Colon Cancer: Gene >> NPY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242152
Start	24285365:24285365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125C>T
AA Mutation	p.Ala42Val(p.A42V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242152
Start	24285398:24285398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158G>A
AA Mutation	p.Arg53Gln(p.R53Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242152
Start	24285357:24285357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242152
Start	24285318:24285318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242152
Start	24285312:24285312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000242152
Start	24285397:24285397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Ter(p.R53*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NPY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242152
Start	24291681:24291681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288G>A
AA Mutation	p.Met96Ile(p.M96I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript