Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HMGCS2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369406
Start 119752627:119752627(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61729865
CDS Mutation c.1342C>T
AA Mutation p.Arg448Cys(p.R448C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000369406
Start 119757274:119757274(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775277893
CDS Mutation c.1015G>A
AA Mutation p.Gly339Arg(p.G339R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369406
Start 119752603:119752603(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1366T>C
AA Mutation p.Ser456Pro(p.S456P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369406
Start 119759932:119759932(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.617G>A
AA Mutation p.Arg206His(p.R206H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000369406
Start 119759139:119759139(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.829delA
AA Mutation p.Ile277SerfsTer22(p.I277Sfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000369406
Start 119753304:119753304(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs137852637
CDS Mutation c.1270C>T
AA Mutation p.Arg424Ter(p.R424*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> HMGCS2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369406
Start 119768765:119768765(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757169217
CDS Mutation c.80G>A
AA Mutation p.Arg27His(p.R27H)
Mutation Classification Missense_Mutation
Feature Type Transcript