Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 | |
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 |