Colon Cancer: Gene >> COASY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393818
Start	42563089:42563089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467A>G
AA Mutation	p.Tyr156Cys(p.Y156C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393818
Start	42564491:42564491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961C>A
AA Mutation	p.Leu321Ile(p.L321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393818
Start	42564555:42564555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025G>A
AA Mutation	p.Gly342Glu(p.G342E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393818
Start	42565700:42565700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775885531
CDS Mutation	c.1527C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000393818
Start	42565281:42565281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200491699
CDS Mutation	c.1357C>T
AA Mutation	p.Arg453Ter(p.R453*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> COASY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393818
Start	42562690:42562690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68C>T
AA Mutation	p.Ala23Val(p.A23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript