UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.41610449G>A | CA8562979 | KRT16 | c.1162C>T (p.Gln388Ter) c.448C>T (p.Gln150Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610449G>C | CA399489767 | KRT16 | c.1162C>G (p.Gln388Glu) c.448C>G (p.Gln150Glu) | |
| 17 | g.41610449G= | CA2260098536 | KRT16 | c.1162C= (p.Gln388=) c.448C= (p.Gln150=) | |
| 17 | g.41610449G>T | CA399489768 | KRT16 | c.1162C>A (p.Gln388Lys) c.448C>A (p.Gln150Lys) | |
| 17 | g.41610450G>A | CA500205953 | KRT16 | c.1161C>T (p.Ala387=) c.447C>T (p.Ala149=) | dbSNP gnomAD v4 |
| 17 | g.41610450G>C | CA8562980 | KRT16 | c.1161C>G (p.Ala387=) c.447C>G (p.Ala149=) | dbSNP ExAC gnomAD v2 |
| 17 | g.41610450G= | CA2260098539 | KRT16 | c.1161C= (p.Ala387=) c.447C= (p.Ala149=) | |
| 17 | g.41610450G>T | CA500205952 | KRT16 | c.1161C>A (p.Ala387=) c.447C>A (p.Ala149=) | |
| 17 | g.41610451G>A | CA399489773 | KRT16 | c.1160C>T (p.Ala387Val) c.446C>T (p.Ala149Val) | |
| 17 | g.41610451G>C | CA399489772 | KRT16 | c.1160C>G (p.Ala387Gly) c.446C>G (p.Ala149Gly) | |
| 17 | g.41610451G>T | CA399489770 | KRT16 | c.1160C>A (p.Ala387Asp) c.446C>A (p.Ala149Asp) | |
| 17 | g.41610452C>A | CA399489774 | KRT16 | c.1159G>T (p.Ala387Ser) c.445G>T (p.Ala149Ser) | |
| 17 | g.41610452C>G | CA399489775 | KRT16 | c.1159G>C (p.Ala387Pro) c.445G>C (p.Ala149Pro) | |
| 17 | g.41610452C>T | CA399489777 | KRT16 | c.1159G>A (p.Ala387Thr) c.445G>A (p.Ala149Thr) | |
| 17 | g.41610453C>A | CA500205954 | KRT16 | c.1158G>T (p.Leu386=) c.444G>T (p.Leu148=) | |
| 17 | g.41610453C>G | CA500205955 | KRT16 | c.1158G>C (p.Leu386=) c.444G>C (p.Leu148=) | |
| 17 | g.41610453C>T | CA500205956 | KRT16 | c.1158G>A (p.Leu386=) c.444G>A (p.Leu148=) | |
| 17 | g.41610454A>C | CA399489779 | KRT16 | c.1157T>G (p.Leu386Arg) c.443T>G (p.Leu148Arg) | |
| 17 | g.41610454A>G | CA399489780 | KRT16 | c.1157T>C (p.Leu386Pro) c.443T>C (p.Leu148Pro) | |
| 17 | g.41610454A>T | CA399489782 | KRT16 | c.1157T>A (p.Leu386Gln) c.443T>A (p.Leu148Gln) | |
| 17 | g.41610455G>A | CA500205957 | KRT16 | c.1156C>T (p.Leu386=) c.442C>T (p.Leu148=) | |
| 17 | g.41610455G>C | CA399489784 | KRT16 | c.1156C>G (p.Leu386Val) c.442C>G (p.Leu148Val) | |
| 17 | g.41610455G>T | CA399489786 | KRT16 | c.1156C>A (p.Leu386Met) c.442C>A (p.Leu148Met) | |
| 17 | g.41610456C>A | CA399489788 | KRT16 | c.1155G>T (p.Gln385His) c.441G>T (p.Gln147His) | |
| 17 | g.41610456C>G | CA399489790 | KRT16 | c.1155G>C (p.Gln385His) c.441G>C (p.Gln147His) | gnomAD v4 |
| 17 | g.41610456C>T | CA500205958 | KRT16 | c.1155G>A (p.Gln385=) c.441G>A (p.Gln147=) | |
| 17 | g.41610457T>A | CA399489793 | KRT16 | c.1154A>T (p.Gln385Leu) c.440A>T (p.Gln147Leu) | |
| 17 | g.41610457T>C | CA399489794 | KRT16 | c.1154A>G (p.Gln385Arg) c.440A>G (p.Gln147Arg) | |
| 17 | g.41610457T>G | CA399489797 | KRT16 | c.1154A>C (p.Gln385Pro) c.440A>C (p.Gln147Pro) | |
| 17 | g.41610458G>A | CA399489801 | KRT16 | c.1153C>T (p.Gln385Ter) c.439C>T (p.Gln147Ter) | |
| 17 | g.41610458G>C | CA399489803 | KRT16 | c.1153C>G (p.Gln385Glu) c.439C>G (p.Gln147Glu) | |
| 17 | g.41610458G= | CA2260098542 | KRT16 | c.1153C= (p.Gln385=) c.439C= (p.Gln147=) | |
| 17 | g.41610458G>T | CA8562981 | KRT16 | c.1153C>A (p.Gln385Lys) c.439C>A (p.Gln147Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610459C>A | CA399489805 | KRT16 | c.1152G>T (p.Glu384Asp) c.438G>T (p.Glu146Asp) | |
| 17 | g.41610459C= | CA2260098544 | KRT16 | c.1152G= (p.Glu384=) c.438G= (p.Glu146=) | |
| 17 | g.41610459C>G | CA399489807 | KRT16 | c.1152G>C (p.Glu384Asp) c.438G>C (p.Glu146Asp) | |
| 17 | g.41610459C>T | CA290676072 | KRT16 | c.1152G>A (p.Glu384=) c.438G>A (p.Glu146=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610460T>A | CA399489810 | KRT16 | c.1151A>T (p.Glu384Val) c.437A>T (p.Glu146Val) | |
| 17 | g.41610460T>C | CA399489811 | KRT16 | c.1151A>G (p.Glu384Gly) c.437A>G (p.Glu146Gly) | |
| 17 | g.41610460T>G | CA399489813 | KRT16 | c.1151A>C (p.Glu384Ala) c.437A>C (p.Glu146Ala) | |
| 17 | g.41610461C>A | CA399489817 | KRT16 | c.1150G>T (p.Glu384Ter) c.436G>T (p.Glu146Ter) | COSMIC |
| 17 | g.41610461C= | CA2260098549 | KRT16 | c.1150G= (p.Glu384=) c.436G= (p.Glu146=) | |
| 17 | g.41610461C>G | CA399489815 | KRT16 | c.1150G>C (p.Glu384Gln) c.436G>C (p.Glu146Gln) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610461C>T | CA8562982 | KRT16 | c.1150G>A (p.Glu384Lys) c.436G>A (p.Glu146Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.41610462C>A | CA399489819 | KRT16 | c.1149G>T (p.Glu383Asp) c.435G>T (p.Glu145Asp) | |
| 17 | g.41610462C>G | CA399489821 | KRT16 | c.1149G>C (p.Glu383Asp) c.435G>C (p.Glu145Asp) | gnomAD v4 COSMIC |
| 17 | g.41610462C>T | CA500205959 | KRT16 | c.1149G>A (p.Glu383=) c.435G>A (p.Glu145=) | gnomAD v4 |
| 17 | g.41610463T>A | CA399489823 | KRT16 | c.1148A>T (p.Glu383Val) c.434A>T (p.Glu145Val) | |
| 17 | g.41610463T>C | CA399489824 | KRT16 | c.1148A>G (p.Glu383Gly) c.434A>G (p.Glu145Gly) | |
| 17 | g.41610463T>G | CA399489826 | KRT16 | c.1148A>C (p.Glu383Ala) c.434A>C (p.Glu145Ala) | |
| 17 | g.41610464C>A | CA8562983 | KRT16 | c.1147G>T (p.Glu383Ter) c.433G>T (p.Glu145Ter) | dbSNP ExAC gnomAD v2 |
| 17 | g.41610464C= | CA2260098551 | KRT16 | c.1147G= (p.Glu383=) c.433G= (p.Glu145=) | |
| 17 | g.41610464C>G | CA399489828 | KRT16 | c.1147G>C (p.Glu383Gln) c.433G>C (p.Glu145Gln) | gnomAD v4 |
| 17 | g.41610464C>T | CA399489829 | KRT16 | c.1147G>A (p.Glu383Lys) c.433G>A (p.Glu145Lys) | gnomAD v4 |
| 17 | g.41610465C>A | CA500205960 | KRT16 | c.1146G>T (p.Val382=) c.432G>T (p.Val144=) | gnomAD v4 |
| 17 | g.41610465C>G | CA500205961 | KRT16 | c.1146G>C (p.Val382=) c.432G>C (p.Val144=) | |
| 17 | g.41610465C>T | CA500205962 | KRT16 | c.1146G>A (p.Val382=) c.432G>A (p.Val144=) | |
| 17 | g.41610466A= | CA2260098554 | KRT16 | c.1145T= (p.Val382=) c.431T= (p.Val144=) | |
| 17 | g.41610466A>C | CA399489832 | KRT16 | c.1145T>G (p.Val382Gly) c.431T>G (p.Val144Gly) | |
| 17 | g.41610466A>G | CA399489833 | KRT16 | c.1145T>C (p.Val382Ala) c.431T>C (p.Val144Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41610466A>T | CA399489835 | KRT16 | c.1145T>A (p.Val382Glu) c.431T>A (p.Val144Glu) | |
| 17 | g.41610467C>A | CA399489838 | KRT16 | c.1144G>T (p.Val382Leu) c.430G>T (p.Val144Leu) | |
| 17 | g.41610467C>G | CA399489839 | KRT16 | c.1144G>C (p.Val382Leu) c.430G>C (p.Val144Leu) | |
| 17 | g.41610467C>T | CA399489840 | KRT16 | c.1144G>A (p.Val382Met) c.430G>A (p.Val144Met) | gnomAD v4 |
| 17 | g.41610468A>C | CA399489843 | KRT16 | c.1143T>G (p.Ser381Arg) c.429T>G (p.Ser143Arg) | |
| 17 | g.41610468A>G | CA500205963 | KRT16 | c.1143T>C (p.Ser381=) c.429T>C (p.Ser143=) | gnomAD v4 |
| 17 | g.41610468A>T | CA399489842 | KRT16 | c.1143T>A (p.Ser381Arg) c.429T>A (p.Ser143Arg) | |
| 17 | g.41610469C>A | CA399489844 | KRT16 | c.1142G>T (p.Ser381Ile) c.428G>T (p.Ser143Ile) | gnomAD v4 |
| 17 | g.41610469C>G | CA399489845 | KRT16 | c.1142G>C (p.Ser381Thr) c.428G>C (p.Ser143Thr) | |
| 17 | g.41610469C>T | CA399489846 | KRT16 | c.1142G>A (p.Ser381Asn) c.428G>A (p.Ser143Asn) | |
| 17 | g.41610470T>A | CA399489847 | KRT16 | c.1141A>T (p.Ser381Cys) c.427A>T (p.Ser143Cys) | |
| 17 | g.41610470T>C | CA399489848 | KRT16 | c.1141A>G (p.Ser381Gly) c.427A>G (p.Ser143Gly) | COSMIC |
| 17 | g.41610470T>G | CA399489850 | KRT16 | c.1141A>C (p.Ser381Arg) c.427A>C (p.Ser143Arg) | |
| 17 | g.41610471G>A | CA500205964 | KRT16 | c.1140C>T (p.Gly380=) c.426C>T (p.Gly142=) | gnomAD v4 |
| 17 | g.41610471G>C | CA500205966 | KRT16 | c.1140C>G (p.Gly380=) c.426C>G (p.Gly142=) | |
| 17 | g.41610471G>T | CA500205965 | KRT16 | c.1140C>A (p.Gly380=) c.426C>A (p.Gly142=) | |
| 17 | g.41610472C>A | CA399489851 | KRT16 | c.1139G>T (p.Gly380Val) c.425G>T (p.Gly142Val) | |
| 17 | g.41610472C>G | CA399489854 | KRT16 | c.1139G>C (p.Gly380Ala) c.425G>C (p.Gly142Ala) | |
| 17 | g.41610472C>T | CA399489852 | KRT16 | c.1139G>A (p.Gly380Asp) c.425G>A (p.Gly142Asp) | gnomAD v4 |
| 17 | g.41610473C>A | CA399489856 | KRT16 | c.1138G>T (p.Gly380Cys) c.424G>T (p.Gly142Cys) | |
| 17 | g.41610473C>G | CA399489858 | KRT16 | c.1138G>C (p.Gly380Arg) c.424G>C (p.Gly142Arg) | |
| 17 | g.41610473C>T | CA399489860 | KRT16 | c.1138G>A (p.Gly380Ser) c.424G>A (p.Gly142Ser) | |
| 17 | g.41610474A= | CA2260098558 | KRT16 | c.1137T= (p.Ile379=) c.423T= (p.Ile141=) | |
| 17 | g.41610474A>C | CA8562984 | KRT16 | c.1137T>G (p.Ile379Met) c.423T>G (p.Ile141Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.41610474A>G | CA500205967 | KRT16 | c.1137T>C (p.Ile379=) c.423T>C (p.Ile141=) | gnomAD v4 |
| 17 | g.41610474A>T | CA500205968 | KRT16 | c.1137T>A (p.Ile379=) c.423T>A (p.Ile141=) | |
| 17 | g.41610475A= | CA2260098560 | KRT16 | c.1136T= (p.Ile379=) c.422T= (p.Ile141=) | |
| 17 | g.41610475A>C | CA399489864 | KRT16 | c.1136T>G (p.Ile379Ser) c.422T>G (p.Ile141Ser) | |
| 17 | g.41610475A>G | CA8562985 | KRT16 | c.1136T>C (p.Ile379Thr) c.422T>C (p.Ile141Thr) | dbSNP ExAC gnomAD v2 |
| 17 | g.41610475A>T | CA399489865 | KRT16 | c.1136T>A (p.Ile379Asn) c.422T>A (p.Ile141Asn) | |
| 17 | g.41610476T>A | CA399489867 | KRT16 | c.1135A>T (p.Ile379Phe) c.421A>T (p.Ile141Phe) | |
| 17 | g.41610476T>C | CA399489869 | KRT16 | c.1135A>G (p.Ile379Val) c.421A>G (p.Ile141Val) | |
| 17 | g.41610476T>G | CA399489871 | KRT16 | c.1135A>C (p.Ile379Leu) c.421A>C (p.Ile141Leu) | |
| 17 | g.41610477C>A | CA500205969 | KRT16 | c.1134G>T (p.Leu378=) c.420G>T (p.Leu140=) | |
| 17 | g.41610477C>G | CA500205970 | KRT16 | c.1134G>C (p.Leu378=) c.420G>C (p.Leu140=) | |
| 17 | g.41610477C>T | CA500205971 | KRT16 | c.1134G>A (p.Leu378=) c.420G>A (p.Leu140=) | |
| 17 | g.41610478A>C | CA399489872 | KRT16 | c.1133T>G (p.Leu378Arg) c.419T>G (p.Leu140Arg) | |
| 17 | g.41610478A>G | CA399489874 | KRT16 | c.1133T>C (p.Leu378Pro) c.419T>C (p.Leu140Pro) | |
| 17 | g.41610478A>T | CA399489876 | KRT16 | c.1133T>A (p.Leu378Gln) c.419T>A (p.Leu140Gln) | |
| 17 | g.41610478_41610479delinsAG | CA2260098562 | KRT16 | c.1132_1133delinsCT (p.Leu378=) c.418_419delinsCT (p.Leu140=) | |
| 17 | g.41610479del | CA8562986 | KRT16 | c.1132del (p.Leu378Ter) c.418del (p.Leu140Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.41610479G>A | CA500205972 | KRT16 | c.1132C>T (p.Leu378=) c.418C>T (p.Leu140=) | |
| 17 | g.41610479G>C | CA399489881 | KRT16 | c.1132C>G (p.Leu378Val) c.418C>G (p.Leu140Val) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610479G= | CA2260098565 | KRT16 | c.1132C= (p.Leu378=) c.418C= (p.Leu140=) | |
| 17 | g.41610479G>T | CA399489878 | KRT16 | c.1132C>A (p.Leu378Met) c.418C>A (p.Leu140Met) | gnomAD v4 |
| 17 | g.41610480T>A | CA500205973 | KRT16 | c.1131A>T (p.Gly377=) c.417A>T (p.Gly139=) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610480T>C | CA500205974 | KRT16 | c.1131A>G (p.Gly377=) c.417A>G (p.Gly139=) | |
| 17 | g.41610480T>G | CA500205975 | KRT16 | c.1131A>C (p.Gly377=) c.417A>C (p.Gly139=) | |
| 17 | g.41610480T= | CA2260098569 | KRT16 | c.1131A= (p.Gly377=) c.417A= (p.Gly139=) | |
| 17 | g.41610482_41610489del | CA2576267843 | KRT16 | c.1124_1131del (p.Ile375ThrfsTer15) c.410_417del (p.Ile137ThrfsTer15) | |
| 17 | g.41610481C>A | CA399489882 | KRT16 | c.1130G>T (p.Gly377Val) c.416G>T (p.Gly139Val) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41610481C= | CA2260098571 | KRT16 | c.1130G= (p.Gly377=) c.416G= (p.Gly139=) | |
| 17 | g.41610481C>G | CA399489884 | KRT16 | c.1130G>C (p.Gly377Ala) c.416G>C (p.Gly139Ala) | dbSNP |
| 17 | g.41610481C>T | CA399489885 | KRT16 | c.1130G>A (p.Gly377Glu) c.416G>A (p.Gly139Glu) | |
| 17 | g.41610481_41610482insT | CA8562987 | KRT16 | c.1129_1130insA (p.Gly377GlufsTer16) c.415_416insA (p.Gly139GlufsTer16) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.41610482C>A | CA399489888 | KRT16 | c.1129G>T (p.Gly377Ter) c.415G>T (p.Gly139Ter) | |
| 17 | g.41610482C= | CA2260098749 | KRT16 | c.1129G= (p.Gly377=) c.415G= (p.Gly139=) | |
| 17 | g.41610482C>G | CA399489890 | KRT16 | c.1129G>C (p.Gly377Arg) c.415G>C (p.Gly139Arg) | |
| 17 | g.41610482C>T | CA8562988 | KRT16 | c.1129G>A (p.Gly377Arg) c.415G>A (p.Gly139Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.41610483C>A | CA399489892 | KRT16 | c.1128G>T (p.Gln376His) c.414G>T (p.Gln138His) | |
| 17 | g.41610483C>G | CA399489894 | KRT16 | c.1128G>C (p.Gln376His) c.414G>C (p.Gln138His) | |
| 17 | g.41610483C>T | CA500205976 | KRT16 | c.1128G>A (p.Gln376=) c.414G>A (p.Gln138=) | |
| 17 | g.41610484T>A | CA399489896 | KRT16 | c.1127A>T (p.Gln376Leu) c.413A>T (p.Gln138Leu) | |
| 17 | g.41610484T>C | CA399489897 | KRT16 | c.1127A>G (p.Gln376Arg) c.413A>G (p.Gln138Arg) | |
| 17 | g.41610484T>G | CA399489899 | KRT16 | c.1127A>C (p.Gln376Pro) c.413A>C (p.Gln138Pro) | |
| 17 | g.41610485G>A | CA399489900 | KRT16 | c.1126C>T (p.Gln376Ter) c.412C>T (p.Gln138Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41610485G>C | CA399489902 | KRT16 | c.1126C>G (p.Gln376Glu) c.412C>G (p.Gln138Glu) | |
| 17 | g.41610485G= | CA2260098750 | KRT16 | c.1126C= (p.Gln376=) c.412C= (p.Gln138=) | |
| 17 | g.41610485G>T | CA399489901 | KRT16 | c.1126C>A (p.Gln376Lys) c.412C>A (p.Gln138Lys) | gnomAD v4 |
| 17 | g.41610486G>A | CA500205977 | KRT16 | c.1125C>T (p.Ile375=) c.411C>T (p.Ile137=) | |
| 17 | g.41610486G>C | CA399489904 | KRT16 | c.1125C>G (p.Ile375Met) c.411C>G (p.Ile137Met) | |
| 17 | g.41610486G= | CA2260098751 | KRT16 | c.1125C= (p.Ile375=) c.411C= (p.Ile137=) | |
| 17 | g.41610486G>T | CA500205978 | KRT16 | c.1125C>A (p.Ile375=) c.411C>A (p.Ile137=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 17 | g.41610487A>C | CA399489910 | KRT16 | c.1124T>G (p.Ile375Ser) c.410T>G (p.Ile137Ser) | |
| 17 | g.41610487A>G | CA399489906 | KRT16 | c.1124T>C (p.Ile375Thr) c.410T>C (p.Ile137Thr) | |
| 17 | g.41610487A>T | CA399489908 | KRT16 | c.1124T>A (p.Ile375Asn) c.410T>A (p.Ile137Asn) | |
| 17 | g.41610488T>A | CA399489912 | KRT16 | c.1123A>T (p.Ile375Phe) c.409A>T (p.Ile137Phe) | |
| 17 | g.41610488T>C | CA399489913 | KRT16 | c.1123A>G (p.Ile375Val) c.409A>G (p.Ile137Val) | gnomAD v4 |
| 17 | g.41610488T>G | CA399489914 | KRT16 | c.1123A>C (p.Ile375Leu) c.409A>C (p.Ile137Leu) | |
| 17 | g.41610489C>A | CA399489916 | KRT16 | c.1122G>T (p.Gln374His) c.408G>T (p.Gln136His) | |
| 17 | g.41610489C>G | CA399489918 | KRT16 | c.1122G>C (p.Gln374His) c.408G>C (p.Gln136His) | |
| 17 | g.41610489C>T | CA500205979 | KRT16 | c.1122G>A (p.Gln374=) c.408G>A (p.Gln136=) | |
| 17 | g.41610490T>A | CA399489920 | KRT16 | c.1121A>T (p.Gln374Leu) c.407A>T (p.Gln136Leu) | |
| 17 | g.41610490T>C | CA399489922 | KRT16 | c.1121A>G (p.Gln374Arg) c.407A>G (p.Gln136Arg) | |
| 17 | g.41610490T>G | CA399489924 | KRT16 | c.1121A>C (p.Gln374Pro) c.407A>C (p.Gln136Pro) | |
| 17 | g.41610491G>A | CA399489926 | KRT16 | c.1120C>T (p.Gln374Ter) c.406C>T (p.Gln136Ter) | |
| 17 | g.41610491G>C | CA399489927 | KRT16 | c.1120C>G (p.Gln374Glu) c.406C>G (p.Gln136Glu) | |
| 17 | g.41610491G>T | CA399489928 | KRT16 | c.1120C>A (p.Gln374Lys) c.406C>A (p.Gln136Lys) | |
| 17 | g.41610492G>A | CA500205982 | KRT16 | c.1119C>T (p.Ser373=) c.405C>T (p.Ser135=) | dbSNP gnomAD v4 |
| 17 | g.41610492G>C | CA500205980 | KRT16 | c.1119C>G (p.Ser373=) c.405C>G (p.Ser135=) | |
| 17 | g.41610492G= | CA2260098752 | KRT16 | c.1119C= (p.Ser373=) c.405C= (p.Ser135=) | |
| 17 | g.41610492G>T | CA500205981 | KRT16 | c.1119C>A (p.Ser373=) c.405C>A (p.Ser135=) | |
| 17 | g.41610493G>A | CA399489930 | KRT16 | c.1118C>T (p.Ser373Phe) c.404C>T (p.Ser135Phe) | |
| 17 | g.41610493G>C | CA399489932 | KRT16 | c.1118C>G (p.Ser373Cys) c.404C>G (p.Ser135Cys) | |
| 17 | g.41610493G= | CA2260098753 | KRT16 | c.1118C= (p.Ser373=) c.404C= (p.Ser135=) | |
| 17 | g.41610493G>T | CA399489931 | KRT16 | c.1118C>A (p.Ser373Tyr) c.404C>A (p.Ser135Tyr) | dbSNP gnomAD v2 |
| 17 | g.41610494del | CA2637835964 | KRT16 | c.1117del (p.Ser373ProfsTer6) c.403del (p.Ser135ProfsTer6) | gnomAD v4 |
| 17 | g.41610494A= | CA2260098754 | KRT16 | c.1117T= (p.Ser373=) c.403T= (p.Ser135=) | |
| 17 | g.41610494A>C | CA399489934 | KRT16 | c.1117T>G (p.Ser373Ala) c.403T>G (p.Ser135Ala) | ClinVar dbSNP gnomAD v4 |
| 17 | g.41610494A>G | CA399489936 | KRT16 | c.1117T>C (p.Ser373Pro) c.403T>C (p.Ser135Pro) | |
| 17 | g.41610494A>T | CA399489938 | KRT16 | c.1117T>A (p.Ser373Thr) c.403T>A (p.Ser135Thr) | |
| 17 | g.41610495C>A | CA500205983 | KRT16 | c.1116G>T (p.Leu372=) c.402G>T (p.Leu134=) | |
| 17 | g.41610495C= | CA2260098755 | KRT16 | c.1116G= (p.Leu372=) c.402G= (p.Leu134=) | |
| 17 | g.41610495C>G | CA500205984 | KRT16 | c.1116G>C (p.Leu372=) c.402G>C (p.Leu134=) | |
| 17 | g.41610495C>T | CA500205985 | KRT16 | c.1116G>A (p.Leu372=) c.402G>A (p.Leu134=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.41610496A>C | CA399489939 | KRT16 | c.1115T>G (p.Leu372Arg) c.401T>G (p.Leu134Arg) | |
| 17 | g.41610496A>G | CA399489941 | KRT16 | c.1115T>C (p.Leu372Pro) c.401T>C (p.Leu134Pro) | |
| 17 | g.41610496A>T | CA399489943 | KRT16 | c.1115T>A (p.Leu372Gln) c.401T>A (p.Leu134Gln) | |
| 17 | g.41610497G>A | CA500205986 | KRT16 | c.1114C>T (p.Leu372=) c.400C>T (p.Leu134=) | gnomAD v4 |
| 17 | g.41610497G>C | CA399489944 | KRT16 | c.1114C>G (p.Leu372Val) c.400C>G (p.Leu134Val) | |
| 17 | g.41610497G>T | CA399489945 | KRT16 | c.1114C>A (p.Leu372Met) c.400C>A (p.Leu134Met) | |
| 17 | g.41610497_41610498delinsGC | CA2260098756 | KRT16 | c.1113_1114delinsGC (p.Gln371=) c.399_400delinsGC (p.Gln133=) | |
| 17 | g.41610498del | CA2260098757 | KRT16 | c.1113del (p.Gln371HisfsTer8) c.399del (p.Gln133HisfsTer8) | dbSNP gnomAD v4 |
| 17 | g.41610498C>A | CA399489946 | KRT16 | c.1113G>T (p.Gln371His) c.399G>T (p.Gln133His) | |
| 17 | g.41610498C>G | CA399489948 | KRT16 | c.1113G>C (p.Gln371His) c.399G>C (p.Gln133His) | |
| 17 | g.41610498C>T | CA500205987 | KRT16 | c.1113G>A (p.Gln371=) c.399G>A (p.Gln133=) | |
| 17 | g.41610499T>A | CA399489951 | KRT16 | c.1112A>T (p.Gln371Leu) c.398A>T (p.Gln133Leu) | |
| 17 | g.41610499T>C | CA399489954 | KRT16 | c.1112A>G (p.Gln371Arg) c.398A>G (p.Gln133Arg) | |
| 17 | g.41610499T>G | CA399489949 | KRT16 | c.1112A>C (p.Gln371Pro) c.398A>C (p.Gln133Pro) | |
| 17 | g.41610500G>A | CA8562989 | KRT16 | c.1111C>T (p.Gln371Ter) c.397C>T (p.Gln133Ter) | dbSNP ExAC gnomAD v2 |
| 17 | g.41610500G>C | CA399489956 | KRT16 | c.1111C>G (p.Gln371Glu) c.397C>G (p.Gln133Glu) | |
| 17 | g.41610500G= | CA2260098758 | KRT16 | c.1111C= (p.Gln371=) c.397C= (p.Gln133=) | |
| 17 | g.41610500G>T | CA399489958 | KRT16 | c.1111C>A (p.Gln371Lys) c.397C>A (p.Gln133Lys) | |
| 17 | g.41610501C>A | CA399489960 | KRT16 | c.1110G>T (p.Met370Ile) c.396G>T (p.Met132Ile) | |
| 17 | g.41610501C= | CA2260098759 | KRT16 | c.1110G= (p.Met370=) c.396G= (p.Met132=) | |
| 17 | g.41610501C>G | CA399489962 | KRT16 | c.1110G>C (p.Met370Ile) c.396G>C (p.Met132Ile) | |
| 17 | g.41610501C>T | CA399489964 | KRT16 | c.1110G>A (p.Met370Ile) c.396G>A (p.Met132Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41610501_41610502delinsCA | CA2260098760 | KRT16 | c.1109_1110delinsTG (p.Met370=) c.395_396delinsTG (p.Met132=) | |
| 17 | g.41610502del | CA983759045 | KRT16 | c.1109del (p.Met370SerfsTer9) c.395del (p.Met132SerfsTer9) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610502A>C | CA399489968 | KRT16 | c.1109T>G (p.Met370Arg) c.395T>G (p.Met132Arg) | |
| 17 | g.41610502A>G | CA399489965 | KRT16 | c.1109T>C (p.Met370Thr) c.395T>C (p.Met132Thr) | |
| 17 | g.41610502A>T | CA399489967 | KRT16 | c.1109T>A (p.Met370Lys) c.395T>A (p.Met132Lys) | |
| 17 | g.41610503T>A | CA399489969 | KRT16 | c.1108A>T (p.Met370Leu) c.394A>T (p.Met132Leu) | COSMIC |
| 17 | g.41610503T>C | CA8562990 | KRT16 | c.1108A>G (p.Met370Val) c.394A>G (p.Met132Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610503T>G | CA399489972 | KRT16 | c.1108A>C (p.Met370Leu) c.394A>C (p.Met132Leu) | |
| 17 | g.41610503T= | CA2260098761 | KRT16 | c.1108A= (p.Met370=) c.394A= (p.Met132=) | |
| 17 | g.41610504G>A | CA500205988 | KRT16 | c.1107C>T (p.Cys369=) c.393C>T (p.Cys131=) | |
| 17 | g.41610504G>C | CA399489974 | KRT16 | c.1107C>G (p.Cys369Trp) c.393C>G (p.Cys131Trp) | |
| 17 | g.41610504G= | CA2260098762 | KRT16 | c.1107C= (p.Cys369=) c.393C= (p.Cys131=) | |
| 17 | g.41610504G>T | CA399489975 | KRT16 | c.1107C>A (p.Cys369Ter) c.393C>A (p.Cys131Ter) | dbSNP |
| 17 | g.41610505C>A | CA399489978 | KRT16 | c.1106G>T (p.Cys369Phe) c.392G>T (p.Cys131Phe) | |
| 17 | g.41610505C>G | CA399489981 | KRT16 | c.1106G>C (p.Cys369Ser) c.392G>C (p.Cys131Ser) | |
| 17 | g.41610505C>T | CA399489980 | KRT16 | c.1106G>A (p.Cys369Tyr) c.392G>A (p.Cys131Tyr) | |
| 17 | g.41610506A= | CA2260098763 | KRT16 | c.1105T= (p.Cys369=) c.391T= (p.Cys131=) | |
| 17 | g.41610506A>C | CA399489982 | KRT16 | c.1105T>G (p.Cys369Gly) c.391T>G (p.Cys131Gly) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610506A>G | CA399489984 | KRT16 | c.1105T>C (p.Cys369Arg) c.391T>C (p.Cys131Arg) | |
| 17 | g.41610506A>T | CA399489986 | KRT16 | c.1105T>A (p.Cys369Ser) c.391T>A (p.Cys131Ser) | |
| 17 | g.41610507G>A | CA290676115 | KRT16 | c.1104C>T (p.Tyr368=) c.390C>T (p.Tyr130=) | dbSNP gnomAD v4 |
| 17 | g.41610507G>C | CA399489990 | KRT16 | c.1104C>G (p.Tyr368Ter) c.390C>G (p.Tyr130Ter) | gnomAD v4 |
| 17 | g.41610507G= | CA2260098764 | KRT16 | c.1104C= (p.Tyr368=) c.390C= (p.Tyr130=) | |
| 17 | g.41610507G>T | CA399489992 | KRT16 | c.1104C>A (p.Tyr368Ter) c.390C>A (p.Tyr130Ter) | |
| 17 | g.41610508T>A | CA399489994 | KRT16 | c.1103A>T (p.Tyr368Phe) c.389A>T (p.Tyr130Phe) | |
| 17 | g.41610508T>C | CA399489995 | KRT16 | c.1103A>G (p.Tyr368Cys) c.389A>G (p.Tyr130Cys) | |
| 17 | g.41610508T>G | CA399489997 | KRT16 | c.1103A>C (p.Tyr368Ser) c.389A>C (p.Tyr130Ser) | gnomAD v4 |
| 17 | g.41610509A= | CA2260098765 | KRT16 | c.1102T= (p.Tyr368=) c.388T= (p.Tyr130=) | |
| 17 | g.41610509A>C | CA399489999 | KRT16 | c.1102T>G (p.Tyr368Asp) c.388T>G (p.Tyr130Asp) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610509A>G | CA399490001 | KRT16 | c.1102T>C (p.Tyr368His) c.388T>C (p.Tyr130His) | |
| 17 | g.41610509A>T | CA399490003 | KRT16 | c.1102T>A (p.Tyr368Asn) c.388T>A (p.Tyr130Asn) | |
| 17 | g.41610510G>A | CA500205989 | KRT16 | c.1101C>T (p.Arg367=) c.387C>T (p.Arg129=) | |
| 17 | g.41610510G>C | CA500205990 | KRT16 | c.1101C>G (p.Arg367=) c.387C>G (p.Arg129=) | gnomAD v4 |
| 17 | g.41610510G>T | CA500205991 | KRT16 | c.1101C>A (p.Arg367=) c.387C>A (p.Arg129=) | |
| 17 | g.41610511C>A | CA399490006 | KRT16 | c.1100G>T (p.Arg367Leu) c.386G>T (p.Arg129Leu) | |
| 17 | g.41610511C= | CA2260098766 | KRT16 | c.1100G= (p.Arg367=) c.386G= (p.Arg129=) | |
| 17 | g.41610511C>G | CA399490008 | KRT16 | c.1100G>C (p.Arg367Pro) c.386G>C (p.Arg129Pro) | |
| 17 | g.41610511C>T | CA399490004 | KRT16 | c.1100G>A (p.Arg367His) c.386G>A (p.Arg129His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610512G>A | CA8562991 | KRT16 | c.1099C>T (p.Arg367Cys) c.385C>T (p.Arg129Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.41610512G>C | CA399490010 | KRT16 | c.1099C>G (p.Arg367Gly) c.385C>G (p.Arg129Gly) | |
| 17 | g.41610512G= | CA2260098767 | KRT16 | c.1099C= (p.Arg367=) c.385C= (p.Arg129=) | |
| 17 | g.41610512G>T | CA399490012 | KRT16 | c.1099C>A (p.Arg367Ser) c.385C>A (p.Arg129Ser) | |
| 17 | g.41610513G>A | CA500205992 | KRT16 | c.1098C>T (p.Gly366=) c.384C>T (p.Gly128=) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610513G>C | CA500205994 | KRT16 | c.1098C>G (p.Gly366=) c.384C>G (p.Gly128=) | |
| 17 | g.41610513G= | CA2260098768 | KRT16 | c.1098C= (p.Gly366=) c.384C= (p.Gly128=) | |
| 17 | g.41610513G>T | CA500205993 | KRT16 | c.1098C>A (p.Gly366=) c.384C>A (p.Gly128=) | |
| 17 | g.41610514C>A | CA399490014 | KRT16 | c.1097G>T (p.Gly366Val) c.383G>T (p.Gly128Val) | |
| 17 | g.41610514C= | CA2260098769 | KRT16 | c.1097G= (p.Gly366=) c.383G= (p.Gly128=) | |
| 17 | g.41610514C>G | CA399490018 | KRT16 | c.1097G>C (p.Gly366Ala) c.383G>C (p.Gly128Ala) | |
| 17 | g.41610514C>T | CA8562992 | KRT16 | c.1097G>A (p.Gly366Asp) c.383G>A (p.Gly128Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610515C>A | CA8562993 | KRT16 | c.1096G>T (p.Gly366Cys) c.382G>T (p.Gly128Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610515C= | CA2260098770 | KRT16 | c.1096G= (p.Gly366=) c.382G= (p.Gly128=) | |
| 17 | g.41610515C>G | CA399490022 | KRT16 | c.1096G>C (p.Gly366Arg) c.382G>C (p.Gly128Arg) | |
| 17 | g.41610515C>T | CA290676152 | KRT16 | c.1096G>A (p.Gly366Ser) c.382G>A (p.Gly128Ser) | dbSNP |
| 17 | g.41610516T>A | CA399490025 | KRT16 | c.1095A>T (p.Lys365Asn) c.381A>T (p.Lys127Asn) | |
| 17 | g.41610516T>C | CA500205995 | KRT16 | c.1095A>G (p.Lys365=) c.381A>G (p.Lys127=) | |
| 17 | g.41610516T>G | CA399490026 | KRT16 | c.1095A>C (p.Lys365Asn) c.381A>C (p.Lys127Asn) | gnomAD v4 |
| 17 | g.41610517T>A | CA399490031 | KRT16 | c.1094A>T (p.Lys365Ile) c.380A>T (p.Lys127Ile) | |
| 17 | g.41610517T>C | CA399490029 | KRT16 | c.1094A>G (p.Lys365Arg) c.380A>G (p.Lys127Arg) | gnomAD v4 |
| 17 | g.41610517T>G | CA399490028 | KRT16 | c.1094A>C (p.Lys365Thr) c.380A>C (p.Lys127Thr) | |
| 17 | g.41610518T>A | CA399490033 | KRT16 | c.1093A>T (p.Lys365Ter) c.379A>T (p.Lys127Ter) | |
| 17 | g.41610518T>C | CA399490035 | KRT16 | c.1093A>G (p.Lys365Glu) c.379A>G (p.Lys127Glu) | |
| 17 | g.41610518T>G | CA399490036 | KRT16 | c.1093A>C (p.Lys365Gln) c.379A>C (p.Lys127Gln) | |
| 17 | g.41610519G>A | CA500205996 | KRT16 | c.1092C>T (p.Thr364=) c.378C>T (p.Thr126=) | |
| 17 | g.41610519G>C | CA500205997 | KRT16 | c.1092C>G (p.Thr364=) c.378C>G (p.Thr126=) | |
| 17 | g.41610519G>T | CA500205998 | KRT16 | c.1092C>A (p.Thr364=) c.378C>A (p.Thr126=) | |
| 17 | g.41610520G>A | CA399490038 | KRT16 | c.1091C>T (p.Thr364Ile) c.377C>T (p.Thr126Ile) | gnomAD v4 |
| 17 | g.41610520G>C | CA399490040 | KRT16 | c.1091C>G (p.Thr364Ser) c.377C>G (p.Thr126Ser) | COSMIC |
| 17 | g.41610520G>T | CA399490041 | KRT16 | c.1091C>A (p.Thr364Asn) c.377C>A (p.Thr126Asn) | |
| 17 | g.41610521T>A | CA399490044 | KRT16 | c.1090A>T (p.Thr364Ser) c.376A>T (p.Thr126Ser) | |
| 17 | g.41610521T>C | CA399490046 | KRT16 | c.1090A>G (p.Thr364Ala) c.376A>G (p.Thr126Ala) | |
| 17 | g.41610521T>G | CA399490045 | KRT16 | c.1090A>C (p.Thr364Pro) c.376A>C (p.Thr126Pro) | |
| 17 | g.41610522C>A | CA399490048 | KRT16 | c.1089G>T (p.Glu363Asp) c.375G>T (p.Glu125Asp) | |
| 17 | g.41610522C= | CA2260098771 | KRT16 | c.1089G= (p.Glu363=) c.375G= (p.Glu125=) | |
| 17 | g.41610522C>G | CA399490049 | KRT16 | c.1089G>C (p.Glu363Asp) c.375G>C (p.Glu125Asp) | |
| 17 | g.41610522C>T | CA500205999 | KRT16 | c.1089G>A (p.Glu363=) c.375G>A (p.Glu125=) | dbSNP gnomAD v4 |
| 17 | g.41610523T>A | CA399490051 | KRT16 | c.1088A>T (p.Glu363Val) c.374A>T (p.Glu125Val) | |
| 17 | g.41610523T>C | CA399490053 | KRT16 | c.1088A>G (p.Glu363Gly) c.374A>G (p.Glu125Gly) | |
| 17 | g.41610523T>G | CA399490054 | KRT16 | c.1088A>C (p.Glu363Ala) c.374A>C (p.Glu125Ala) | |
| 17 | g.41610524C>A | CA399490056 | KRT16 | c.1087G>T (p.Glu363Ter) c.373G>T (p.Glu125Ter) | |
| 17 | g.41610524C= | CA2260098772 | KRT16 | c.1087G= (p.Glu363=) c.373G= (p.Glu125=) | |
| 17 | g.41610524C>G | CA399490058 | KRT16 | c.1087G>C (p.Glu363Gln) c.373G>C (p.Glu125Gln) | |
| 17 | g.41610524C>T | CA399490060 | KRT16 | c.1087G>A (p.Glu363Lys) c.373G>A (p.Glu125Lys) | dbSNP |
| 17 | g.41610525C>A | CA8562994 | KRT16 | c.1086G>T (p.Glu362Asp) c.372G>T (p.Glu124Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610525C= | CA2260098773 | KRT16 | c.1086G= (p.Glu362=) c.372G= (p.Glu124=) | |
| 17 | g.41610525C>G | CA399490062 | KRT16 | c.1086G>C (p.Glu362Asp) c.372G>C (p.Glu124Asp) | |
| 17 | g.41610525C>T | CA8562995 | KRT16 | c.1086G>A (p.Glu362=) c.372G>A (p.Glu124=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610526T>A | CA399490065 | KRT16 | c.1085A>T (p.Glu362Val) c.371A>T (p.Glu124Val) | |
| 17 | g.41610526T>C | CA399490068 | KRT16 | c.1085A>G (p.Glu362Gly) c.371A>G (p.Glu124Gly) | |
| 17 | g.41610526T>G | CA399490067 | KRT16 | c.1085A>C (p.Glu362Ala) c.371A>C (p.Glu124Ala) | |
| 17 | g.41610527C>A | CA399490070 | KRT16 | c.1084G>T (p.Glu362Ter) c.370G>T (p.Glu124Ter) | gnomAD v4 |
| 17 | g.41610527C= | CA2260098774 | KRT16 | c.1084G= (p.Glu362=) c.370G= (p.Glu124=) | |
| 17 | g.41610527C>G | CA399490072 | KRT16 | c.1084G>C (p.Glu362Gln) c.370G>C (p.Glu124Gln) | |
| 17 | g.41610527C>T | CA399490073 | KRT16 | c.1084G>A (p.Glu362Lys) c.370G>A (p.Glu124Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610528C>A | CA500206000 | KRT16 | c.1083G>T (p.Leu361=) c.369G>T (p.Leu123=) | |
| 17 | g.41610528C= | CA2260098775 | KRT16 | c.1083G= (p.Leu361=) c.369G= (p.Leu123=) | |
| 17 | g.41610528C>G | CA500206001 | KRT16 | c.1083G>C (p.Leu361=) c.369G>C (p.Leu123=) | |
| 17 | g.41610528C>T | CA500206002 | KRT16 | c.1083G>A (p.Leu361=) c.369G>A (p.Leu123=) | dbSNP gnomAD v4 |
| 17 | g.41610529A>C | CA399490076 | KRT16 | c.1082T>G (p.Leu361Arg) c.368T>G (p.Leu123Arg) | |
| 17 | g.41610529A>G | CA399490077 | KRT16 | c.1082T>C (p.Leu361Pro) c.368T>C (p.Leu123Pro) | |
| 17 | g.41610529A>T | CA399490079 | KRT16 | c.1082T>A (p.Leu361Gln) c.368T>A (p.Leu123Gln) | |
| 17 | g.41610530G>A | CA500206003 | KRT16 | c.1081C>T (p.Leu361=) c.367C>T (p.Leu123=) | |
| 17 | g.41610530G>C | CA399490081 | KRT16 | c.1081C>G (p.Leu361Val) c.367C>G (p.Leu123Val) | |
| 17 | g.41610530G= | CA2260098776 | KRT16 | c.1081C= (p.Leu361=) c.367C= (p.Leu123=) | |
| 17 | g.41610530G>T | CA399490082 | KRT16 | c.1081C>A (p.Leu361Met) c.367C>A (p.Leu123Met) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41610531G>A | CA500206004 | KRT16 | c.1080C>T (p.Ser360=) c.366C>T (p.Ser122=) | gnomAD v4 |
| 17 | g.41610531G>C | CA399490084 | KRT16 | c.1080C>G (p.Ser360Arg) c.366C>G (p.Ser122Arg) | |
| 17 | g.41610531G>T | CA399490086 | KRT16 | c.1080C>A (p.Ser360Arg) c.366C>A (p.Ser122Arg) | gnomAD v4 |
| 17 | g.41610532C>A | CA399490088 | KRT16 | c.1079G>T (p.Ser360Ile) c.365G>T (p.Ser122Ile) | |
| 17 | g.41610532C>G | CA399490090 | KRT16 | c.1079G>C (p.Ser360Thr) c.365G>C (p.Ser122Thr) | |
| 17 | g.41610532C>T | CA399490091 | KRT16 | c.1079G>A (p.Ser360Asn) c.365G>A (p.Ser122Asn) | gnomAD v4 |
| 17 | g.41610533T>A | CA399490094 | KRT16 | c.1078A>T (p.Ser360Cys) c.364A>T (p.Ser122Cys) | |
| 17 | g.41610533T>C | CA399490098 | KRT16 | c.1078A>G (p.Ser360Gly) c.364A>G (p.Ser122Gly) | |
| 17 | g.41610533T>G | CA399490096 | KRT16 | c.1078A>C (p.Ser360Arg) c.364A>C (p.Ser122Arg) | |
| 17 | g.41610534G>A | CA500206005 | KRT16 | c.1077C>T (p.Asn359=) c.363C>T (p.Asn121=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610534G>C | CA399490099 | KRT16 | c.1077C>G (p.Asn359Lys) c.363C>G (p.Asn121Lys) | |
| 17 | g.41610534G= | CA2260098777 | KRT16 | c.1077C= (p.Asn359=) c.363C= (p.Asn121=) | |
| 17 | g.41610534G>T | CA399490101 | KRT16 | c.1077C>A (p.Asn359Lys) c.363C>A (p.Asn121Lys) | |
| 17 | g.41610535T>A | CA399490103 | KRT16 | c.1076A>T (p.Asn359Ile) c.362A>T (p.Asn121Ile) | |
| 17 | g.41610535T>C | CA399490105 | KRT16 | c.1076A>G (p.Asn359Ser) c.362A>G (p.Asn121Ser) | |
| 17 | g.41610535T>G | CA399490107 | KRT16 | c.1076A>C (p.Asn359Thr) c.362A>C (p.Asn121Thr) | COSMIC |
| 17 | g.41610536T>A | CA399490108 | KRT16 | c.1075A>T (p.Asn359Tyr) c.361A>T (p.Asn121Tyr) | |
| 17 | g.41610536T>C | CA399490110 | KRT16 | c.1075A>G (p.Asn359Asp) c.361A>G (p.Asn121Asp) | |
| 17 | g.41610536T>G | CA399490112 | KRT16 | c.1075A>C (p.Asn359His) c.361A>C (p.Asn121His) | |
| 17 | g.41610537C>A | CA399490114 | KRT16 | c.1074G>T (p.Glu358Asp) c.360G>T (p.Glu120Asp) | |
| 17 | g.41610537C>G | CA399490116 | KRT16 | c.1074G>C (p.Glu358Asp) c.360G>C (p.Glu120Asp) | |
| 17 | g.41610537C>T | CA500206006 | KRT16 | c.1074G>A (p.Glu358=) c.360G>A (p.Glu120=) | gnomAD v4 |
| 17 | g.41610538T>A | CA399490119 | KRT16 | c.1073A>T (p.Glu358Val) c.359A>T (p.Glu120Val) | |
| 17 | g.41610538T>C | CA399490121 | KRT16 | c.1073A>G (p.Glu358Gly) c.359A>G (p.Glu120Gly) | COSMIC |
| 17 | g.41610538T>G | CA399490117 | KRT16 | c.1073A>C (p.Glu358Ala) c.359A>C (p.Glu120Ala) | |
| 17 | g.41610539C>A | CA399490126 | KRT16 | c.1072G>T (p.Glu358Ter) c.358G>T (p.Glu120Ter) | |
| 17 | g.41610539C>G | CA399490122 | KRT16 | c.1072G>C (p.Glu358Gln) c.358G>C (p.Glu120Gln) | |
| 17 | g.41610539C>T | CA399490124 | KRT16 | c.1072G>A (p.Glu358Lys) c.358G>A (p.Glu120Lys) | |
| 17 | g.41610540C>A | CA500206008 | KRT16 | c.1071G>T (p.Leu357=) c.357G>T (p.Leu119=) | |
| 17 | g.41610540C= | CA2260098778 | KRT16 | c.1071G= (p.Leu357=) c.357G= (p.Leu119=) | |
| 17 | g.41610540C>G | CA500206007 | KRT16 | c.1071G>C (p.Leu357=) c.357G>C (p.Leu119=) | |
| 17 | g.41610540C>T | CA290676177 | KRT16 | c.1071G>A (p.Leu357=) c.357G>A (p.Leu119=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 17 | g.41610541A>C | CA399490128 | KRT16 | c.1070T>G (p.Leu357Arg) c.356T>G (p.Leu119Arg) | |
| 17 | g.41610541A>G | CA399490129 | KRT16 | c.1070T>C (p.Leu357Pro) c.356T>C (p.Leu119Pro) | |
| 17 | g.41610541A>T | CA399490130 | KRT16 | c.1070T>A (p.Leu357Gln) c.356T>A (p.Leu119Gln) | |
| 17 | g.41610542G>A | CA500206009 | KRT16 | c.1069C>T (p.Leu357=) c.355C>T (p.Leu119=) | |
| 17 | g.41610542G>C | CA399490133 | KRT16 | c.1069C>G (p.Leu357Val) c.355C>G (p.Leu119Val) | |
| 17 | g.41610542G>T | CA399490131 | KRT16 | c.1069C>A (p.Leu357Met) c.355C>A (p.Leu119Met) | |
| 17 | g.41610543G>A | CA500206010 | KRT16 | c.1068C>T (p.Ser356=) c.354C>T (p.Ser118=) | |
| 17 | g.41610543G>C | CA500206011 | KRT16 | c.1068C>G (p.Ser356=) c.354C>G (p.Ser118=) | |
| 17 | g.41610543G>T | CA500206012 | KRT16 | c.1068C>A (p.Ser356=) c.354C>A (p.Ser118=) | gnomAD v4 |
| 17 | g.41610544G>A | CA399490134 | KRT16 | c.1067C>T (p.Ser356Phe) c.353C>T (p.Ser118Phe) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41610544G>C | CA399490135 | KRT16 | c.1067C>G (p.Ser356Cys) c.353C>G (p.Ser118Cys) | |
| 17 | g.41610544G= | CA2260098779 | KRT16 | c.1067C= (p.Ser356=) c.353C= (p.Ser118=) | |
| 17 | g.41610544G>T | CA399490137 | KRT16 | c.1067C>A (p.Ser356Tyr) c.353C>A (p.Ser118Tyr) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.41610545A>C | CA399490138 | KRT16 | c.1066T>G (p.Ser356Ala) c.352T>G (p.Ser118Ala) | |
| 17 | g.41610545A>G | CA399490140 | KRT16 | c.1066T>C (p.Ser356Pro) c.352T>C (p.Ser118Pro) | ClinVar |
| 17 | g.41610545A>T | CA399490142 | KRT16 | c.1066T>A (p.Ser356Thr) c.352T>A (p.Ser118Thr) | |
| 17 | g.41610546T>A | CA500206013 | KRT16 | c.1065A>T (p.Ala355=) c.351A>T (p.Ala117=) | |
| 17 | g.41610546T>C | CA500206014 | KRT16 | c.1065A>G (p.Ala355=) c.351A>G (p.Ala117=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.41610546T>G | CA500206015 | KRT16 | c.1065A>C (p.Ala355=) c.351A>C (p.Ala117=) | gnomAD v4 |
| 17 | g.41610546T= | CA2260098780 | KRT16 | c.1065A= (p.Ala355=) c.351A= (p.Ala117=) | |
| 17 | g.41610547G>A | CA8562996 | KRT16 | c.1064C>T (p.Ala355Val) c.350C>T (p.Ala117Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.41610547G>C | CA399490147 | KRT16 | c.1064C>G (p.Ala355Gly) c.350C>G (p.Ala117Gly) | |
| 17 | g.41610547G= | CA2260098781 | KRT16 | c.1064C= (p.Ala355=) c.350C= (p.Ala117=) | |
| 17 | g.41610547G>T | CA399490145 | KRT16 | c.1064C>A (p.Ala355Glu) c.350C>A (p.Ala117Glu) | gnomAD v4 |
| 17 | g.41610548C>A | CA399490148 | KRT16 | c.1063G>T (p.Ala355Ser) c.349G>T (p.Ala117Ser) | dbSNP gnomAD v4 COSMIC |
| 17 | g.41610548C= | CA2260098782 | KRT16 | c.1063G= (p.Ala355=) c.349G= (p.Ala117=) | |
| 17 | g.41610548C>G | CA399490150 | KRT16 | c.1063G>C (p.Ala355Pro) c.349G>C (p.Ala117Pro) | |
| 17 | g.41610548C>T | CA8562997 | KRT16 | c.1063G>A (p.Ala355Thr) c.349G>A (p.Ala117Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610549T>A | CA217370 | KRT16 | c.1062A>T (p.Lys354Asn) c.348A>T (p.Lys116Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.41610549T>C | CA500206016 | KRT16 | c.1062A>G (p.Lys354=) c.348A>G (p.Lys116=) | |
| 17 | g.41610549T>G | CA399490153 | KRT16 | c.1062A>C (p.Lys354Asn) c.348A>C (p.Lys116Asn) | |
| 17 | g.41610549T= | CA2260098783 | KRT16 | c.1062A= (p.Lys354=) c.348A= (p.Lys116=) |