Colon Cancer: Gene >> PGC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373025
Start	41736857:41736857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162G>A
AA Mutation	p.Ala388Thr(p.A388T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373025
Start	41742432:41742432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505A>G
AA Mutation	p.Thr169Ala(p.T169A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373025
Start	41744450:41744450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275C>T
AA Mutation	p.Thr92Ile(p.T92I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373025
Start	41744428:41744428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768818702
CDS Mutation	c.297G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373025
Start	41744461:41744461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373025
Start	41736926:41736926(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1093delG
AA Mutation	p.Asp365MetfsTer18(p.D365Mfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373025
Start	41744429:41744430(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.295dupG
AA Mutation	p.Val99GlyfsTer48(p.V99Gfs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PGC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373025
Start	41744403:41744403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770437031
CDS Mutation	c.322G>A
AA Mutation	p.Ala108Thr(p.A108T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript