Colon Cancer: Gene >> CNPY2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000273308
Start	56315132:56315132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>A
AA Mutation	p.Gly29Glu(p.G29E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273308
Start	56314942:56314942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113T>C
AA Mutation	p.Leu38Pro(p.L38P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273308
Start	56310564:56310564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CNPY2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273308
Start	56311010:56311010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453C>A
AA Mutation	p.Phe151Leu(p.F151L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273308
Start	56311392:56311392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>T
AA Mutation	p.Ala76Val(p.A76V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript