Putative Neo-Functional Events (NFEs)
Browse Information on NFEs in FunVar
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Showing 15001 to 15020 of 19604 entries
Cancer Mutation Type UniProtKB Location Mutation PDB Res FunFam Links View
UCEC Missense Mutation Q14118 E→G 1u2c:A:116 Dystroglycan 1
2.60.40.10-FF-133792 		UniProtKB InterPro GO
UCEC Missense Mutation Q14118 E→G 1u2c:A:116 Dystroglycan 1
2.60.40.10-FF-133792 		UniProtKB InterPro GO
SKCM Missense Mutation Q14126 S→F 1edh:A:147 Cadherin 3, type 1, P-cadherin
2.60.40.60-FF-18813 		UniProtKB InterPro GO
SKCM Missense Mutation Q14126 S→F 1edh:A:147 Cadherin 3, type 1, P-cadherin
2.60.40.60-FF-18813 		UniProtKB InterPro GO
COAD Missense Mutation Q14155 R→H 1by1:A:151 Rho guanine nucleotide exchange factor 7
1.20.900.10-FF-3298 		UniProtKB InterPro GO
COAD Missense Mutation Q14155 R→H 1by1:A:151 Rho guanine nucleotide exchange factor 7
1.20.900.10-FF-3298 		UniProtKB InterPro GO
UCEC Missense Mutation Q14155 R→H 1by1:A:151 Rho guanine nucleotide exchange factor 7
1.20.900.10-FF-3298 		UniProtKB InterPro GO
UCEC Missense Mutation Q14155 R→H 1by1:A:151 Rho guanine nucleotide exchange factor 7
1.20.900.10-FF-3298 		UniProtKB InterPro GO
UCEC Missense Mutation Q14155 K→N 1by1:A:154 Rho guanine nucleotide exchange factor 7
1.20.900.10-FF-3298 		UniProtKB InterPro GO
UCEC Missense Mutation Q14155 K→N 1by1:A:154 Rho guanine nucleotide exchange factor 7
1.20.900.10-FF-3298 		UniProtKB InterPro GO
UCEC Missense Mutation Q14186 E→K 1cf7:B:92 Transcription factor Dp-2, putative
1.10.10.10-FF-264734 		UniProtKB InterPro GO
UCEC Missense Mutation Q14186 E→K 1cf7:B:92 Transcription factor Dp-2, putative
1.10.10.10-FF-264734 		UniProtKB InterPro GO
LUAD Missense Mutation Q14191 Q→H 2dgz:A:1165 Werner syndrome ATP-dependent helicase
1.10.150.80-FF-3214 		UniProtKB InterPro GO
LUAD Missense Mutation Q14191 Q→H 2dgz:A:1165 Werner syndrome ATP-dependent helicase
1.10.150.80-FF-3214 		UniProtKB InterPro GO
SKCM Missense Mutation Q14191 S→F 2fbt:A:194 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
SKCM Missense Mutation Q14191 S→F 2fbt:A:194 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
PAAD Missense Mutation Q14191 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
PAAD Missense Mutation Q14191 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
UCEC Missense Mutation Q14191 S→R 2fbt:A:198 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
UCEC Missense Mutation Q14191 S→R 2fbt:A:198 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO