Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.111401046C>A | CA414245915 | DCX | c.649G>T (p.Ala217Ser) c.892G>T (p.Ala298Ser) c.867G>T n.889G>T | |
X | g.111401046C= | CA2451697213 | DCX | c.649G= (p.Ala217=) c.892G= (p.Ala298=) c.867G= n.889G= | |
X | g.111401046C>G | CA414245916 | DCX | c.649G>C (p.Ala217Pro) c.892G>C (p.Ala298Pro) c.867G>C n.889G>C | |
X | g.111401046C>T | CA414245917 | DCX | c.649G>A (p.Ala217Thr) c.892G>A (p.Ala298Thr) c.867G>A n.889G>A | dbSNP gnomAD v2 gnomAD v4 |
X | g.111401047T>A | CA414245919 | DCX | c.648A>T (p.Glu216Asp) c.891A>T (p.Glu297Asp) c.866A>T n.888A>T | |
X | g.111401047T>C | CA518113953 | DCX | c.648A>G (p.Glu216=) c.891A>G (p.Glu297=) c.866A>G n.888A>G | |
X | g.111401047T>G | CA414245918 | DCX | c.648A>C (p.Glu216Asp) c.891A>C (p.Glu297Asp) c.866A>C n.888A>C | |
X | g.111401048T>A | CA414245920 | DCX | c.647A>T (p.Glu216Val) c.890A>T (p.Glu297Val) c.865A>T n.887A>T | |
X | g.111401048T>C | CA414245921 | DCX | c.647A>G (p.Glu216Gly) c.890A>G (p.Glu297Gly) c.865A>G n.887A>G | |
X | g.111401048T>G | CA414245922 | DCX | c.647A>C (p.Glu216Ala) c.890A>C (p.Glu297Ala) c.865A>C n.887A>C | |
X | g.111401049C>A | CA414245923 | DCX | c.646G>T (p.Glu216Ter) c.889G>T (p.Glu297Ter) c.864G>T n.886G>T | |
X | g.111401049C>G | CA414245924 | DCX | c.646G>C (p.Glu216Gln) c.889G>C (p.Glu297Gln) c.864G>C n.886G>C | |
X | g.111401049C>T | CA414245925 | DCX | c.646G>A (p.Glu216Lys) c.889G>A (p.Glu297Lys) c.864G>A n.886G>A | |
X | g.111401050T>A | CA518113954 | DCX | c.645A>T (p.Thr215=) c.888A>T (p.Thr296=) c.863A>T n.885A>T | |
X | g.111401050T>C | CA518113955 | DCX | c.645A>G (p.Thr215=) c.888A>G (p.Thr296=) c.863A>G n.885A>G | |
X | g.111401050T>G | CA518113956 | DCX | c.645A>C (p.Thr215=) c.888A>C (p.Thr296=) c.863A>C n.885A>C | |
X | g.111401051G>A | CA414245926 | DCX | c.644C>T (p.Thr215Ile) c.887C>T (p.Thr296Ile) c.862C>T n.884C>T | |
X | g.111401051G>C | CA414245927 | DCX | c.644C>G (p.Thr215Arg) c.887C>G (p.Thr296Arg) c.862C>G n.884C>G | |
X | g.111401051G>T | CA414245928 | DCX | c.644C>A (p.Thr215Lys) c.887C>A (p.Thr296Lys) c.862C>A n.884C>A | |
X | g.111401055_111401063del | CA2837994656 | DCX | c.636_644del (p.Asp213_Thr215del) c.879_887del (p.Asp294_Thr296del) c.854_862del n.876_884del | |
X | g.111401052T>A | CA414245929 | DCX | c.643A>T (p.Thr215Ser) c.886A>T (p.Thr296Ser) c.861A>T n.883A>T | |
X | g.111401052T>C | CA414245930 | DCX | c.643A>G (p.Thr215Ala) c.886A>G (p.Thr296Ala) c.861A>G n.883A>G | COSMIC COSMIC |
X | g.111401052T>G | CA414245931 | DCX | c.643A>C (p.Thr215Pro) c.886A>C (p.Thr296Pro) c.861A>C n.883A>C | |
X | g.111401053G>A | CA518113957 | DCX | c.642C>T (p.Ile214=) c.885C>T (p.Ile295=) c.860C>T n.882C>T | |
X | g.111401053G>C | CA414245932 | DCX | c.642C>G (p.Ile214Met) c.885C>G (p.Ile295Met) c.860C>G n.882C>G | |
X | g.111401053G>T | CA518113958 | DCX | c.642C>A (p.Ile214=) c.885C>A (p.Ile295=) c.860C>A n.882C>A | |
X | g.111401054A= | CA2451697214 | DCX | c.641T= (p.Ile214=) c.884T= (p.Ile295=) c.859T= n.881T= | |
X | g.111401054A>C | CA414245934 | DCX | c.641T>G (p.Ile214Ser) c.884T>G (p.Ile295Ser) c.859T>G n.881T>G | |
X | g.111401054A>G | CA172041 | DCX | c.641T>C (p.Ile214Thr) c.884T>C (p.Ile295Thr) c.859T>C n.881T>C | ClinVar dbSNP |
X | g.111401054A>T | CA414245933 | DCX | c.641T>A (p.Ile214Asn) c.884T>A (p.Ile295Asn) c.859T>A n.881T>A | |
X | g.111401055T>A | CA414245935 | DCX | c.640A>T (p.Ile214Phe) c.883A>T (p.Ile295Phe) c.858A>T n.880A>T | |
X | g.111401055T>C | CA414245936 | DCX | c.640A>G (p.Ile214Val) c.883A>G (p.Ile295Val) c.858A>G n.880A>G | |
X | g.111401055T>G | CA414245937 | DCX | c.640A>C (p.Ile214Leu) c.883A>C (p.Ile295Leu) c.858A>C n.880A>C | |
X | g.111401056A>C | CA414245938 | DCX | c.639T>G (p.Asp213Glu) c.882T>G (p.Asp294Glu) c.857T>G n.879T>G | |
X | g.111401056A>G | CA518113959 | DCX | c.639T>C (p.Asp213=) c.882T>C (p.Asp294=) c.857T>C n.879T>C | |
X | g.111401056A>T | CA414245939 | DCX | c.639T>A (p.Asp213Glu) c.882T>A (p.Asp294Glu) c.857T>A n.879T>A | |
X | g.111401057T>A | CA414245942 | DCX | c.638A>T (p.Asp213Val) c.881A>T (p.Asp294Val) c.856A>T n.878A>T | |
X | g.111401057T>C | CA414245941 | DCX | c.638A>G (p.Asp213Gly) c.881A>G (p.Asp294Gly) c.856A>G n.878A>G | |
X | g.111401057T>G | CA414245940 | DCX | c.638A>C (p.Asp213Ala) c.881A>C (p.Asp294Ala) c.856A>C n.878A>C | |
X | g.111401058C>A | CA414245943 | DCX | c.637G>T (p.Asp213Tyr) c.880G>T (p.Asp294Tyr) c.855G>T n.877G>T | |
X | g.111401058C>G | CA414245944 | DCX | c.637G>C (p.Asp213His) c.880G>C (p.Asp294His) c.855G>C n.877G>C | |
X | g.111401058C>T | CA414245945 | DCX | c.637G>A (p.Asp213Asn) c.880G>A (p.Asp294Asn) c.855G>A n.877G>A | |
X | g.111401059A>C | CA518113960 | DCX | c.636T>G (p.Thr212=) c.879T>G (p.Thr293=) c.854T>G n.876T>G | |
X | g.111401059A>G | CA518113961 | DCX | c.636T>C (p.Thr212=) c.879T>C (p.Thr293=) c.854T>C n.876T>C | |
X | g.111401059A>T | CA518113962 | DCX | c.636T>A (p.Thr212=) c.879T>A (p.Thr293=) c.854T>A n.876T>A | |
X | g.111401060G>A | CA414245946 | DCX | c.635C>T (p.Thr212Ile) c.878C>T (p.Thr293Ile) c.853C>T n.875C>T | |
X | g.111401060G>C | CA414245947 | DCX | c.635C>G (p.Thr212Ser) c.878C>G (p.Thr293Ser) c.853C>G n.875C>G | |
X | g.111401060G>T | CA414245948 | DCX | c.635C>A (p.Thr212Asn) c.878C>A (p.Thr293Asn) c.853C>A n.875C>A | |
X | g.111401061T>A | CA414245949 | DCX | c.634A>T (p.Thr212Ser) c.877A>T (p.Thr293Ser) c.852A>T n.874A>T | |
X | g.111401061T>C | CA414245951 | DCX | c.634A>G (p.Thr212Ala) c.877A>G (p.Thr293Ala) c.852A>G n.874A>G | |
X | g.111401061T>G | CA414245950 | DCX | c.634A>C (p.Thr212Pro) c.877A>C (p.Thr293Pro) c.852A>C n.874A>C | |
X | g.111401062G>A | CA518113963 | DCX | c.633C>T (p.Leu211=) c.876C>T (p.Leu292=) c.851C>T n.873C>T | |
X | g.111401062G>C | CA518113965 | DCX | c.633C>G (p.Leu211=) c.876C>G (p.Leu292=) c.851C>G n.873C>G | COSMIC COSMIC |
X | g.111401062G>T | CA518113964 | DCX | c.633C>A (p.Leu211=) c.876C>A (p.Leu292=) c.851C>A n.873C>A | |
X | g.111401063A>C | CA414245952 | DCX | c.632T>G (p.Leu211Arg) c.875T>G (p.Leu292Arg) c.850T>G n.872T>G | |
X | g.111401063A>G | CA414245953 | DCX | c.632T>C (p.Leu211Pro) c.875T>C (p.Leu292Pro) c.850T>C n.872T>C | |
X | g.111401063A>T | CA414245954 | DCX | c.632T>A (p.Leu211His) c.875T>A (p.Leu292His) c.850T>A n.872T>A | |
X | g.111401064G>A | CA414245955 | DCX | c.631C>T (p.Leu211Phe) c.874C>T (p.Leu292Phe) c.849C>T n.871C>T | |
X | g.111401064G>C | CA414245956 | DCX | c.631C>G (p.Leu211Val) c.874C>G (p.Leu292Val) c.849C>G n.871C>G | |
X | g.111401064G>T | CA414245957 | DCX | c.631C>A (p.Leu211Ile) c.874C>A (p.Leu292Ile) c.849C>A n.871C>A | COSMIC |
X | g.111401065G>A | CA518113966 | DCX | c.630C>T (p.Val210=) c.873C>T (p.Val291=) c.848C>T n.870C>T | |
X | g.111401065G>C | CA518113967 | DCX | c.630C>G (p.Val210=) c.873C>G (p.Val291=) c.848C>G n.870C>G | |
X | g.111401065G>T | CA518113968 | DCX | c.630C>A (p.Val210=) c.873C>A (p.Val291=) c.848C>A n.870C>A | |
X | g.111401066A= | CA2451697215 | DCX | c.629T= (p.Val210=) c.872T= (p.Val291=) c.847T= n.869T= | |
X | g.111401066A>C | CA414245958 | DCX | c.629T>G (p.Val210Gly) c.872T>G (p.Val291Gly) c.847T>G n.869T>G | |
X | g.111401066A>G | CA10493318 | DCX | c.629T>C (p.Val210Ala) c.872T>C (p.Val291Ala) c.847T>C n.869T>C | dbSNP ExAC |
X | g.111401066A>T | CA414245959 | DCX | c.629T>A (p.Val210Asp) c.872T>A (p.Val291Asp) c.847T>A n.869T>A | |
X | g.111401067del | CA2573055069 | DCX | c.628del (p.Val210SerfsTer27) c.871del (p.Val291SerfsTer27) c.846del n.868del | ClinVar dbSNP |
X | g.111401067C>A | CA172038 | DCX | c.628G>T (p.Val210Phe) c.871G>T (p.Val291Phe) c.846G>T n.868G>T | ClinVar dbSNP |
X | g.111401067C= | CA2451697216 | DCX | c.628G= (p.Val210=) c.871G= (p.Val291=) c.846G= n.868G= | |
X | g.111401067C>G | CA414245960 | DCX | c.628G>C (p.Val210Leu) c.871G>C (p.Val291Leu) c.846G>C n.868G>C | |
X | g.111401067C>T | CA414245961 | DCX | c.628G>A (p.Val210Ile) c.871G>A (p.Val291Ile) c.846G>A n.868G>A | dbSNP gnomAD v4 |
X | g.111401068T>A | CA414245962 | DCX | c.627A>T (p.Gln209His) c.870A>T (p.Gln290His) c.845A>T n.867A>T | |
X | g.111401068T>C | CA518113969 | DCX | c.627A>G (p.Gln209=) c.870A>G (p.Gln290=) c.845A>G n.867A>G | |
X | g.111401068T>G | CA414245963 | DCX | c.627A>C (p.Gln209His) c.870A>C (p.Gln290His) c.845A>C n.867A>C | ClinVar |
X | g.111401069T>A | CA414245964 | DCX | c.626A>T (p.Gln209Leu) c.869A>T (p.Gln290Leu) c.844A>T n.866A>T | |
X | g.111401069T>C | CA414245966 | DCX | c.626A>G (p.Gln209Arg) c.869A>G (p.Gln290Arg) c.844A>G n.866A>G | |
X | g.111401069T>G | CA414245965 | DCX | c.626A>C (p.Gln209Pro) c.869A>C (p.Gln290Pro) c.844A>C n.866A>C | |
X | g.111401070G>A | CA414245967 | DCX | c.625C>T (p.Gln209Ter) c.868C>T (p.Gln290Ter) c.843C>T n.865C>T | |
X | g.111401070G>C | CA414245969 | DCX | c.625C>G (p.Gln209Glu) c.868C>G (p.Gln290Glu) c.843C>G n.865C>G | |
X | g.111401070G>T | CA414245968 | DCX | c.625C>A (p.Gln209Lys) c.868C>A (p.Gln290Lys) c.843C>A n.865C>A | |
X | g.111401071C>A | CA414245970 | DCX | c.624G>T (p.Glu208Asp) c.867G>T (p.Glu289Asp) c.842G>T n.864G>T | |
X | g.111401071C>G | CA414245971 | DCX | c.624G>C (p.Glu208Asp) c.867G>C (p.Glu289Asp) c.842G>C n.864G>C | |
X | g.111401071C>T | CA518113970 | DCX | c.624G>A (p.Glu208=) c.867G>A (p.Glu289=) c.842G>A n.864G>A | |
X | g.111401072T>A | CA414245972 | DCX | c.623A>T (p.Glu208Val) c.866A>T (p.Glu289Val) c.841A>T n.863A>T | |
X | g.111401072T>C | CA414245973 | DCX | c.623A>G (p.Glu208Gly) c.866A>G (p.Glu289Gly) c.841A>G n.863A>G | |
X | g.111401072T>G | CA414245974 | DCX | c.623A>C (p.Glu208Ala) c.866A>C (p.Glu289Ala) c.841A>C n.863A>C | |
X | g.111401073C>A | CA414245975 | DCX | c.622G>T (p.Glu208Ter) c.865G>T (p.Glu289Ter) c.840G>T n.862G>T | |
X | g.111401073C>G | CA414245976 | DCX | c.622G>C (p.Glu208Gln) c.865G>C (p.Glu289Gln) c.840G>C n.862G>C | COSMIC COSMIC |
X | g.111401073C>T | CA414245977 | DCX | c.622G>A (p.Glu208Lys) c.865G>A (p.Glu289Lys) c.840G>A n.862G>A | |
X | g.111401074A>C | CA414245978 | DCX | c.621T>G (p.Phe207Leu) c.864T>G (p.Phe288Leu) c.839T>G n.861T>G | |
X | g.111401074A>G | CA518113971 | DCX | c.621T>C (p.Phe207=) c.864T>C (p.Phe288=) c.839T>C n.861T>C | |
X | g.111401074A>T | CA414245979 | DCX | c.621T>A (p.Phe207Leu) c.864T>A (p.Phe288Leu) c.839T>A n.861T>A | |
X | g.111401075A>C | CA414245982 | DCX | c.620T>G (p.Phe207Cys) c.863T>G (p.Phe288Cys) c.838T>G n.860T>G | |
X | g.111401075A>G | CA414245981 | DCX | c.620T>C (p.Phe207Ser) c.863T>C (p.Phe288Ser) c.838T>C n.860T>C | |
X | g.111401075A>T | CA414245980 | DCX | c.620T>A (p.Phe207Tyr) c.863T>A (p.Phe288Tyr) c.838T>A n.860T>A | |
X | g.111401076A>C | CA414245983 | DCX | c.619T>G (p.Phe207Val) c.862T>G (p.Phe288Val) c.837T>G n.859T>G | |
X | g.111401076A>G | CA414245984 | DCX | c.619T>C (p.Phe207Leu) c.862T>C (p.Phe288Leu) c.837T>C n.859T>C | |
X | g.111401076A>T | CA414245985 | DCX | c.619T>A (p.Phe207Ile) c.862T>A (p.Phe288Ile) c.837T>A n.859T>A | |
X | g.111401077A>C | CA518113972 | DCX | c.618T>G (p.Ser206=) c.861T>G (p.Ser287=) c.836T>G n.858T>G | |
X | g.111401077A>G | CA518113973 | DCX | c.618T>C (p.Ser206=) c.861T>C (p.Ser287=) c.836T>C n.858T>C | |
X | g.111401077A>T | CA518113974 | DCX | c.618T>A (p.Ser206=) c.861T>A (p.Ser287=) c.836T>A n.858T>A | |
X | g.111401078G>A | CA414245986 | DCX | c.617C>T (p.Ser206Phe) c.860C>T (p.Ser287Phe) c.835C>T n.857C>T | |
X | g.111401078G>C | CA414245987 | DCX | c.617C>G (p.Ser206Cys) c.860C>G (p.Ser287Cys) c.835C>G n.857C>G | |
X | g.111401078G>T | CA414245988 | DCX | c.617C>A (p.Ser206Tyr) c.860C>A (p.Ser287Tyr) c.835C>A n.857C>A | |
X | g.111401079A>C | CA414245989 | DCX | c.616T>G (p.Ser206Ala) c.859T>G (p.Ser287Ala) c.834T>G n.856T>G | |
X | g.111401079A>G | CA414245990 | DCX | c.616T>C (p.Ser206Pro) c.859T>C (p.Ser287Pro) c.834T>C n.856T>C | |
X | g.111401079A>T | CA414245991 | DCX | c.616T>A (p.Ser206Thr) c.859T>A (p.Ser287Thr) c.834T>A n.856T>A | |
X | g.111401080G>A | CA518113975 | DCX | c.615C>T (p.His205=) c.858C>T (p.His286=) c.833C>T n.855C>T | |
X | g.111401080G>C | CA414245992 | DCX | c.615C>G (p.His205Gln) c.858C>G (p.His286Gln) c.833C>G n.855C>G | |
X | g.111401080G>T | CA414245993 | DCX | c.615C>A (p.His205Gln) c.858C>A (p.His286Gln) c.833C>A n.855C>A | |
X | g.111401081T>A | CA172035 | DCX | c.614A>T (p.His205Leu) c.857A>T (p.His286Leu) c.832A>T n.854A>T | ClinVar dbSNP |
X | g.111401081T>C | CA414245995 | DCX | c.614A>G (p.His205Arg) c.857A>G (p.His286Arg) c.832A>G n.854A>G | |
X | g.111401081T>G | CA414245994 | DCX | c.614A>C (p.His205Pro) c.857A>C (p.His286Pro) c.832A>C n.854A>C | |
X | g.111401081T= | CA2451697217 | DCX | c.614A= (p.His205=) c.857A= (p.His286=) c.832A= n.854A= | |
X | g.111401082G>A | CA414245996 | DCX | c.613C>T (p.His205Tyr) c.856C>T (p.His286Tyr) c.831C>T n.853C>T | |
X | g.111401082G>C | CA414245997 | DCX | c.613C>G (p.His205Asp) c.856C>G (p.His286Asp) c.831C>G n.853C>G | ClinVar |
X | g.111401082G>T | CA414245998 | DCX | c.613C>A (p.His205Asn) c.856C>A (p.His286Asn) c.831C>A n.853C>A | COSMIC |
X | g.111401083G>A | CA518113976 | DCX | c.612C>T (p.Ala204=) c.855C>T (p.Ala285=) c.830C>T n.852C>T | |
X | g.111401083G>C | CA518113977 | DCX | c.612C>G (p.Ala204=) c.855C>G (p.Ala285=) c.830C>G n.852C>G | |
X | g.111401083G>T | CA518113978 | DCX | c.612C>A (p.Ala204=) c.855C>A (p.Ala285=) c.830C>A n.852C>A | |
X | g.111401084G>A | CA414245999 | DCX | c.611C>T (p.Ala204Val) c.854C>T (p.Ala285Val) c.829C>T n.851C>T | gnomAD v4 |
X | g.111401084G>C | CA414246000 | DCX | c.611C>G (p.Ala204Gly) c.854C>G (p.Ala285Gly) c.829C>G n.851C>G | |
X | g.111401084G= | CA2451697218 | DCX | c.611C= (p.Ala204=) c.854C= (p.Ala285=) c.829C= n.851C= | |
X | g.111401084G>T | CA172032 | DCX | c.611C>A (p.Ala204Asp) c.854C>A (p.Ala285Asp) c.829C>A n.851C>A | ClinVar dbSNP |
X | g.111401085C>A | CA414246001 | DCX | c.610G>T (p.Ala204Ser) c.853G>T (p.Ala285Ser) c.828G>T n.850G>T | |
X | g.111401085C>G | CA414246002 | DCX | c.610G>C (p.Ala204Pro) c.853G>C (p.Ala285Pro) c.828G>C n.850G>C | |
X | g.111401085C>T | CA414246003 | DCX | c.610G>A (p.Ala204Thr) c.853G>A (p.Ala285Thr) c.828G>A n.850G>A | gnomAD v4 |
X | g.111401086T>A | CA518113979 | DCX | c.609A>T (p.Thr203=) c.852A>T (p.Thr284=) c.827A>T n.849A>T | |
X | g.111401086T>C | CA518113980 | DCX | c.609A>G (p.Thr203=) c.852A>G (p.Thr284=) c.827A>G n.849A>G | |
X | g.111401086T>G | CA518113981 | DCX | c.609A>C (p.Thr203=) c.852A>C (p.Thr284=) c.827A>C n.849A>C | |
X | g.111401087G>A | CA414246004 | DCX | c.608C>T (p.Thr203Ile) c.851C>T (p.Thr284Ile) c.826C>T n.848C>T | |
X | g.111401087G>C | CA121598 | DCX | c.608C>G (p.Thr203Arg) c.851C>G (p.Thr284Arg) c.826C>G n.848C>G | ClinVar dbSNP |
X | g.111401087G= | CA2451697219 | DCX | c.608C= (p.Thr203=) c.851C= (p.Thr284=) c.826C= n.848C= | |
X | g.111401087G>T | CA172029 | DCX | c.608C>A (p.Thr203Lys) c.851C>A (p.Thr284Lys) c.826C>A n.848C>A | ClinVar dbSNP |
X | g.111401088T>A | CA414246006 | DCX | c.607A>T (p.Thr203Ser) c.850A>T (p.Thr284Ser) c.825A>T n.847A>T | |
X | g.111401088T>C | CA172026 | DCX | c.607A>G (p.Thr203Ala) c.850A>G (p.Thr284Ala) c.825A>G n.847A>G | ClinVar dbSNP |
X | g.111401088T>G | CA414246005 | DCX | c.607A>C (p.Thr203Pro) c.850A>C (p.Thr284Pro) c.825A>C n.847A>C | |
X | g.111401088T= | CA2451697220 | DCX | c.607A= (p.Thr203=) c.850A= (p.Thr284=) c.825A= n.847A= | |
X | g.111401092_111401094del | CA2580612460 | DCX | c.605_607del (p.Lys202del) c.848_850del (p.Lys283del) c.823_825del n.845_847del | ClinVar |
X | g.111401089C>A | CA414246007 | DCX | c.606G>T (p.Lys202Asn) c.849G>T (p.Lys283Asn) c.824G>T n.846G>T | |
X | g.111401089C= | CA2451697221 | DCX | c.606G= (p.Lys202=) c.849G= (p.Lys283=) c.824G= n.846G= | |
X | g.111401089C>G | CA414246008 | DCX | c.606G>C (p.Lys202Asn) c.849G>C (p.Lys283Asn) c.824G>C n.846G>C | |
X | g.111401089C>T | CA334420246 | DCX | c.606G>A (p.Lys202=) c.849G>A (p.Lys283=) c.824G>A n.846G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
X | g.111401090T>A | CA414246009 | DCX | c.605A>T (p.Lys202Met) c.848A>T (p.Lys283Met) c.823A>T n.845A>T | |
X | g.111401090T>C | CA414246010 | DCX | c.605A>G (p.Lys202Arg) c.848A>G (p.Lys283Arg) c.823A>G n.845A>G | |
X | g.111401090T>G | CA414246011 | DCX | c.605A>C (p.Lys202Thr) c.848A>C (p.Lys283Thr) c.823A>C n.845A>C | |
X | g.111401091T>A | CA414246014 | DCX | c.604A>T (p.Lys202Ter) c.847A>T (p.Lys283Ter) c.822A>T n.844A>T | |
X | g.111401091T>C | CA414246012 | DCX | c.604A>G (p.Lys202Glu) c.847A>G (p.Lys283Glu) c.822A>G n.844A>G | ClinVar |
X | g.111401091T>G | CA414246013 | DCX | c.604A>C (p.Lys202Gln) c.847A>C (p.Lys283Gln) c.822A>C n.844A>C | |
X | g.111401092C>A | CA414246015 | DCX | c.603G>T (p.Lys201Asn) c.846G>T (p.Lys282Asn) c.821G>T n.843G>T | |
X | g.111401092C>G | CA414246016 | DCX | c.603G>C (p.Lys201Asn) c.846G>C (p.Lys282Asn) c.821G>C n.843G>C | |
X | g.111401092C>T | CA518113982 | DCX | c.603G>A (p.Lys201=) c.846G>A (p.Lys282=) c.821G>A n.843G>A | gnomAD v4 COSMIC COSMIC |
X | g.111401093T>A | CA414246017 | DCX | c.602A>T (p.Lys201Met) c.845A>T (p.Lys282Met) c.820A>T n.842A>T | |
X | g.111401093T>C | CA414246018 | DCX | c.602A>G (p.Lys201Arg) c.845A>G (p.Lys282Arg) c.820A>G n.842A>G | |
X | g.111401093T>G | CA414246019 | DCX | c.602A>C (p.Lys201Thr) c.845A>C (p.Lys282Thr) c.820A>C n.842A>C | |
X | g.111401094T>A | CA414246022 | DCX | c.601A>T (p.Lys201Ter) c.844A>T (p.Lys282Ter) c.819A>T n.841A>T | ClinVar dbSNP |
X | g.111401094T>C | CA414246021 | DCX | c.601A>G (p.Lys201Glu) c.844A>G (p.Lys282Glu) c.819A>G n.841A>G | |
X | g.111401094T>G | CA414246020 | DCX | c.601A>C (p.Lys201Gln) c.844A>C (p.Lys282Gln) c.819A>C n.841A>C | |
X | g.111401094T= | CA2451697222 | DCX | c.601A= (p.Lys201=) c.844A= (p.Lys282=) c.819A= n.841A= | |
X | g.111401095G>A | CA518113983 | DCX | c.600C>T (p.Asn200=) c.843C>T (p.Asn281=) c.818C>T n.840C>T | |
X | g.111401095G>C | CA414246023 | DCX | c.600C>G (p.Asn200Lys) c.843C>G (p.Asn281Lys) c.818C>G n.840C>G | |
X | g.111401095G>T | CA414246024 | DCX | c.600C>A (p.Asn200Lys) c.843C>A (p.Asn281Lys) c.818C>A n.840C>A | |
X | g.111401096T>A | CA414246025 | DCX | c.599A>T (p.Asn200Ile) c.842A>T (p.Asn281Ile) c.817A>T n.839A>T | |
X | g.111401096T>C | CA414246026 | DCX | c.599A>G (p.Asn200Ser) c.842A>G (p.Asn281Ser) c.817A>G n.839A>G | |
X | g.111401096T>G | CA414246027 | DCX | c.599A>C (p.Asn200Thr) c.842A>C (p.Asn281Thr) c.817A>C n.839A>C | |
X | g.111401097T>A | CA414246028 | DCX | c.598A>T (p.Asn200Tyr) c.841A>T (p.Asn281Tyr) c.816A>T n.838A>T | ClinVar |
X | g.111401097T>C | CA414246029 | DCX | c.598A>G (p.Asn200Asp) c.841A>G (p.Asn281Asp) c.816A>G n.838A>G | |
X | g.111401097T>G | CA414246030 | DCX | c.598A>C (p.Asn200His) c.841A>C (p.Asn281His) c.816A>C n.838A>C | |
X | g.111401098C>A | CA518113984 | DCX | c.597G>T (p.Leu199=) c.840G>T (p.Leu280=) c.815G>T n.837G>T | |
X | g.111401098C>G | CA518113985 | DCX | c.597G>C (p.Leu199=) c.840G>C (p.Leu280=) c.815G>C n.837G>C | |
X | g.111401098C>T | CA518113986 | DCX | c.597G>A (p.Leu199=) c.840G>A (p.Leu280=) c.815G>A n.837G>A | |
X | g.111401099A= | CA2451697223 | DCX | c.596T= (p.Leu199=) c.839T= (p.Leu280=) c.814T= n.836T= | |
X | g.111401099A>C | CA414246032 | DCX | c.596T>G (p.Leu199Arg) c.839T>G (p.Leu280Arg) c.814T>G n.836T>G | ClinVar |
X | g.111401099A>G | CA172023 | DCX | c.596T>C (p.Leu199Pro) c.839T>C (p.Leu280Pro) c.814T>C n.836T>C | ClinVar dbSNP |
X | g.111401099A>T | CA414246031 | DCX | c.596T>A (p.Leu199Gln) c.839T>A (p.Leu280Gln) c.814T>A n.836T>A | |
X | g.111401100G>A | CA518113987 | DCX | c.595C>T (p.Leu199=) c.838C>T (p.Leu280=) c.813C>T n.835C>T | |
X | g.111401100G>C | CA414246033 | DCX | c.595C>G (p.Leu199Val) c.838C>G (p.Leu280Val) c.813C>G n.835C>G | |
X | g.111401100G>T | CA414246034 | DCX | c.595C>A (p.Leu199Met) c.838C>A (p.Leu280Met) c.813C>A n.835C>A | |
X | g.111401101A>C | CA518113988 | DCX | c.594T>G (p.Leu198=) c.837T>G (p.Leu279=) c.812T>G n.834T>G | |
X | g.111401101A>G | CA518113989 | DCX | c.594T>C (p.Leu198=) c.837T>C (p.Leu279=) c.812T>C n.834T>C | |
X | g.111401101A>T | CA518113990 | DCX | c.594T>A (p.Leu198=) c.837T>A (p.Leu279=) c.812T>A n.834T>A | |
X | g.111401102A>C | CA414246035 | DCX | c.593T>G (p.Leu198Arg) c.836T>G (p.Leu279Arg) c.811T>G n.833T>G | |
X | g.111401102A>G | CA414246036 | DCX | c.593T>C (p.Leu198Pro) c.836T>C (p.Leu279Pro) c.811T>C n.833T>C | |
X | g.111401102A>T | CA414246037 | DCX | c.593T>A (p.Leu198His) c.836T>A (p.Leu279His) c.811T>A n.833T>A | |
X | g.111401103G>A | CA414246038 | DCX | c.592C>T (p.Leu198Phe) c.835C>T (p.Leu279Phe) c.810C>T n.832C>T | |
X | g.111401103G>C | CA414246040 | DCX | c.592C>G (p.Leu198Val) c.835C>G (p.Leu279Val) c.810C>G n.832C>G | |
X | g.111401103G>T | CA414246039 | DCX | c.592C>A (p.Leu198Ile) c.835C>A (p.Leu279Ile) c.810C>A n.832C>A | |
X | g.111401104C>A | CA518113991 | DCX | c.591G>T (p.Val197=) c.834G>T (p.Val278=) c.809G>T n.831G>T | |
X | g.111401104C>G | CA518113992 | DCX | c.591G>C (p.Val197=) c.834G>C (p.Val278=) c.809G>C n.831G>C | |
X | g.111401104C>T | CA518113993 | DCX | c.591G>A (p.Val197=) c.834G>A (p.Val278=) c.809G>A n.831G>A | gnomAD v4 |
X | g.111401105A>C | CA414246041 | DCX | c.590T>G (p.Val197Gly) c.833T>G (p.Val278Gly) c.808T>G n.830T>G | |
X | g.111401105A>G | CA414246042 | DCX | c.590T>C (p.Val197Ala) c.833T>C (p.Val278Ala) c.808T>C n.830T>C | |
X | g.111401105A>T | CA414246043 | DCX | c.590T>A (p.Val197Glu) c.833T>A (p.Val278Glu) c.808T>A n.830T>A | |
X | g.111401106C>A | CA414246044 | DCX | c.589G>T (p.Val197Leu) c.832G>T (p.Val278Leu) c.807G>T n.829G>T | |
X | g.111401106C>G | CA414246045 | DCX | c.589G>C (p.Val197Leu) c.832G>C (p.Val278Leu) c.807G>C n.829G>C | |
X | g.111401106C>T | CA414246046 | DCX | c.589G>A (p.Val197Met) c.832G>A (p.Val278Met) c.807G>A n.829G>A | |
X | g.111401107A= | CA2451697224 | DCX | c.588T= (p.Arg196=) c.831T= (p.Arg277=) c.806T= n.828T= | |
X | g.111401107A>C | CA518113994 | DCX | c.588T>G (p.Arg196=) c.831T>G (p.Arg277=) c.806T>G n.828T>G | |
X | g.111401107A>G | CA172020 | DCX | c.588T>C (p.Arg196=) c.831T>C (p.Arg277=) c.806T>C n.828T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.111401107A>T | CA518113995 | DCX | c.588T>A (p.Arg196=) c.831T>A (p.Arg277=) c.806T>A n.828T>A | |
X | g.111401108C>A | CA414246047 | DCX | c.587G>T (p.Arg196Leu) c.830G>T (p.Arg277Leu) c.805G>T n.827G>T | ClinVar dbSNP |
X | g.111401108C= | CA2451697225 | DCX | c.587G= (p.Arg196=) c.830G= (p.Arg277=) c.805G= n.827G= | |
X | g.111401108C>G | CA414246048 | DCX | c.587G>C (p.Arg196Pro) c.830G>C (p.Arg277Pro) c.805G>C n.827G>C | |
X | g.111401108C>T | CA121606 | DCX | c.587G>A (p.Arg196His) c.830G>A (p.Arg277His) c.805G>A n.827G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.111401109G>A | CA172017 | DCX | c.586C>T (p.Arg196Cys) c.829C>T (p.Arg277Cys) c.804C>T n.826C>T | ClinVar dbSNP gnomAD v4 |
X | g.111401109G>C | CA172014 | DCX | c.586C>G (p.Arg196Gly) c.829C>G (p.Arg277Gly) c.804C>G n.826C>G | ClinVar dbSNP |
X | g.111401109G= | CA2451697227 | DCX | c.586C= (p.Arg196=) c.829C= (p.Arg277=) c.804C= n.826C= | |
X | g.111401109G>T | CA172011 | DCX | c.586C>A (p.Arg196Ser) c.829C>A (p.Arg277Ser) c.804C>A n.826C>A | ClinVar dbSNP |
X | g.111401109_111401117delinsGCACAGCCT | CA2451697226 | DCX | c.578_586delinsAGGCTGTGC (p.Lys193=) c.821_829delinsAGGCTGTGC (p.Lys274=) c.796_804delinsAGGCTGTGC n.818_826delinsAGGCTGTGC | |
X | g.111401110C>A | CA518113998 | DCX | c.585G>T (p.Val195=) c.828G>T (p.Val276=) c.803G>T n.825G>T | |
X | g.111401110C>G | CA518113997 | DCX | c.585G>C (p.Val195=) c.828G>C (p.Val276=) c.803G>C n.825G>C | |
X | g.111401110C>T | CA518113996 | DCX | c.585G>A (p.Val195=) c.828G>A (p.Val276=) c.803G>A n.825G>A | |
X | g.111401110_111401117del | CA172010 | DCX | c.578_585del (p.Lys193ThrfsTer13) c.821_828del (p.Lys274ThrfsTer13) c.796_803del n.818_825del | ClinVar dbSNP |
X | g.111401111A>C | CA414246049 | DCX | c.584T>G (p.Val195Gly) c.827T>G (p.Val276Gly) c.802T>G n.824T>G | |
X | g.111401111A>G | CA414246050 | DCX | c.584T>C (p.Val195Ala) c.827T>C (p.Val276Ala) c.802T>C n.824T>C | |
X | g.111401111A>T | CA414246051 | DCX | c.584T>A (p.Val195Glu) c.827T>A (p.Val276Glu) c.802T>A n.824T>A | |
X | g.111401112C>A | CA414246052 | DCX | c.583G>T (p.Val195Leu) c.826G>T (p.Val276Leu) c.801G>T n.823G>T | |
X | g.111401112C>G | CA414246053 | DCX | c.583G>C (p.Val195Leu) c.826G>C (p.Val276Leu) c.801G>C n.823G>C | |
X | g.111401112C>T | CA414246054 | DCX | c.583G>A (p.Val195Met) c.826G>A (p.Val276Met) c.801G>A n.823G>A | |
X | g.111401113A>C | CA518113999 | DCX | c.582T>G (p.Ala194=) c.825T>G (p.Ala275=) c.800T>G n.822T>G | |
X | g.111401113A>G | CA518114000 | DCX | c.582T>C (p.Ala194=) c.825T>C (p.Ala275=) c.800T>C n.822T>C | |
X | g.111401113A>T | CA518114001 | DCX | c.582T>A (p.Ala194=) c.825T>A (p.Ala275=) c.800T>A n.822T>A | |
X | g.111401114G>A | CA414246055 | DCX | c.581C>T (p.Ala194Val) c.824C>T (p.Ala275Val) c.799C>T n.821C>T | |
X | g.111401114G>C | CA414246056 | DCX | c.581C>G (p.Ala194Gly) c.824C>G (p.Ala275Gly) c.799C>G n.821C>G | |
X | g.111401114G>T | CA414246057 | DCX | c.581C>A (p.Ala194Asp) c.824C>A (p.Ala275Asp) c.799C>A n.821C>A | |
X | g.111401115C>A | CA414246058 | DCX | c.580G>T (p.Ala194Ser) c.823G>T (p.Ala275Ser) c.798G>T n.820G>T | |
X | g.111401115C>G | CA414246059 | DCX | c.580G>C (p.Ala194Pro) c.823G>C (p.Ala275Pro) c.798G>C n.820G>C | |
X | g.111401115C>T | CA414246060 | DCX | c.580G>A (p.Ala194Thr) c.823G>A (p.Ala275Thr) c.798G>A n.820G>A | |
X | g.111401116C>A | CA414246062 | DCX | c.579G>T (p.Lys193Asn) c.822G>T (p.Lys274Asn) c.797G>T n.819G>T | |
X | g.111401116C>G | CA414246061 | DCX | c.579G>C (p.Lys193Asn) c.822G>C (p.Lys274Asn) c.797G>C n.819G>C | |
X | g.111401116C>T | CA518114002 | DCX | c.579G>A (p.Lys193=) c.822G>A (p.Lys274=) c.797G>A n.819G>A | COSMIC COSMIC |
X | g.111401116_111401117delinsCT | CA2451697228 | DCX | c.578_579delinsAG (p.Lys193=) c.821_822delinsAG (p.Lys274=) c.796_797delinsAG n.818_819delinsAG | |
X | g.111401117T>A | CA414246063 | DCX | c.578A>T (p.Lys193Met) c.821A>T (p.Lys274Met) c.796A>T n.818A>T | |
X | g.111401117T>C | CA414246064 | DCX | c.578A>G (p.Lys193Arg) c.821A>G (p.Lys274Arg) c.796A>G n.818A>G | |
X | g.111401117T>G | CA414246065 | DCX | c.578A>C (p.Lys193Thr) c.821A>C (p.Lys274Thr) c.796A>C n.818A>C | |
X | g.111401118del | CA207795 | DCX | c.578del (p.Lys193ArgfsTer7) c.821del (p.Lys274ArgfsTer7) c.796del n.818del | ClinVar dbSNP |
X | g.111401118T>A | CA414246066 | DCX | c.577A>T (p.Lys193Ter) c.820A>T (p.Lys274Ter) c.795A>T n.817A>T | |
X | g.111401118T>C | CA414246067 | DCX | c.577A>G (p.Lys193Glu) c.820A>G (p.Lys274Glu) c.795A>G n.817A>G | |
X | g.111401118T>G | CA414246068 | DCX | c.577A>C (p.Lys193Gln) c.820A>C (p.Lys274Gln) c.795A>C n.817A>C | |
X | g.111401119C>A | CA518114003 | DCX | c.576G>T (p.Arg192=) c.819G>T (p.Arg273=) c.794G>T n.816G>T | |
X | g.111401119C>G | CA518114004 | DCX | c.576G>C (p.Arg192=) c.819G>C (p.Arg273=) c.794G>C n.816G>C | |
X | g.111401119C>T | CA518114005 | DCX | c.576G>A (p.Arg192=) c.819G>A (p.Arg273=) c.794G>A n.816G>A | |
X | g.111401120C>A | CA414246069 | DCX | c.575G>T (p.Arg192Leu) c.818G>T (p.Arg273Leu) c.793G>T n.815G>T | |
X | g.111401120C>G | CA414246070 | DCX | c.575G>C (p.Arg192Pro) c.818G>C (p.Arg273Pro) c.793G>C n.815G>C | |
X | g.111401120C>T | CA414246071 | DCX | c.575G>A (p.Arg192Gln) c.818G>A (p.Arg273Gln) c.793G>A n.815G>A | COSMIC COSMIC |
X | g.111401121G>A | CA121591 | DCX | c.574C>T (p.Arg192Trp) c.817C>T (p.Arg273Trp) c.792C>T n.814C>T | ClinVar dbSNP |
X | g.111401121G>C | CA414246072 | DCX | c.574C>G (p.Arg192Gly) c.817C>G (p.Arg273Gly) c.792C>G n.814C>G | |
X | g.111401121G= | CA2451697229 | DCX | c.574C= (p.Arg192=) c.817C= (p.Arg273=) c.792C= n.814C= | |
X | g.111401121G>T | CA518114006 | DCX | c.574C>A (p.Arg192=) c.817C>A (p.Arg273=) c.792C>A n.814C>A | dbSNP |
X | g.111401122A>C | CA518114007 | DCX | c.573T>G (p.Pro191=) c.816T>G (p.Pro272=) c.791T>G n.813T>G | |
X | g.111401122A>G | CA518114008 | DCX | c.573T>C (p.Pro191=) c.816T>C (p.Pro272=) c.791T>C n.813T>C | |
X | g.111401122A>T | CA518114009 | DCX | c.573T>A (p.Pro191=) c.816T>A (p.Pro272=) c.791T>A n.813T>A | |
X | g.111401123G>A | CA414246074 | DCX | c.572C>T (p.Pro191Leu) c.815C>T (p.Pro272Leu) c.790C>T n.812C>T | |
X | g.111401123G>C | CA172007 | DCX | c.572C>G (p.Pro191Arg) c.815C>G (p.Pro272Arg) c.790C>G n.812C>G | ClinVar dbSNP |
X | g.111401123G= | CA2451697230 | DCX | c.572C= (p.Pro191=) c.815C= (p.Pro272=) c.790C= n.812C= | |
X | g.111401123G>T | CA414246073 | DCX | c.572C>A (p.Pro191His) c.815C>A (p.Pro272His) c.790C>A n.812C>A | |
X | g.111401124G>A | CA414246075 | DCX | c.571C>T (p.Pro191Ser) c.814C>T (p.Pro272Ser) c.789C>T n.811C>T | |
X | g.111401124G>C | CA414246076 | DCX | c.571C>G (p.Pro191Ala) c.814C>G (p.Pro272Ala) c.789C>G n.811C>G | dbSNP gnomAD v2 gnomAD v4 |
X | g.111401124G= | CA2451697231 | DCX | c.571C= (p.Pro191=) c.814C= (p.Pro272=) c.789C= n.811C= | |
X | g.111401124G>T | CA172004 | DCX | c.571C>A (p.Pro191Thr) c.814C>A (p.Pro272Thr) c.789C>A n.811C>A | ClinVar dbSNP |
X | g.111401125C>A | CA414246077 | DCX | c.570G>T (p.Lys190Asn) c.813G>T (p.Lys271Asn) c.788G>T n.810G>T | |
X | g.111401125C= | CA2451697232 | DCX | c.570G= (p.Lys190=) c.813G= (p.Lys271=) c.788G= n.810G= | |
X | g.111401125C>G | CA414246078 | DCX | c.570G>C (p.Lys190Asn) c.813G>C (p.Lys271Asn) c.788G>C n.810G>C | |
X | g.111401125C>T | CA518114010 | DCX | c.570G>A (p.Lys190=) c.813G>A (p.Lys271=) c.788G>A n.810G>A | dbSNP gnomAD v3 gnomAD v4 |
X | g.111401126T>A | CA414246079 | DCX | c.569A>T (p.Lys190Met) c.812A>T (p.Lys271Met) c.787A>T n.809A>T | |
X | g.111401126T>C | CA414246081 | DCX | c.569A>G (p.Lys190Arg) c.812A>G (p.Lys271Arg) c.787A>G n.809A>G | |
X | g.111401126T>G | CA414246080 | DCX | c.569A>C (p.Lys190Thr) c.812A>C (p.Lys271Thr) c.787A>C n.809A>C | |
X | g.111401127T>A | CA414246082 | DCX | c.568A>T (p.Lys190Ter) c.811A>T (p.Lys271Ter) c.786A>T n.808A>T | |
X | g.111401127T>C | CA224222 | DCX | c.568A>G (p.Lys190Glu) c.811A>G (p.Lys271Glu) c.786A>G n.808A>G | ClinVar dbSNP |
X | g.111401127T>G | CA414246083 | DCX | c.568A>C (p.Lys190Gln) c.811A>C (p.Lys271Gln) c.786A>C n.808A>C | |
X | g.111401127T= | CA2451697233 | DCX | c.568A= (p.Lys190=) c.811A= (p.Lys271=) c.786A= n.808A= | |
X | g.111401127_111401131delinsGATGATGGTAA | CA2695235800 | DCX | c.564_568delinsTTACCATCATC (p.Val189_Lys190delinsTyrHisHisGln) c.807_811delinsTTACCATCATC (p.Val270_Lys271delinsTyrHisHisGln) c.782_786delinsTTACCATCATC n.804_808delinsTTACCATCATC | |
X | g.111401128C>A | CA518114011 | DCX | c.567G>T (p.Val189=) c.810G>T (p.Val270=) c.785G>T n.807G>T | |
X | g.111401128C= | CA2451697234 | DCX | c.567G= (p.Val189=) c.810G= (p.Val270=) c.785G= n.807G= | |
X | g.111401128C>G | CA518114012 | DCX | c.567G>C (p.Val189=) c.810G>C (p.Val270=) c.785G>C n.807G>C | |
X | g.111401128C>T | CA10493319 | DCX | c.567G>A (p.Val189=) c.810G>A (p.Val270=) c.785G>A n.807G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.111401129A>C | CA414246084 | DCX | c.566T>G (p.Val189Gly) c.809T>G (p.Val270Gly) c.784T>G n.806T>G | |
X | g.111401129A>G | CA414246085 | DCX | c.566T>C (p.Val189Ala) c.809T>C (p.Val270Ala) c.784T>C n.806T>C | |
X | g.111401129A>T | CA414246086 | DCX | c.566T>A (p.Val189Glu) c.809T>A (p.Val270Glu) c.784T>A n.806T>A | |
X | g.111401130C>A | CA414246087 | DCX | c.565G>T (p.Val189Leu) c.808G>T (p.Val270Leu) c.783G>T n.805G>T | |
X | g.111401130C>G | CA414246088 | DCX | c.565G>C (p.Val189Leu) c.808G>C (p.Val270Leu) c.783G>C n.805G>C | |
X | g.111401130C>T | CA414246089 | DCX | c.565G>A (p.Val189Met) c.808G>A (p.Val270Met) c.783G>A n.805G>A | gnomAD v4 |
X | g.111401131C>A | CA518114013 | DCX | c.564G>T (p.Gly188=) c.807G>T (p.Gly269=) c.782G>T n.804G>T | |
X | g.111401131C>G | CA518114014 | DCX | c.564G>C (p.Gly188=) c.807G>C (p.Gly269=) c.782G>C n.804G>C | |
X | g.111401131C>T | CA518114015 | DCX | c.564G>A (p.Gly188=) c.807G>A (p.Gly269=) c.782G>A n.804G>A | |
X | g.111401132C>A | CA414246090 | DCX | c.563G>T (p.Gly188Val) c.806G>T (p.Gly269Val) c.781G>T n.803G>T | |
X | g.111401132C>G | CA414246091 | DCX | c.563G>C (p.Gly188Ala) c.806G>C (p.Gly269Ala) c.781G>C n.803G>C | |
X | g.111401132C>T | CA414246092 | DCX | c.563G>A (p.Gly188Glu) c.806G>A (p.Gly269Glu) c.781G>A n.803G>A | |
X | g.111401133C>A | CA414246095 | DCX | c.562G>T (p.Gly188Trp) c.805G>T (p.Gly269Trp) c.780G>T n.802G>T | |
X | g.111401133C>G | CA414246094 | DCX | c.562G>C (p.Gly188Arg) c.805G>C (p.Gly269Arg) c.780G>C n.802G>C | |
X | g.111401133C>T | CA414246093 | DCX | c.562G>A (p.Gly188Arg) c.805G>A (p.Gly269Arg) c.780G>A n.802G>A | ClinVar dbSNP |
X | g.111401134A>C | CA414246096 | DCX | c.561T>G (p.Ser187Arg) c.804T>G (p.Ser268Arg) c.779T>G n.801T>G | |
X | g.111401134A>G | CA518114016 | DCX | c.561T>C (p.Ser187=) c.804T>C (p.Ser268=) c.779T>C n.801T>C | |
X | g.111401134A>T | CA414246097 | DCX | c.561T>A (p.Ser187Arg) c.804T>A (p.Ser268Arg) c.779T>A n.801T>A | |
X | g.111401135C>A | CA414246098 | DCX | c.560G>T (p.Ser187Ile) c.803G>T (p.Ser268Ile) c.778G>T n.800G>T | |
X | g.111401135C>G | CA414246099 | DCX | c.560G>C (p.Ser187Thr) c.803G>C (p.Ser268Thr) c.778G>C n.800G>C | |
X | g.111401135C>T | CA414246100 | DCX | c.560G>A (p.Ser187Asn) c.803G>A (p.Ser268Asn) c.778G>A n.800G>A | |
X | g.111401136T>A | CA414246101 | DCX | c.559A>T (p.Ser187Cys) c.802A>T (p.Ser268Cys) c.777A>T n.799A>T | |
X | g.111401136T>C | CA414246102 | DCX | c.559A>G (p.Ser187Gly) c.802A>G (p.Ser268Gly) c.777A>G n.799A>G | |
X | g.111401136T>G | CA414246103 | DCX | c.559A>C (p.Ser187Arg) c.802A>C (p.Ser268Arg) c.777A>C n.799A>C | gnomAD v4 |
X | g.111401137G>A | CA518114017 | DCX | c.558C>T (p.Arg186=) c.801C>T (p.Arg267=) c.776C>T n.798C>T | |
X | g.111401137G>C | CA518114018 | DCX | c.558C>G (p.Arg186=) c.801C>G (p.Arg267=) c.776C>G n.798C>G | |
X | g.111401137G>T | CA518114019 | DCX | c.558C>A (p.Arg186=) c.801C>A (p.Arg267=) c.776C>A n.798C>A | |
X | g.111401138C>A | CA171998 | DCX | c.557G>T (p.Arg186Leu) c.800G>T (p.Arg267Leu) c.775G>T n.797G>T | ClinVar dbSNP COSMIC COSMIC |
X | g.111401138C= | CA2451697235 | DCX | c.557G= (p.Arg186=) c.800G= (p.Arg267=) c.775G= n.797G= | |
X | g.111401138C>G | CA414246104 | DCX | c.557G>C (p.Arg186Pro) c.800G>C (p.Arg267Pro) c.775G>C n.797G>C | |
X | g.111401138C>T | CA171995 | DCX | c.557G>A (p.Arg186His) c.800G>A (p.Arg267His) c.775G>A n.797G>A | ClinVar dbSNP ExAC |
X | g.111401139G>A | CA171992 | DCX | c.556C>T (p.Arg186Cys) c.799C>T (p.Arg267Cys) c.774C>T n.796C>T | ClinVar dbSNP COSMIC COSMIC |
X | g.111401139G>C | CA414246106 | DCX | c.556C>G (p.Arg186Gly) c.799C>G (p.Arg267Gly) c.774C>G n.796C>G | |
X | g.111401139G= | CA2451697236 | DCX | c.556C= (p.Arg186=) c.799C= (p.Arg267=) c.774C= n.796C= | |
X | g.111401139G>T | CA414246105 | DCX | c.556C>A (p.Arg186Ser) c.799C>A (p.Arg267Ser) c.774C>A n.796C>A | |
X | g.111401139_111401142delinsGGAT | CA2451697237 | DCX | c.553_556delinsATCC (p.Ile185=) c.796_799delinsATCC (p.Ile266=) c.771_774delinsATCC n.793_796delinsATCC | |
X | g.111401140G>A | CA518114021 | DCX | c.555C>T (p.Ile185=) c.798C>T (p.Ile266=) c.773C>T n.795C>T | dbSNP gnomAD v2 gnomAD v4 |
X | g.111401140G>C | CA414246107 | DCX | c.555C>G (p.Ile185Met) c.798C>G (p.Ile266Met) c.773C>G n.795C>G | |
X | g.111401140G= | CA2451697239 | DCX | c.555C= (p.Ile185=) c.798C= (p.Ile266=) c.773C= n.795C= | |
X | g.111401140G>T | CA518114020 | DCX | c.555C>A (p.Ile185=) c.798C>A (p.Ile266=) c.773C>A n.795C>A | |
X | g.111401144_111401146del | CA2451697238 | DCX | c.553_555del (p.Ile185del) c.796_798del (p.Ile266del) c.771_773del n.793_795del | dbSNP |
X | g.111401141A>C | CA414246108 | DCX | c.554T>G (p.Ile185Ser) c.797T>G (p.Ile266Ser) c.772T>G n.794T>G | |
X | g.111401141A>G | CA414246109 | DCX | c.554T>C (p.Ile185Thr) c.797T>C (p.Ile266Thr) c.772T>C n.794T>C | |
X | g.111401141A>T | CA414246110 | DCX | c.554T>A (p.Ile185Asn) c.797T>A (p.Ile266Asn) c.772T>A n.794T>A | |
X | g.111401142T>A | CA414246111 | DCX | c.553A>T (p.Ile185Phe) c.796A>T (p.Ile266Phe) c.771A>T n.793A>T | |
X | g.111401142T>C | CA414246112 | DCX | c.553A>G (p.Ile185Val) c.796A>G (p.Ile266Val) c.771A>G n.793A>G | |
X | g.111401142T>G | CA414246113 | DCX | c.553A>C (p.Ile185Leu) c.796A>C (p.Ile266Leu) c.771A>C n.793A>C | |
X | g.111401143G>A | CA518114022 | DCX | c.552C>T (p.Ile184=) c.795C>T (p.Ile265=) c.770C>T n.792C>T | |
X | g.111401143G>C | CA414246114 | DCX | c.552C>G (p.Ile184Met) c.795C>G (p.Ile265Met) c.770C>G n.792C>G | |
X | g.111401143G>T | CA518114023 | DCX | c.552C>A (p.Ile184=) c.795C>A (p.Ile265=) c.770C>A n.792C>A | |
X | g.111401144A= | CA2451697240 | DCX | c.551T= (p.Ile184=) c.794T= (p.Ile265=) c.769T= n.791T= | |
X | g.111401144A>C | CA414246115 | DCX | c.551T>G (p.Ile184Ser) c.794T>G (p.Ile265Ser) c.769T>G n.791T>G | |
X | g.111401144A>G | CA414246116 | DCX | c.551T>C (p.Ile184Thr) c.794T>C (p.Ile265Thr) c.769T>C n.791T>C | |
X | g.111401144A>T | CA171989 | DCX | c.551T>A (p.Ile184Asn) c.794T>A (p.Ile265Asn) c.769T>A n.791T>A | ClinVar dbSNP |
X | g.111401145T>A | CA414246119 | DCX | c.550A>T (p.Ile184Phe) c.793A>T (p.Ile265Phe) c.768A>T n.790A>T | |
X | g.111401145T>C | CA414246118 | DCX | c.550A>G (p.Ile184Val) c.793A>G (p.Ile265Val) c.768A>G n.790A>G | dbSNP gnomAD v4 |
X | g.111401145T>G | CA414246117 | DCX | c.550A>C (p.Ile184Leu) c.793A>C (p.Ile265Leu) c.768A>C n.790A>C | |
X | g.111401145T= | CA2451697241 | DCX | c.550A= (p.Ile184=) c.793A= (p.Ile265=) c.768A= n.790A= | |
X | g.111401146G>A | CA518114024 | DCX | c.549C>T (p.Thr183=) c.792C>T (p.Thr264=) c.767C>T n.789C>T | |
X | g.111401146G>C | CA518114025 | DCX | c.549C>G (p.Thr183=) c.792C>G (p.Thr264=) c.767C>G n.789C>G | |
X | g.111401146G>T | CA518114026 | DCX | c.549C>A (p.Thr183=) c.792C>A (p.Thr264=) c.767C>A n.789C>A |