Colon Cancer: Gene >> SMOC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356284
Start	168509964:168509964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141002558
CDS Mutation	c.134C>T
AA Mutation	p.Ala45Val(p.A45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356284
Start	168598979:168598979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776824810
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Cys(p.R267C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356284
Start	168653201:168653201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201624579
CDS Mutation	c.1258G>A
AA Mutation	p.Gly420Ser(p.G420S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356284
Start	168598904:168598904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724C>T
AA Mutation	p.His242Tyr(p.H242Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356284
Start	168598825:168598825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356284
Start	168653074:168653074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1131G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SMOC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356284
Start	168598910:168598910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561879643
CDS Mutation	c.730G>A
AA Mutation	p.Gly244Ser(p.G244S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356284
Start	168608169:168608169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376609544
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript