Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.111401228_111401231del | CA2561695268 | DCX | c.464_467del (p.Asn155ArgfsTer?) c.707_710del (p.Asn236ArgfsTer?) c.682_685del n.704_707del | |
X | g.111401231T>A | CA414246311 | DCX | c.464A>T (p.Asn155Ile) c.707A>T (p.Asn236Ile) c.682A>T n.704A>T | |
X | g.111401231T>C | CA414246313 | DCX | c.464A>G (p.Asn155Ser) c.707A>G (p.Asn236Ser) c.682A>G n.704A>G | dbSNP gnomAD v2 gnomAD v4 |
X | g.111401231T>G | CA414246312 | DCX | c.464A>C (p.Asn155Thr) c.707A>C (p.Asn236Thr) c.682A>C n.704A>C | |
X | g.111401231T= | CA2451697266 | DCX | c.464A= (p.Asn155=) c.707A= (p.Asn236=) c.682A= n.704A= | |
X | g.111401232del | CA2695235804 | DCX | c.464del (p.Asn155IlefsTer2) c.707del (p.Asn236IlefsTer2) c.682del n.704del | |
X | g.111401232T>A | CA414246314 | DCX | c.463A>T (p.Asn155Tyr) c.706A>T (p.Asn236Tyr) c.681A>T n.703A>T | |
X | g.111401232T>C | CA414246316 | DCX | c.463A>G (p.Asn155Asp) c.706A>G (p.Asn236Asp) c.681A>G n.703A>G | gnomAD v4 |
X | g.111401232T>G | CA414246315 | DCX | c.463A>C (p.Asn155His) c.706A>C (p.Asn236His) c.681A>C n.703A>C | |
X | g.111401233G>A | CA518114205 | DCX | c.462C>T (p.Ala154=) c.705C>T (p.Ala235=) c.680C>T n.702C>T | |
X | g.111401233G>C | CA518114206 | DCX | c.462C>G (p.Ala154=) c.705C>G (p.Ala235=) c.680C>G n.702C>G | |
X | g.111401233G>T | CA518114207 | DCX | c.462C>A (p.Ala154=) c.705C>A (p.Ala235=) c.680C>A n.702C>A | |
X | g.111401234G>A | CA414246317 | DCX | c.461C>T (p.Ala154Val) c.704C>T (p.Ala235Val) c.679C>T n.701C>T | |
X | g.111401234G>C | CA414246319 | DCX | c.461C>G (p.Ala154Gly) c.704C>G (p.Ala235Gly) c.679C>G n.701C>G | |
X | g.111401234G>T | CA414246318 | DCX | c.461C>A (p.Ala154Asp) c.704C>A (p.Ala235Asp) c.679C>A n.701C>A | |
X | g.111401234_111401235insTTAG | CA2509294496 | DCX | c.461_462insTAAC (p.Met156GlnfsTer10) c.704_705insTAAC (p.Met237GlnfsTer10) c.679_680insTAAC n.701_702insTAAC | |
X | g.111401235C>A | CA414246320 | DCX | c.460G>T (p.Ala154Ser) c.703G>T (p.Ala235Ser) c.678G>T n.700G>T | |
X | g.111401235C>G | CA414246321 | DCX | c.460G>C (p.Ala154Pro) c.703G>C (p.Ala235Pro) c.678G>C n.700G>C | |
X | g.111401235C>T | CA414246322 | DCX | c.460G>A (p.Ala154Thr) c.703G>A (p.Ala235Thr) c.678G>A n.700G>A | |
X | g.111401236A>C | CA518114208 | DCX | c.459T>G (p.Ser153=) c.702T>G (p.Ser234=) c.677T>G n.699T>G | |
X | g.111401236A>G | CA518114209 | DCX | c.459T>C (p.Ser153=) c.702T>C (p.Ser234=) c.677T>C n.699T>C | |
X | g.111401236A>T | CA518114210 | DCX | c.459T>A (p.Ser153=) c.702T>A (p.Ser234=) c.677T>A n.699T>A | |
X | g.111401237G>A | CA414246323 | DCX | c.458C>T (p.Ser153Phe) c.701C>T (p.Ser234Phe) c.676C>T n.698C>T | |
X | g.111401237G>C | CA414246324 | DCX | c.458C>G (p.Ser153Cys) c.701C>G (p.Ser234Cys) c.676C>G n.698C>G | |
X | g.111401237G>T | CA414246325 | DCX | c.458C>A (p.Ser153Tyr) c.701C>A (p.Ser234Tyr) c.676C>A n.698C>A | COSMIC COSMIC |
X | g.111401238A>C | CA414246326 | DCX | c.457T>G (p.Ser153Ala) c.700T>G (p.Ser234Ala) c.675T>G n.697T>G | |
X | g.111401238A>G | CA414246327 | DCX | c.457T>C (p.Ser153Pro) c.700T>C (p.Ser234Pro) c.675T>C n.697T>C | |
X | g.111401238A>T | CA414246328 | DCX | c.457T>A (p.Ser153Thr) c.700T>A (p.Ser234Thr) c.675T>A n.697T>A | |
X | g.111401239T>A | CA518114211 | DCX | c.456A>T (p.Thr152=) c.699A>T (p.Thr233=) c.674A>T n.696A>T | gnomAD v4 |
X | g.111401239T>C | CA518114212 | DCX | c.456A>G (p.Thr152=) c.699A>G (p.Thr233=) c.674A>G n.696A>G | gnomAD v4 |
X | g.111401239T>G | CA518114213 | DCX | c.456A>C (p.Thr152=) c.699A>C (p.Thr233=) c.674A>C n.696A>C | |
X | g.111401240G>A | CA414246331 | DCX | c.455C>T (p.Thr152Ile) c.698C>T (p.Thr233Ile) c.673C>T n.695C>T | |
X | g.111401240G>C | CA414246330 | DCX | c.455C>G (p.Thr152Arg) c.698C>G (p.Thr233Arg) c.673C>G n.695C>G | |
X | g.111401240G>T | CA414246329 | DCX | c.455C>A (p.Thr152Lys) c.698C>A (p.Thr233Lys) c.673C>A n.695C>A | |
X | g.111401241T>A | CA414246332 | DCX | c.454A>T (p.Thr152Ser) c.697A>T (p.Thr233Ser) c.672A>T n.694A>T | |
X | g.111401241T>C | CA414246333 | DCX | c.454A>G (p.Thr152Ala) c.697A>G (p.Thr233Ala) c.672A>G n.694A>G | gnomAD v4 |
X | g.111401241T>G | CA414246334 | DCX | c.454A>C (p.Thr152Pro) c.697A>C (p.Thr233Pro) c.672A>C n.694A>C | |
X | g.111401245dup | CA2695235805 | DCX | c.454dup (p.Thr152AsnfsTer13) c.697dup (p.Thr233AsnfsTer13) c.672dup n.694dup | |
X | g.111401245del | CA518114214 | DCX | c.454del (p.Thr152HisfsTer5) c.697del (p.Thr233HisfsTer5) c.672del n.694del | COSMIC |
X | g.111401242T>A | CA414246335 | DCX | c.453A>T (p.Lys151Asn) c.696A>T (p.Lys232Asn) c.671A>T n.693A>T | |
X | g.111401242T>C | CA518114215 | DCX | c.453A>G (p.Lys151=) c.696A>G (p.Lys232=) c.671A>G n.693A>G | |
X | g.111401242T>G | CA414246336 | DCX | c.453A>C (p.Lys151Asn) c.696A>C (p.Lys232Asn) c.671A>C n.693A>C | |
X | g.111401243T>A | CA414246337 | DCX | c.452A>T (p.Lys151Ile) c.695A>T (p.Lys232Ile) c.670A>T n.692A>T | |
X | g.111401243T>C | CA414246338 | DCX | c.452A>G (p.Lys151Arg) c.695A>G (p.Lys232Arg) c.670A>G n.692A>G | |
X | g.111401243T>G | CA414246339 | DCX | c.452A>C (p.Lys151Thr) c.695A>C (p.Lys232Thr) c.670A>C n.692A>C | |
X | g.111401244T>A | CA171966 | DCX | c.451A>T (p.Lys151Ter) c.694A>T (p.Lys232Ter) c.669A>T n.691A>T | ClinVar dbSNP |
X | g.111401244T>C | CA171963 | DCX | c.451A>G (p.Lys151Glu) c.694A>G (p.Lys232Glu) c.669A>G n.691A>G | ClinVar dbSNP |
X | g.111401244T>G | CA414246340 | DCX | c.451A>C (p.Lys151Gln) c.694A>C (p.Lys232Gln) c.669A>C n.691A>C | |
X | g.111401244T= | CA2451697267 | DCX | c.451A= (p.Lys151=) c.694A= (p.Lys232=) c.669A= n.691A= | |
X | g.111401245T>A | CA518114216 | DCX | c.450A>T (p.Val150=) c.693A>T (p.Val231=) c.668A>T n.690A>T |