Putative Neo-Functional Events (NFEs)
Browse Information on NFEs in FunVar
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Showing 18701 to 18720 of 19604 entries
Cancer Mutation Type UniProtKB Location Mutation PDB Res FunFam Links View
COAD Missense Mutation Q9NV35 Y→D 5bon:A:92 Probable 8-oxo-dGTP diphosphatase NUDT15
3.90.79.10-FF-21641 		UniProtKB InterPro GO
COAD Missense Mutation Q9NV35 Y→D 5bon:A:92 Probable 8-oxo-dGTP diphosphatase NUDT15
3.90.79.10-FF-21641 		UniProtKB InterPro GO
CESC Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
CESC Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
HNSC Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
HNSC Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
LUAD Missense Mutation Q9NVH0 R→G 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
LUAD Missense Mutation Q9NVH0 R→G 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
SKCM Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
SKCM Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
SKCM Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
SKCM Missense Mutation Q9NVH0 R→C 2fbt:A:196 Werner syndrome ATP-dependent helicase
3.30.420.10-FF-45955 		UniProtKB InterPro GO
UCEC Missense Mutation Q9NVS9 R→C 1nrg:A:138 Protein Bm4511, isoform b
2.30.110.10-FF-14392 		UniProtKB InterPro GO
UCEC Missense Mutation Q9NVS9 R→C 1nrg:A:138 Protein Bm4511, isoform b
2.30.110.10-FF-14392 		UniProtKB InterPro GO
UCEC Missense Mutation Q9NVS9 R→C 1nrg:A:138 Protein Bm4511, isoform b
2.30.110.10-FF-14392 		UniProtKB InterPro GO
UCEC Missense Mutation Q9NVS9 R→C 1nrg:A:138 Protein Bm4511, isoform b
2.30.110.10-FF-14392 		UniProtKB InterPro GO
BRCA Missense Mutation Q9NVS9 E→K 1nrg:A:68 Protein Bm4511, isoform b
2.30.110.10-FF-14392 		UniProtKB InterPro GO
BRCA Missense Mutation Q9NVS9 E→K 1nrg:A:68 Protein Bm4511, isoform b
2.30.110.10-FF-14392 		UniProtKB InterPro GO
STAD Missense Mutation Q9NW64 R→W 2ytc:A:284 Pre-mRNA-splicing factor SLT11, putative
3.30.70.330-FF-43715 		UniProtKB InterPro GO
STAD Missense Mutation Q9NW64 R→W 2ytc:A:284 Pre-mRNA-splicing factor SLT11, putative
3.30.70.330-FF-43715 		UniProtKB InterPro GO