Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAZ

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000322945
Start 29807390:29807390(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.605G>A
AA Mutation p.Gly202Asp(p.G202D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000322945
Start 29806732:29806732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.31G>C
AA Mutation p.Ala11Pro(p.A11P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000322945
Start 29810120:29810120(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370548510
CDS Mutation c.1323G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000322945
Start 29808663:29808663(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs1043766
CDS Mutation c.1201C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000322945
Start 29806879:29806879(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.178C>T
AA Mutation p.Gln60Ter(p.Q60*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> MAZ

Mutation ID 1
Mutation Consequence inframe_deletion
Transcription ID ENST00000322945
Start 29810109:29810117(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs780065474
CDS Mutation c.1323_1331delGGCAGCGGC
AA Mutation p.Ala446_Ala448del(p.A446_A448del)
Mutation Classification In_Frame_Del
Feature Type Transcript