>A (n.*64C>A) | dbSNP |
1 | g.172665664C= | CA1207431650 | FASLG | c.494C= (p.Thr165=) c.*64C= (n.*64C=) | |
1 | g.172665664C>G | CA343805980 | FASLG | c.494C>G (p.Thr165Ser) c.*64C>G (n.*64C>G) | |
1 | g.172665664C>T | CA343805981 | FASLG | c.494C>T (p.Thr165Ile) c.*64C>T (n.*64C>T) | ClinVar dbSNP gnomAD v2 |
1 | g.172665665C>A | CA421944418 | FASLG | c.495C>A (p.Thr165=) c.*65C>A (n.*65C>A) | gnomAD v4 COSMIC |
1 | g.172665665C= | CA1207431651 | FASLG | c.495C= (p.Thr165=) c.*65C= (n.*65C=) | |
1 | g.172665665C>G | CA421944419 | FASLG | c.495C>G (p.Thr165=) c.*65C>G (n.*65C>G) | |
1 | g.172665665C>T | CA421944420 | FASLG | c.495C>T (p.Thr165=) c.*65C>T (n.*65C>T) | dbSNP gnomAD v2 |
1 | g.172665666T>A | CA343805982 | FASLG | c.496T>A (p.Tyr166Asn) c.*66T>A (n.*66T>A) | |
1 | g.172665666T>C | CA343805983 | FASLG | c.496T>C (p.Tyr166His) c.*66T>C (n.*66T>C) | |
1 | g.172665666T>G | CA343805984 | FASLG | c.496T>G (p.Tyr166Asp) c.*66T>G (n.*66T>G) | |
1 | g.172665667A= | CA1207431652 | FASLG | c.497A= (p.Tyr166=) c.*67A= (n.*67A=) | |
1 | g.172665667A>C | CA343805986 | FASLG | c.497A>C (p.Tyr166Ser) c.*67A>C (n.*67A>C) | |
1 | g.172665667A>G | CA1247582 | FASLG | c.497A>G (p.Tyr166Cys) c.*67A>G (n.*67A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665667A>T | CA343805985 | FASLG | c.497A>T (p.Tyr166Phe) c.*67A>T (n.*67A>T) | |
1 | g.172665668T>A | CA343805988 | FASLG | c.498T>A (p.Tyr166Ter) c.*68T>A (n.*68T>A) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665668T>C | CA421944421 | FASLG | c.498T>C (p.Tyr166=) c.*68T>C (n.*68T>C) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.172665668T>G | CA343805987 | FASLG | c.498T>G (p.Tyr166Ter) c.*68T>G (n.*68T>G) | |
1 | g.172665668T= | CA1207431653 | FASLG | c.498T= (p.Tyr166=) c.*68T= (n.*68T=) | |
1 | g.172665669G>A | CA343805989 | FASLG | c.499G>A (p.Gly167Arg) c.*69G>A (n.*69G>A) | COSMIC |
1 | g.172665669G>C | CA343805990 | FASLG | c.499G>C (p.Gly167Arg) c.*69G>C (n.*69G>C) | |
1 | g.172665669G>T | CA343805991 | FASLG | c.499G>T (p.Gly167Ter) c.*69G>T (n.*69G>T) | |
1 | g.172665670G>A | CA343805992 | FASLG | c.500G>A (p.Gly167Glu) c.*70G>A (n.*70G>A) | |
1 | g.172665670G>C | CA343805993 | FASLG | c.500G>C (p.Gly167Ala) c.*70G>C (n.*70G>C) | |
1 | g.172665670G>T | CA343805994 | FASLG | c.500G>T (p.Gly167Val) c.*70G>T (n.*70G>T) | |
1 | g.172665671A>C | CA421944422 | FASLG | c.501A>C (p.Gly167=) c.*71A>C (n.*71A>C) | |
1 | g.172665671A>G | CA421944423 | FASLG | c.501A>G (p.Gly167=) c.*71A>G (n.*71A>G) | |
1 | g.172665671A>T | CA421944424 | FASLG | c.501A>T (p.Gly167=) c.*71A>T (n.*71A>T) | |
1 | g.172665672A>C | CA343805995 | FASLG | c.502A>C (p.Ile168Leu) c.*72A>C (n.*72A>C) | |
1 | g.172665672A>G | CA343805997 | FASLG | c.502A>G (p.Ile168Val) c.*72A>G (n.*72A>G) | |
1 | g.172665672A>T | CA343805996 | FASLG | c.502A>T (p.Ile168Phe) c.*72A>T (n.*72A>T) | |
1 | g.172665673T>A | CA343805998 | FASLG | c.503T>A (p.Ile168Asn) c.*73T>A (n.*73T>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.172665673T>C | CA343805999 | FASLG | c.503T>C (p.Ile168Thr) c.*73T>C (n.*73T>C) | |
1 | g.172665673T>G | CA343806000 | FASLG | c.503T>G (p.Ile168Ser) c.*73T>G (n.*73T>G) | |
1 | g.172665673T= | CA1207431654 | FASLG | c.503T= (p.Ile168=) c.*73T= (n.*73T=) | |
1 | g.172665674T>A | CA421944425 | FASLG | c.504T>A (p.Ile168=) c.*74T>A (n.*74T>A) | gnomAD v4 |
1 | g.172665674T>C | CA421944426 | FASLG | c.504T>C (p.Ile168=) c.*74T>C (n.*74T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665674T>G | CA343806001 | FASLG | c.504T>G (p.Ile168Met) c.*74T>G (n.*74T>G) | |
1 | g.172665674T= | CA1207431655 | FASLG | c.504T= (p.Ile168=) c.*74T= (n.*74T=) | |
1 | g.172665675G>A | CA343806002 | FASLG | c.505G>A (p.Val169Ile) c.*75G>A (n.*75G>A) | |
1 | g.172665675G>C | CA343806004 | FASLG | c.505G>C (p.Val169Leu) c.*75G>C (n.*75G>C) | |
1 | g.172665675G>T | CA343806003 | FASLG | c.505G>T (p.Val169Phe) c.*75G>T (n.*75G>T) | |
1 | g.172665676T>A | CA343806005 | FASLG | c.506T>A (p.Val169Asp) c.*76T>A (n.*76T>A) | |
1 | g.172665676T>C | CA343806006 | FASLG | c.506T>C (p.Val169Ala) c.*76T>C (n.*76T>C) | dbSNP |
1 | g.172665676T>G | CA343806007 | FASLG | c.506T>G (p.Val169Gly) c.*76T>G (n.*76T>G) | |
1 | g.172665676T= | CA1207431656 | FASLG | c.506T= (p.Val169=) c.*76T= (n.*76T=) | |
1 | g.172665677C>A | CA421944427 | FASLG | c.507C>A (p.Val169=) c.*77C>A (n.*77C>A) | |
1 | g.172665677C>G | CA421944429 | FASLG | c.507C>G (p.Val169=) c.*77C>G (n.*77C>G) | |
1 | g.172665677C>T | CA421944428 | FASLG | c.507C>T (p.Val169=) c.*77C>T (n.*77C>T) | |
1 | g.172665678C>A | CA343806008 | FASLG | c.508C>A (p.Leu170Met) c.*78C>A (n.*78C>A) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665678C= | CA1207431657 | FASLG | c.508C= (p.Leu170=) c.*78C= (n.*78C=) | |
1 | g.172665678C>G | CA343806009 | FASLG | c.508C>G (p.Leu170Val) c.*78C>G (n.*78C>G) | gnomAD v4 |
1 | g.172665678C>T | CA421944430 | FASLG | c.508C>T (p.Leu170=) c.*78C>T (n.*78C>T) | |
1 | g.172665679T>A | CA343806010 | FASLG | c.509T>A (p.Leu170Gln) c.*79T>A (n.*79T>A) | |
1 | g.172665679T>C | CA343806011 | FASLG | c.509T>C (p.Leu170Pro) c.*79T>C (n.*79T>C) | |
1 | g.172665679T>G | CA343806012 | FASLG | c.509T>G (p.Leu170Arg) c.*79T>G (n.*79T>G) | |
1 | g.172665680G>A | CA421944431 | FASLG | c.510G>A (p.Leu170=) c.*80G>A (n.*80G>A) | |
1 | g.172665680G>C | CA421944432 | FASLG | c.510G>C (p.Leu170=) c.*80G>C (n.*80G>C) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665680G= | CA1207431658 | FASLG | c.510G= (p.Leu170=) c.*80G= (n.*80G=) | |
1 | g.172665680G>T | CA421944433 | FASLG | c.510G>T (p.Leu170=) c.*80G>T (n.*80G>T) | |
1 | g.172665681C>A | CA343806013 | FASLG | c.511C>A (p.Leu171Ile) c.*81C>A (n.*81C>A) | |
1 | g.172665681C>G | CA343806014 | FASLG | c.511C>G (p.Leu171Val) c.*81C>G (n.*81C>G) | |
1 | g.172665681C>T | CA343806015 | FASLG | c.511C>T (p.Leu171Phe) c.*81C>T (n.*81C>T) | |
1 | g.172665682T>A | CA343806018 | FASLG | c.512T>A (p.Leu171His) c.*82T>A (n.*82T>A) | gnomAD v4 |
1 | g.172665682T>C | CA343806017 | FASLG | c.512T>C (p.Leu171Pro) c.*82T>C (n.*82T>C) | COSMIC |
1 | g.172665682T>G | CA343806016 | FASLG | c.512T>G (p.Leu171Arg) c.*82T>G (n.*82T>G) | |
1 | g.172665683T>A | CA421944434 | FASLG | c.513T>A (p.Leu171=) c.*83T>A (n.*83T>A) | |
1 | g.172665683T>C | CA421944435 | FASLG | c.513T>C (p.Leu171=) c.*83T>C (n.*83T>C) | |
1 | g.172665683T>G | CA421944436 | FASLG | c.513T>G (p.Leu171=) c.*83T>G (n.*83T>G) | |
1 | g.172665684T>A | CA343806019 | FASLG | c.514T>A (p.Ser172Thr) c.*84T>A (n.*84T>A) | |
1 | g.172665684T>C | CA343806021 | FASLG | c.514T>C (p.Ser172Pro) c.*84T>C (n.*84T>C) | |
1 | g.172665684T>G | CA343806020 | FASLG | c.514T>G (p.Ser172Ala) c.*84T>G (n.*84T>G) | |
1 | g.172665685C>A | CA1247583 | FASLG | c.515C>A (p.Ser172Tyr) c.*85C>A (n.*85C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.172665685C= | CA1207431659 | FASLG | c.515C= (p.Ser172=) c.*85C= (n.*85C=) | |
1 | g.172665685C>G | CA343806023 | FASLG | c.515C>G (p.Ser172Cys) c.*85C>G (n.*85C>G) | |
1 | g.172665685C>T | CA343806022 | FASLG | c.515C>T (p.Ser172Phe) c.*85C>T (n.*85C>T) | COSMIC |
1 | g.172665686T>A | CA421944437 | FASLG | c.516T>A (p.Ser172=) c.*86T>A (n.*86T>A) | |
1 | g.172665686T>C | CA421944438 | FASLG | c.516T>C (p.Ser172=) c.*86T>C (n.*86T>C) | |
1 | g.172665686T>G | CA421944439 | FASLG | c.516T>G (p.Ser172=) c.*86T>G (n.*86T>G) | |
1 | g.172665687G>A | CA343806024 | FASLG | c.517G>A (p.Gly173Arg) c.*87G>A (n.*87G>A) | |
1 | g.172665687G>C | CA343806025 | FASLG | c.517G>C (p.Gly173Arg) c.*87G>C (n.*87G>C) | COSMIC |
1 | g.172665687G>T | CA343806026 | FASLG | c.517G>T (p.Gly173Ter) c.*87G>T (n.*87G>T) | |
1 | g.172665688G>A | CA343806027 | FASLG | c.518G>A (p.Gly173Glu) c.*88G>A (n.*88G>A) | |
1 | g.172665688G>C | CA343806028 | FASLG | c.518G>C (p.Gly173Ala) c.*88G>C (n.*88G>C) | |
1 | g.172665688G>T | CA343806029 | FASLG | c.518G>T (p.Gly173Val) c.*88G>T (n.*88G>T) | |
1 | g.172665689A= | CA1207431660 | FASLG | c.519A= (p.Gly173=) c.*89A= (n.*89A=) | |
1 | g.172665689A>C | CA421944440 | FASLG | c.519A>C (p.Gly173=) c.*89A>C (n.*89A>C) | |
1 | g.172665689A>G | CA421944442 | FASLG | c.519A>G (p.Gly173=) c.*89A>G (n.*89A>G) | dbSNP |
1 | g.172665689A>T | CA421944441 | FASLG | c.519A>T (p.Gly173=) c.*89A>T (n.*89A>T) | |
1 | g.172665690G>A | CA343806030 | FASLG | c.520G>A (p.Val174Met) c.*90G>A (n.*90G>A) | |
1 | g.172665690G>C | CA343806031 | FASLG | c.520G>C (p.Val174Leu) c.*90G>C (n.*90G>C) | gnomAD v4 |
1 | g.172665690G>T | CA343806032 | FASLG | c.520G>T (p.Val174Leu) c.*90G>T (n.*90G>T) | |
1 | g.172665691T>A | CA343806033 | FASLG | c.521T>A (p.Val174Glu) c.*91T>A (n.*91T>A) | |
1 | g.172665691T>C | CA343806034 | FASLG | c.521T>C (p.Val174Ala) c.*91T>C (n.*91T>C) | |
1 | g.172665691T>G | CA343806035 | FASLG | c.521T>G (p.Val174Gly) c.*91T>G (n.*91T>G) | |
1 | g.172665692G>A | CA32979641 | FASLG | c.522G>A (p.Val174=) c.*92G>A (n.*92G>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665692G>C | CA421944443 | FASLG | c.522G>C (p.Val174=) c.*92G>C (n.*92G>C) | |
1 | g.172665692G= | CA1143885218 | FASLG | c.522G= (p.Val174=) c.*92G= (n.*92G=) | |
1 | g.172665692G>T | CA421944444 | FASLG | c.522G>T (p.Val174=) c.*92G>T (n.*92G>T) | |
1 | g.172665693A= | CA1207431661 | FASLG | c.523A= (p.Lys175=) c.*93A= (n.*93A=) | |
1 | g.172665693A>C | CA343806036 | FASLG | c.523A>C (p.Lys175Gln) c.*93A>C (n.*93A>C) | gnomAD v4 |
1 | g.172665693A>G | CA343806037 | FASLG | c.523A>G (p.Lys175Glu) c.*93A>G (n.*93A>G) | |
1 | g.172665693A>T | CA343806038 | FASLG | c.523A>T (p.Lys175Ter) c.*93A>T (n.*93A>T) | dbSNP gnomAD v4 |
1 | g.172665694A>C | CA343806039 | FASLG | c.524A>C (p.Lys175Thr) c.*94A>C (n.*94A>C) | |
1 | g.172665694A>G | CA343806040 | FASLG | c.524A>G (p.Lys175Arg) c.*94A>G (n.*94A>G) | |
1 | g.172665694A>T | CA343806041 | FASLG | c.524A>T (p.Lys175Met) c.*94A>T (n.*94A>T) | |
1 | g.172665695G>A | CA421944445 | FASLG | c.525G>A (p.Lys175=) c.*95G>A (n.*95G>A) | dbSNP gnomAD v4 |
1 | g.172665695G>C | CA343806042 | FASLG | c.525G>C (p.Lys175Asn) c.*95G>C (n.*95G>C) | |
1 | g.172665695G= | CA1148725135 | FASLG | c.525G= (p.Lys175=) c.*95G= (n.*95G=) | |
1 | g.172665695G>T | CA1247584 | FASLG | c.525G>T (p.Lys175Asn) c.*95G>T (n.*95G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.172665696T>A | CA343806043 | FASLG | c.526T>A (p.Tyr176Asn) c.*96T>A (n.*96T>A) | gnomAD v4 |
1 | g.172665696T>C | CA343806044 | FASLG | c.526T>C (p.Tyr176His) c.*96T>C (n.*96T>C) | |
1 | g.172665696T>G | CA343806045 | FASLG | c.526T>G (p.Tyr176Asp) c.*96T>G (n.*96T>G) | |
1 | g.172665697A= | CA1207431662 | FASLG | c.527A= (p.Tyr176=) c.*97A= (n.*97A=) | |
1 | g.172665697A>C | CA343806048 | FASLG | c.527A>C (p.Tyr176Ser) c.*97A>C (n.*97A>C) | |
1 | g.172665697A>G | CA343806047 | FASLG | c.527A>G (p.Tyr176Cys) c.*97A>G (n.*97A>G) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665697A>T | CA343806046 | FASLG | c.527A>T (p.Tyr176Phe) c.*97A>T (n.*97A>T) | |
1 | g.172665698T>A | CA343806049 | FASLG | c.528T>A (p.Tyr176Ter) c.*98T>A (n.*98T>A) | |
1 | g.172665698T>C | CA421944446 | FASLG | c.528T>C (p.Tyr176=) c.*98T>C (n.*98T>C) | |
1 | g.172665698T>G | CA343806050 | FASLG | c.528T>G (p.Tyr176Ter) c.*98T>G (n.*98T>G) | |
1 | g.172665698_172665701delinsTAAG | CA1207431663 | FASLG | c.528_531delinsTAAG (p.Tyr176=) c.*98_*101delinsTAAG (n.*98_*101delinsTAAG) | |
1 | g.172665699A>C | CA343806051 | FASLG | c.529A>C (p.Lys177Gln) c.*99A>C (n.*99A>C) | |
1 | g.172665699A>G | CA343806052 | FASLG | c.529A>G (p.Lys177Glu) c.*99A>G (n.*99A>G) | |
1 | g.172665699A>T | CA343806053 | FASLG | c.529A>T (p.Lys177Ter) c.*99A>T (n.*99A>T) | |
1 | g.172665702_172665704del | CA527602096 | FASLG | c.532_534del (p.Lys178del) c.*102_*104del (n.*102_*104del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665700A>C | CA343806054 | FASLG | c.530A>C (p.Lys177Thr) c.*100A>C (n.*100A>C) | |
1 | g.172665700A>G | CA343806055 | FASLG | c.530A>G (p.Lys177Arg) c.*100A>G (n.*100A>G) | |
1 | g.172665700A>T | CA343806056 | FASLG | c.530A>T (p.Lys177Met) c.*100A>T (n.*100A>T) | |
1 | g.172665701G>A | CA421944447 | FASLG | c.531G>A (p.Lys177=) c.*101G>A (n.*101G>A) | |
1 | g.172665701G>C | CA343806057 | FASLG | c.531G>C (p.Lys177Asn) c.*101G>C (n.*101G>C) | dbSNP gnomAD v4 |
1 | g.172665701G= | CA1207431664 | FASLG | c.531G= (p.Lys177=) c.*101G= (n.*101G=) | |
1 | g.172665701G>T | CA343806058 | FASLG | c.531G>T (p.Lys177Asn) c.*101G>T (n.*101G>T) | |
1 | g.172665702A= | CA1207431665 | FASLG | c.532A= (p.Lys178=) c.*102A= (n.*102A=) | |
1 | g.172665702A>C | CA343806059 | FASLG | c.532A>C (p.Lys178Gln) c.*102A>C (n.*102A>C) | |
1 | g.172665702A>G | CA1247585 | FASLG | c.532A>G (p.Lys178Glu) c.*102A>G (n.*102A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.172665702A>T | CA343806060 | FASLG | c.532A>T (p.Lys178Ter) c.*102A>T (n.*102A>T) | |
1 | g.172665703A>C | CA343806061 | FASLG | c.533A>C (p.Lys178Thr) c.*103A>C (n.*103A>C) | |
1 | g.172665703A>G | CA343806063 | FASLG | c.533A>G (p.Lys178Arg) c.*103A>G (n.*103A>G) | |
1 | g.172665703A>T | CA343806062 | FASLG | c.533A>T (p.Lys178Met) c.*103A>T (n.*103A>T) | COSMIC |
1 | g.172665704G>A | CA421944448 | FASLG | c.534G>A (p.Lys178=) c.*104G>A (n.*104G>A) | |
1 | g.172665704G>C | CA343806064 | FASLG | c.534G>C (p.Lys178Asn) c.*104G>C (n.*104G>C) | gnomAD v4 |
1 | g.172665704G= | CA1207431666 | FASLG | c.534G= (p.Lys178=) c.*104G= (n.*104G=) | |
1 | g.172665704G>T | CA343806065 | FASLG | c.534G>T (p.Lys178Asn) c.*104G>T (n.*104G>T) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665705G>A | CA343806066 | FASLG | c.535G>A (p.Gly179Ser) c.*105G>A (n.*105G>A) | |
1 | g.172665705G>C | CA343806067 | FASLG | c.535G>C (p.Gly179Arg) c.*105G>C (n.*105G>C) | |
1 | g.172665705G>T | CA343806068 | FASLG | c.535G>T (p.Gly179Cys) c.*105G>T (n.*105G>T) | |
1 | g.172665706G>A | CA343806069 | FASLG | c.536G>A (p.Gly179Asp) c.*106G>A (n.*106G>A) | gnomAD v4 |
1 | g.172665706G>C | CA343806070 | FASLG | c.536G>C (p.Gly179Ala) c.*106G>C (n.*106G>C) | |
1 | g.172665706G>T | CA343806071 | FASLG | c.536G>T (p.Gly179Val) c.*106G>T (n.*106G>T) | |
1 | g.172665707T>A | CA421944449 | FASLG | c.537T>A (p.Gly179=) c.*107T>A (n.*107T>A) | |
1 | g.172665707T>C | CA421944450 | FASLG | c.537T>C (p.Gly179=) c.*107T>C (n.*107T>C) | ClinVar dbSNP |
1 | g.172665707T>G | CA421944451 | FASLG | c.537T>G (p.Gly179=) c.*107T>G (n.*107T>G) | |
1 | g.172665708G>A | CA343806072 | FASLG | c.538G>A (p.Gly180Ser) c.*108G>A (n.*108G>A) | gnomAD v4 |
1 | g.172665708G>C | CA343806073 | FASLG | c.538G>C (p.Gly180Arg) c.*108G>C (n.*108G>C) | |
1 | g.172665708G>T | CA343806074 | FASLG | c.538G>T (p.Gly180Cys) c.*108G>T (n.*108G>T) | |
1 | g.172665709G>A | CA343806077 | FASLG | c.539G>A (p.Gly180Asp) c.*109G>A (n.*109G>A) | |
1 | g.172665709G>C | CA343806076 | FASLG | c.539G>C (p.Gly180Ala) c.*109G>C (n.*109G>C) | |
1 | g.172665709G>T | CA343806075 | FASLG | c.539G>T (p.Gly180Val) c.*109G>T (n.*109G>T) | |
1 | g.172665710C>A | CA421944452 | FASLG | c.540C>A (p.Gly180=) c.*110C>A (n.*110C>A) | |
1 | g.172665710C= | CA1207431667 | FASLG | c.540C= (p.Gly180=) c.*110C= (n.*110C=) | |
1 | g.172665710C>G | CA32979642 | FASLG | c.540C>G (p.Gly180=) c.*110C>G (n.*110C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665710C>T | CA32979643 | FASLG | c.540C>T (p.Gly180=) c.*110C>T (n.*110C>T) | ClinVar dbSNP |
1 | g.172665711C>A | CA343806079 | FASLG | c.541C>A (p.Leu181Ile) c.*111C>A (n.*111C>A) | gnomAD v4 |
1 | g.172665711C= | CA1207431668 | FASLG | c.541C= (p.Leu181=) c.*111C= (n.*111C=) | |
1 | g.172665711C>G | CA343806078 | FASLG | c.541C>G (p.Leu181Val) c.*111C>G (n.*111C>G) | |
1 | g.172665711C>T | CA1247586 | FASLG | c.541C>T (p.Leu181Phe) c.*111C>T (n.*111C>T) | dbSNP ExAC gnomAD v2 COSMIC |
1 | g.172665712T>A | CA343806080 | FASLG | c.542T>A (p.Leu181His) c.*112T>A (n.*112T>A) | |
1 | g.172665712T>C | CA343806081 | FASLG | c.542T>C (p.Leu181Pro) c.*112T>C (n.*112T>C) | |
1 | g.172665712T>G | CA343806082 | FASLG | c.542T>G (p.Leu181Arg) c.*112T>G (n.*112T>G) | |
1 | g.172665713T>A | CA421944453 | FASLG | c.543T>A (p.Leu181=) c.*113T>A (n.*113T>A) | |
1 | g.172665713T>C | CA421944454 | FASLG | c.543T>C (p.Leu181=) c.*113T>C (n.*113T>C) | |
1 | g.172665713T>G | CA421944455 | FASLG | c.543T>G (p.Leu181=) c.*113T>G (n.*113T>G) | |
1 | g.172665714G>A | CA343806085 | FASLG | c.544G>A (p.Val182Met) c.*114G>A (n.*114G>A) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665714G>C | CA343806084 | FASLG | c.544G>C (p.Val182Leu) c.*114G>C (n.*114G>C) | |
1 | g.172665714G= | CA1207431669 | FASLG | c.544G= (p.Val182=) c.*114G= (n.*114G=) | |
1 | g.172665714G>T | CA343806083 | FASLG | c.544G>T (p.Val182Leu) c.*114G>T (n.*114G>T) | |
1 | g.172665715T>A | CA343806086 | FASLG | c.545T>A (p.Val182Glu) c.*115T>A (n.*115T>A) | |
1 | g.172665715T>C | CA343806087 | FASLG | c.545T>C (p.Val182Ala) c.*115T>C (n.*115T>C) | |
1 | g.172665715T>G | CA1247587 | FASLG | c.545T>G (p.Val182Gly) c.*115T>G (n.*115T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.172665715T= | CA1148451381 | FASLG | c.545T= (p.Val182=) c.*115T= (n.*115T=) | |
1 | g.172665716G>A | CA421944456 | FASLG | c.546G>A (p.Val182=) c.*116G>A (n.*116G>A) | |
1 | g.172665716G>C | CA421944457 | FASLG | c.546G>C (p.Val182=) c.*116G>C (n.*116G>C) | |
1 | g.172665716G>T | CA421944458 | FASLG | c.546G>T (p.Val182=) c.*116G>T (n.*116G>T) | |
1 | g.172665717A>C | CA343806088 | FASLG | c.547A>C (p.Ile183Leu) c.*117A>C (n.*117A>C) | |
1 | g.172665717A>G | CA343806089 | FASLG | c.547A>G (p.Ile183Val) c.*117A>G (n.*117A>G) | gnomAD v4 |
1 | g.172665717A>T | CA343806090 | FASLG | c.547A>T (p.Ile183Phe) c.*117A>T (n.*117A>T) | |
1 | g.172665718T>A | CA343806093 | FASLG | c.548T>A (p.Ile183Asn) c.*118T>A (n.*118T>A) | |
1 | g.172665718T>C | CA343806091 | FASLG | c.548T>C (p.Ile183Thr) c.*118T>C (n.*118T>C) | dbSNP |
1 | g.172665718T>G | CA343806092 | FASLG | c.548T>G (p.Ile183Ser) c.*118T>G (n.*118T>G) | |
1 | g.172665718T= | CA1207431670 | FASLG | c.548T= (p.Ile183=) c.*118T= (n.*118T=) | |
1 | g.172665719C>A | CA421944460 | FASLG | c.549C>A (p.Ile183=) c.*119C>A (n.*119C>A) | |
1 | g.172665719C>G | CA343806094 | FASLG | c.549C>G (p.Ile183Met) c.*119C>G (n.*119C>G) | |
1 | g.172665719C>T | CA421944459 | FASLG | c.549C>T (p.Ile183=) c.*119C>T (n.*119C>T) | |
1 | g.172665720A>C | CA343806095 | FASLG | c.550A>C (p.Asn184His) c.*120A>C (n.*120A>C) | |
1 | g.172665720A>G | CA343806096 | FASLG | c.550A>G (p.Asn184Asp) c.*120A>G (n.*120A>G) | |
1 | g.172665720A>T | CA343806097 | FASLG | c.550A>T (p.Asn184Tyr) c.*120A>T (n.*120A>T) | |
1 | g.172665721A= | CA1207431671 | FASLG | c.551A= (p.Asn184=) c.*121A= (n.*121A=) | |
1 | g.172665721A>C | CA343806098 | FASLG | c.551A>C (p.Asn184Thr) c.*121A>C (n.*121A>C) | gnomAD v4 |
1 | g.172665721A>G | CA32979644 | FASLG | c.551A>G (p.Asn184Ser) c.*121A>G (n.*121A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665721A>T | CA343806099 | FASLG | c.551A>T (p.Asn184Ile) c.*121A>T (n.*121A>T) | |
1 | g.172665722T>A | CA343806100 | FASLG | c.552T>A (p.Asn184Lys) c.*122T>A (n.*122T>A) | COSMIC |
1 | g.172665722T>C | CA1247588 | FASLG | c.552T>C (p.Asn184=) c.*122T>C (n.*122T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665722T>G | CA1247589 | FASLG | c.552T>G (p.Asn184Lys) c.*122T>G (n.*122T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.172665722T= | CA1207431672 | FASLG | c.552T= (p.Asn184=) c.*122T= (n.*122T=) | |
1 | g.172665723G>A | CA343806101 | FASLG | c.553G>A (p.Glu185Lys) c.*123G>A (n.*123G>A) | COSMIC |
1 | g.172665723G>C | CA343806102 | FASLG | c.553G>C (p.Glu185Gln) c.*123G>C (n.*123G>C) | |
1 | g.172665723G>T | CA343806103 | FASLG | c.553G>T (p.Glu185Ter) c.*123G>T (n.*123G>T) | |
1 | g.172665724A>C | CA343806104 | FASLG | c.554A>C (p.Glu185Ala) c.*124A>C (n.*124A>C) | |
1 | g.172665724A>G | CA343806106 | FASLG | c.554A>G (p.Glu185Gly) c.*124A>G (n.*124A>G) | |
1 | g.172665724A>T | CA343806105 | FASLG | c.554A>T (p.Glu185Val) c.*124A>T (n.*124A>T) | |
1 | g.172665725A>C | CA343806107 | FASLG | c.555A>C (p.Glu185Asp) c.*125A>C (n.*125A>C) | |
1 | g.172665725A>G | CA421944461 | FASLG | c.555A>G (p.Glu185=) c.*125A>G (n.*125A>G) | |
1 | g.172665725A>T | CA343806108 | FASLG | c.555A>T (p.Glu185Asp) c.*125A>T (n.*125A>T) | |
1 | g.172665726A>C | CA343806109 | FASLG | c.556A>C (p.Thr186Pro) c.*126A>C (n.*126A>C) | |
1 | g.172665726A>G | CA343806110 | FASLG | c.556A>G (p.Thr186Ala) c.*126A>G (n.*126A>G) | |
1 | g.172665726A>T | CA343806111 | FASLG | c.556A>T (p.Thr186Ser) c.*126A>T (n.*126A>T) | |
1 | g.172665727C>A | CA343806112 | FASLG | c.557C>A (p.Thr186Asn) c.*127C>A (n.*127C>A) | |
1 | g.172665727C= | CA1207431673 | FASLG | c.557C= (p.Thr186=) c.*127C= (n.*127C=) | |
1 | g.172665727C>G | CA343806113 | FASLG | c.557C>G (p.Thr186Ser) c.*127C>G (n.*127C>G) | dbSNP |
1 | g.172665727C>T | CA343806114 | FASLG | c.557C>T (p.Thr186Ile) c.*127C>T (n.*127C>T) | |
1 | g.172665728T>A | CA421944462 | FASLG | c.558T>A (p.Thr186=) c.*128T>A (n.*128T>A) | |
1 | g.172665728T>C | CA421944463 | FASLG | c.558T>C (p.Thr186=) c.*128T>C (n.*128T>C) | |
1 | g.172665728T>G | CA421944464 | FASLG | c.558T>G (p.Thr186=) c.*128T>G (n.*128T>G) | |
1 | g.172665729G>A | CA343806115 | FASLG | c.559G>A (p.Gly187Arg) c.*129G>A (n.*129G>A) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
1 | g.172665729G>C | CA343806116 | FASLG | c.559G>C (p.Gly187Arg) c.*129G>C (n.*129G>C) | |
1 | g.172665729G= | CA1207431674 | FASLG | c.559G= (p.Gly187=) c.*129G= (n.*129G=) | |
1 | g.172665729G>T | CA343806117 | FASLG | c.559G>T (p.Gly187Trp) c.*129G>T (n.*129G>T) | |
1 | g.172665730G>A | CA343806120 | FASLG | c.560G>A (p.Gly187Glu) c.*130G>A (n.*130G>A) | |
1 | g.172665730G>C | CA343806119 | FASLG | c.560G>C (p.Gly187Ala) c.*130G>C (n.*130G>C) | |
1 | g.172665730G>T | CA343806118 | FASLG | c.560G>T (p.Gly187Val) c.*130G>T (n.*130G>T) | |
1 | g.172665731G>A | CA421944465 | FASLG | c.561G>A (p.Gly187=) c.*131G>A (n.*131G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.172665731G>C | CA421944466 | FASLG | c.561G>C (p.Gly187=) c.*131G>C (n.*131G>C) | |
1 | g.172665731G= | CA1207431675 | FASLG | c.561G= (p.Gly187=) c.*131G= (n.*131G=) | |
1 | g.172665731G>T | CA421944467 | FASLG | c.561G>T (p.Gly187=) c.*131G>T (n.*131G>T) | |
1 | g.172665732C>A | CA1247590 | FASLG | c.562C>A (p.Leu188Met) c.*132C>A (n.*132C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665732C= | CA1207431676 | FASLG | c.562C= (p.Leu188=) c.*132C= (n.*132C=) | |
1 | g.172665732C>G | CA1247591 | FASLG | c.562C>G (p.Leu188Val) c.*132C>G (n.*132C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.172665732C>T | CA421944468 | FASLG | c.562C>T (p.Leu188=) c.*132C>T (n.*132C>T) | |
1 | g.172665733T>A | CA343806121 | FASLG | c.563T>A (p.Leu188Gln) c.*133T>A (n.*133T>A) | |
1 | g.172665733T>C | CA343806122 | FASLG | c.563T>C (p.Leu188Pro) c.*133T>C (n.*133T>C) | |
1 | g.172665733T>G | CA343806123 | FASLG | c.563T>G (p.Leu188Arg) c.*133T>G (n.*133T>G) | |
1 | g.172665734G>A | CA421944469 | FASLG | c.564G>A (p.Leu188=) c.*134G>A (n.*134G>A) | dbSNP |
1 | g.172665734G>C | CA421944470 | FASLG | c.564G>C (p.Leu188=) c.*134G>C (n.*134G>C) | |
1 | g.172665734G= | CA1207431677 | FASLG | c.564G= (p.Leu188=) c.*134G= (n.*134G=) | |
1 | g.172665734G>T | CA421944471 | FASLG | c.564G>T (p.Leu188=) c.*134G>T (n.*134G>T) | |
1 | g.172665735T>A | CA343806124 | FASLG | c.565T>A (p.Tyr189Asn) c.*135T>A (n.*135T>A) | |
1 | g.172665735T>C | CA343806125 | FASLG | c.565T>C (p.Tyr189His) c.*135T>C (n.*135T>C) | |
1 | g.172665735T>G | CA343806126 | FASLG | c.565T>G (p.Tyr189Asp) c.*135T>G (n.*135T>G) | |
1 | g.172665736A= | CA1140342297 | FASLG | c.566A= (p.Tyr189=) c.*136A= (n.*136A=) | |
1 | g.172665736A>C | CA32979645 | FASLG | c.566A>C (p.Tyr189Ser) c.*136A>C (n.*136A>C) | dbSNP |
1 | g.172665736A>G | CA343806127 | FASLG | c.566A>G (p.Tyr189Cys) c.*136A>G (n.*136A>G) | gnomAD v4 |
1 | g.172665736A>T | CA343806128 | FASLG | c.566A>T (p.Tyr189Phe) c.*136A>T (n.*136A>T) | |
1 | g.172665737C>A | CA343806129 | FASLG | c.567C>A (p.Tyr189Ter) c.*137C>A (n.*137C>A) | |
1 | g.172665737C>G | CA343806130 | FASLG | c.567C>G (p.Tyr189Ter) c.*137C>G (n.*137C>G) | |
1 | g.172665737C>T | CA421944472 | FASLG | c.567C>T (p.Tyr189=) c.*137C>T (n.*137C>T) | |
1 | g.172665738T>A | CA343806132 | FASLG | c.568T>A (p.Phe190Ile) c.*138T>A (n.*138T>A) | |
1 | g.172665738T>C | CA343806133 | FASLG | c.568T>C (p.Phe190Leu) c.*138T>C (n.*138T>C) | gnomAD v4 |
1 | g.172665738T>G | CA343806131 | FASLG | c.568T>G (p.Phe190Val) c.*138T>G (n.*138T>G) | |
1 | g.172665739T>A | CA343806134 | FASLG | c.569T>A (p.Phe190Tyr) c.*139T>A (n.*139T>A) | |
1 | g.172665739T>C | CA343806136 | FASLG | c.569T>C (p.Phe190Ser) c.*139T>C (n.*139T>C) | |
1 | g.172665739T>G | CA343806135 | FASLG | c.569T>G (p.Phe190Cys) c.*139T>G (n.*139T>G) | |
1 | g.172665740T>A | CA343806137 | FASLG | c.570T>A (p.Phe190Leu) c.*140T>A (n.*140T>A) | |
1 | g.172665740T>C | CA421944473 | FASLG | c.570T>C (p.Phe190=) c.*140T>C (n.*140T>C) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.172665740T>G | CA343806138 | FASLG | c.570T>G (p.Phe190Leu) c.*140T>G (n.*140T>G) | |
1 | g.172665740T= | CA1207431678 | FASLG | c.570T= (p.Phe190=) c.*140T= (n.*140T=) | |
1 | g.172665741G>A | CA343806139 | FASLG | c.571G>A (p.Val191Ile) c.*141G>A (n.*141G>A) | |
1 | g.172665741G>C | CA343806140 | FASLG | c.571G>C (p.Val191Leu) c.*141G>C (n.*141G>C) | |
1 | g.172665741G>T | CA343806141 | FASLG | c.571G>T (p.Val191Leu) c.*141G>T (n.*141G>T) | |
1 | g.172665746_172665757del | CA2580061374 | FASLG | c.576_587del (p.Ser193_Tyr196del) c.*146_*157del (n.*146_*157del) | ClinVar |
1 | g.172665742T>A | CA343806142 | FASLG | c.572T>A (p.Val191Glu) c.*142T>A (n.*142T>A) | |
1 | g.172665742T>C | CA343806143 | FASLG | c.572T>C (p.Val191Ala) c.*142T>C (n.*142T>C) | |
1 | g.172665742T>G | CA343806144 | FASLG | c.572T>G (p.Val191Gly) c.*142T>G (n.*142T>G) | |
1 | g.172665743A>C | CA421944476 | FASLG | c.573A>C (p.Val191=) c.*143A>C (n.*143A>C) | |
1 | g.172665743A>G | CA421944475 | FASLG | c.573A>G (p.Val191=) c.*143A>G (n.*143A>G) | |
1 | g.172665743A>T | CA421944474 | FASLG | c.573A>T (p.Val191=) c.*143A>T (n.*143A>T) | |
1 | g.172665744T>A | CA343806145 | FASLG | c.574T>A (p.Tyr192Asn) c.*144T>A (n.*144T>A) | |
1 | g.172665744T>C | CA343806146 | FASLG | c.574T>C (p.Tyr192His) c.*144T>C (n.*144T>C) | |
1 | g.172665744T>G | CA343806147 | FASLG | c.574T>G (p.Tyr192Asp) c.*144T>G (n.*144T>G) | |
1 | g.172665745A>C | CA343806150 | FASLG | c.575A>C (p.Tyr192Ser) c.*145A>C (n.*145A>C) | |
1 | g.172665745A>G | CA343806149 | FASLG | c.575A>G (p.Tyr192Cys) c.*145A>G (n.*145A>G) | |
1 | g.172665745A>T | CA343806148 | FASLG | c.575A>T (p.Tyr192Phe) c.*145A>T (n.*145A>T) | COSMIC |
1 | g.172665746T>A | CA343806151 | FASLG | c.576T>A (p.Tyr192Ter) c.*146T>A (n.*146T>A) | |
1 | g.172665746T>C | CA421944477 | FASLG | c.576T>C (p.Tyr192=) c.*146T>C (n.*146T>C) | |
1 | g.172665746T>G | CA343806152 | FASLG | c.576T>G (p.Tyr192Ter) c.*146T>G (n.*146T>G) | |
1 | g.172665747T>A | CA343806153 | FASLG | c.577T>A (p.Ser193Thr) c.*147T>A (n.*147T>A) | |
1 | g.172665747T>C | CA343806154 | FASLG | c.577T>C (p.Ser193Pro) c.*147T>C (n.*147T>C) | |
1 | g.172665747T>G | CA343806155 | FASLG | c.577T>G (p.Ser193Ala) c.*147T>G (n.*147T>G) | |
1 | g.172665748C>A | CA343806156 | FASLG | c.578C>A (p.Ser193Tyr) c.*148C>A (n.*148C>A) | |
1 | g.172665748C>G | CA343806157 | FASLG | c.578C>G (p.Ser193Cys) c.*148C>G (n.*148C>G) | |
1 | g.172665748C>T | CA343806158 | FASLG | c.578C>T (p.Ser193Phe) c.*148C>T (n.*148C>T) | |
1 | g.172665749C>A | CA421944478 | FASLG | c.579C>A (p.Ser193=) c.*149C>A (n.*149C>A) | gnomAD v4 |
1 | g.172665749C= | CA1144030463 | FASLG | c.579C= (p.Ser193=) c.*149C= (n.*149C=) | |
1 | g.172665749C>G | CA421944479 | FASLG | c.579C>G (p.Ser193=) c.*149C>G (n.*149C>G) | |
1 | g.172665749C>T | CA32979646 | FASLG | c.579C>T (p.Ser193=) c.*149C>T (n.*149C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.172665750A>C | CA343806159 | FASLG | c.580A>C (p.Lys194Gln) c.*150A>C (n.*150A>C) | |
1 | g.172665750A>G | CA343806160 | FASLG | c.580A>G (p.Lys194Glu) c.*150A>G (n.*150A>G) | |
1 | g.172665750A>T | CA343806161 | FASLG | c.580A>T (p.Lys194Ter) c.*150A>T (n.*150A>T) | |
1 | g.172665751A>C | CA343806164 | FASLG | c.581A>C (p.Lys194Thr) c.*151A>C (n.*151A>C) | |
1 | g.172665751A>G | CA343806163 | FASLG | c.581A>G (p.Lys194Arg) c.*151A>G (n.*151A>G) | |
1 | g.172665751A>T | CA343806162 | FASLG | c.581A>T (p.Lys194Ile) c.*151A>T (n.*151A>T) | |
1 | g.172665752A= | CA1207431679 | FASLG | c.582A= (p.Lys194=) c.*152A= (n.*152A=) | |
1 | g.172665752A>C | CA343806166 | FASLG | c.582A>C (p.Lys194Asn) c.*152A>C (n.*152A>C) | |
1 | g.172665752A>G | CA421944480 | FASLG | c.582A>G (p.Lys194=) c.*152A>G (n.*152A>G) | dbSNP |
1 | g.172665752A>T | CA343806165 | FASLG | c.582A>T (p.Lys194Asn) c.*152A>T (n.*152A>T) | |
1 | g.172665753G>A | CA343806167 | FASLG | c.583G>A (p.Val195Ile) c.*153G>A (n.*153G>A) | gnomAD v4 |
1 | g.172665753G>C | CA343806168 | FASLG | c.583G>C (p.Val195Leu) c.*153G>C (n.*153G>C) | |
1 | g.172665753G>T | CA343806169 | FASLG | c.583G>T (p.Val195Leu) c.*153G>T (n.*153G>T) | COSMIC |