Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MICA

Mutation ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000449934
Start 31410670:31410670(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.198A>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000449934
Start 31411202:31411202(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.456G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000449934
Start 31412384:31412384(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs67841474
CDS Mutation c.953delG
AA Mutation p.Gly318AlafsTer68(p.G318Afs*68)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 4
Mutation Consequence inframe_deletion
Transcription ID ENST00000449934
Start 31412401:31412403(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.977_979delATT
AA Mutation p.Tyr326del(p.Y326del)
Mutation Classification In_Frame_Del
Feature Type Transcript

Rectum Cancer: Gene >> MICA

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000449934
Start 31410545:31410545(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.73C>T
AA Mutation p.Pro25Ser(p.P25S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000449934
Start 31412414:31412414(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.982C>A
AA Mutation p.Leu328Ile(p.L328I)
Mutation Classification Missense_Mutation
Feature Type Transcript