Colon Cancer: Gene >> FRS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397997
Start	69574735:69574735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307A>G
AA Mutation	p.Tyr436Cys(p.Y436C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397997
Start	69574362:69574362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000397997
Start	69574311:69574311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883C>T
AA Mutation	p.Arg295Ter(p.R295*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000397997
Start	69572117:69572117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FRS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397997
Start	69571381:69571381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359G>T
AA Mutation	p.Arg120Ile(p.R120I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397997
Start	69574398:69574398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550828203
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Cys(p.R324C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript