Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.44275389G>A | CA253383 | ALX4 | c.736C>T (p.Gln246Ter) c.214C>T (p.Gln72Ter) | ClinVar dbSNP |
11 | g.44275389G>C | CA380182214 | ALX4 | c.736C>G (p.Gln246Glu) c.214C>G (p.Gln72Glu) | |
11 | g.44275389G= | CA1967928932 | ALX4 | c.736C= (p.Gln246=) c.214C= (p.Gln72=) | |
11 | g.44275389G>T | CA380182215 | ALX4 | c.736C>A (p.Gln246Lys) c.214C>A (p.Gln72Lys) | |
11 | g.44275390T>A | CA380182216 | ALX4 | c.735A>T (p.Glu245Asp) c.213A>T (p.Glu71Asp) | |
11 | g.44275390T>C | CA473833877 | ALX4 | c.735A>G (p.Glu245=) c.213A>G (p.Glu71=) | |
11 | g.44275390T>G | CA380182217 | ALX4 | c.735A>C (p.Glu245Asp) c.213A>C (p.Glu71Asp) | |
11 | g.44275391T>A | CA380182218 | ALX4 | c.734A>T (p.Glu245Val) c.212A>T (p.Glu71Val) | |
11 | g.44275391T>C | CA380182219 | ALX4 | c.734A>G (p.Glu245Gly) c.212A>G (p.Glu71Gly) | |
11 | g.44275391T>G | CA380182220 | ALX4 | c.734A>C (p.Glu245Ala) c.212A>C (p.Glu71Ala) | |
11 | g.44275392C>A | CA380182221 | ALX4 | c.733G>T (p.Glu245Ter) c.211G>T (p.Glu71Ter) | |
11 | g.44275392C>G | CA380182222 | ALX4 | c.733G>C (p.Glu245Gln) c.211G>C (p.Glu71Gln) | |
11 | g.44275392C>T | CA380182223 | ALX4 | c.733G>A (p.Glu245Lys) c.211G>A (p.Glu71Lys) | |
11 | g.44275393C>A | CA473833878 | ALX4 | c.732G>T (p.Arg244=) c.210G>T (p.Arg70=) | |
11 | g.44275393C>G | CA473833879 | ALX4 | c.732G>C (p.Arg244=) c.210G>C (p.Arg70=) | |
11 | g.44275393C>T | CA473833880 | ALX4 | c.732G>A (p.Arg244=) c.210G>A (p.Arg70=) | |
11 | g.44275394C>A | CA380182226 | ALX4 | c.731G>T (p.Arg244Leu) c.209G>T (p.Arg70Leu) | |
11 | g.44275394C= | CA1967928936 | ALX4 | c.731G= (p.Arg244=) c.209G= (p.Arg70=) | |
11 | g.44275394C>G | CA380182225 | ALX4 | c.731G>C (p.Arg244Pro) c.209G>C (p.Arg70Pro) | |
11 | g.44275394C>T | CA380182224 | ALX4 | c.731G>A (p.Arg244Gln) c.209G>A (p.Arg70Gln) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.44275395G>A | CA380182227 | ALX4 | c.730C>T (p.Arg244Trp) c.208C>T (p.Arg70Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.44275395G>C | CA380182228 | ALX4 | c.730C>G (p.Arg244Gly) c.208C>G (p.Arg70Gly) | gnomAD v4 |
11 | g.44275395G= | CA1967928940 | ALX4 | c.730C= (p.Arg244=) c.208C= (p.Arg70=) | |
11 | g.44275395G>T | CA473833884 | ALX4 | c.730C>A (p.Arg244=) c.208C>A (p.Arg70=) | |
11 | g.44275396C>A | CA473833887 | ALX4 | c.729G>T (p.Ala243=) c.207G>T (p.Ala69=) | |
11 | g.44275396C= | CA1967928945 | ALX4 | c.729G= (p.Ala243=) c.207G= (p.Ala69=) | |
11 | g.44275396C>G | CA473833885 | ALX4 | c.729G>C (p.Ala243=) c.207G>C (p.Ala69=) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.44275396C>T | CA5955668 | ALX4 | c.729G>A (p.Ala243=) c.207G>A (p.Ala69=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.44275397G>A | CA5955669 | ALX4 | c.728C>T (p.Ala243Val) c.206C>T (p.Ala69Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.44275397G>C | CA380182229 | ALX4 | c.728C>G (p.Ala243Gly) c.206C>G (p.Ala69Gly) | |
11 | g.44275397G= | CA1967928952 | ALX4 | c.728C= (p.Ala243=) c.206C= (p.Ala69=) | |
11 | g.44275397G>T | CA380182230 | ALX4 | c.728C>A (p.Ala243Glu) c.206C>A (p.Ala69Glu) | dbSNP gnomAD v4 COSMIC |
11 | g.44275398C>A | CA380182231 | ALX4 | c.727G>T (p.Ala243Ser) c.205G>T (p.Ala69Ser) | |
11 | g.44275398C>G | CA380182232 | ALX4 | c.727G>C (p.Ala243Pro) c.205G>C (p.Ala69Pro) | |
11 | g.44275398C>T | CA380182233 | ALX4 | c.727G>A (p.Ala243Thr) c.205G>A (p.Ala69Thr) | |
11 | g.44275399A= | CA1967928956 | ALX4 | c.726T= (p.Tyr242=) c.204T= (p.Tyr68=) | |
11 | g.44275399A>C | CA380182234 | ALX4 | c.726T>G (p.Tyr242Ter) c.204T>G (p.Tyr68Ter) | |
11 | g.44275399A>G | CA473833888 | ALX4 | c.726T>C (p.Tyr242=) c.204T>C (p.Tyr68=) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.44275399A>T | CA380182235 | ALX4 | c.726T>A (p.Tyr242Ter) c.204T>A (p.Tyr68Ter) | |
11 | g.44275400T>A | CA380182238 | ALX4 | c.725A>T (p.Tyr242Phe) c.203A>T (p.Tyr68Phe) | |
11 | g.44275400T>C | CA380182237 | ALX4 | c.725A>G (p.Tyr242Cys) c.203A>G (p.Tyr68Cys) | |
11 | g.44275400T>G | CA380182236 | ALX4 | c.725A>C (p.Tyr242Ser) c.203A>C (p.Tyr68Ser) | |
11 | g.44275401A>C | CA380182239 | ALX4 | c.724T>G (p.Tyr242Asp) c.202T>G (p.Tyr68Asp) | |
11 | g.44275401A>G | CA380182240 | ALX4 | c.724T>C (p.Tyr242His) c.202T>C (p.Tyr68His) | gnomAD v4 |
11 | g.44275401A>T | CA380182241 | ALX4 | c.724T>A (p.Tyr242Asn) c.202T>A (p.Tyr68Asn) | |
11 | g.44275402C>A | CA473833890 | ALX4 | c.723G>T (p.Val241=) c.201G>T (p.Val67=) | |
11 | g.44275402C>G | CA473833891 | ALX4 | c.723G>C (p.Val241=) c.201G>C (p.Val67=) | |
11 | g.44275402C>T | CA473833892 | ALX4 | c.723G>A (p.Val241=) c.201G>A (p.Val67=) | |
11 | g.44275403A>C | CA380182242 | ALX4 | c.722T>G (p.Val241Gly) c.200T>G (p.Val67Gly) | |
11 | g.44275403A>G | CA380182243 | ALX4 | c.722T>C (p.Val241Ala) c.200T>C (p.Val67Ala) |