Colon Cancer: Gene >> DDC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357936
Start	50479852:50479852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>T
AA Mutation	p.Arg319Ile(p.R319I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357936
Start	50470104:50470104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1109G>A
AA Mutation	p.Gly370Glu(p.G370E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357936
Start	50539939:50539939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357936
Start	50463377:50463377(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1297delA
AA Mutation	p.Ile433SerfsTer98(p.I433Sfs*98)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DDC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357936
Start	50543991:50543991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95A>T
AA Mutation	p.Asp32Val(p.D32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357936
Start	50476625:50476625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040G>T
AA Mutation	p.Arg347Leu(p.R347L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript