7953 NP_109597 Q523P not found in SNVbox database
Sequencing variant TCGA-EM-A2P1-06A-11D-A202-08 chr22:47059055 C>T maps to NM_015124.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P1-06A-11D-A202-08 chr22:47059055 C>T maps to NM_015124.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P1-06A-11D-A202-08 chr3:142037637 T>C maps to NM_019001.3 Q1503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P1-06A-11D-A202-08 chr3:142037637 T>C maps to NM_019001.3 Q1503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FQ-06A-11D-A21A-08 chr19:57176119 C>T maps to NM_001005850.1 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FQ-06A-11D-A21A-08 chr19:57176119 C>T maps to NM_001005850.1 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FQ-06A-11D-A21A-08 chr12:126138655 G>A maps to NM_052907.2 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FQ-06A-11D-A21A-08 chr12:126138655 G>A maps to NM_052907.2 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3YH-06A-11D-A23M-08 chr4:68925070 G>A maps to NM_207407.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3YH-06A-11D-A23M-08 chr4:68925070 G>A maps to NM_207407.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3YH-06A-11D-A23M-08 chr9:414952 T>A did not map to a codon.
Sequencing variant TCGA-J8-A3YH-06A-11D-A23M-08 chr9:414952 T>A did not map to a codon.
Sequencing variant TCGA-J8-A4HW-06A-11D-A257-08 chr18:20774480 G>A maps to NM_001100619.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A4HW-06A-11D-A257-08 chr18:20774480 G>A maps to NM_001100619.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A4HW-06A-11D-A257-08 chr12:113425105 C>T maps to NM_016817.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A4HW-06A-11D-A257-08 chr12:113425105 C>T maps to NM_016817.2 N147N. Only missense variants will be evaluated by CHASM.
