Colon Cancer: Gene >> RRAS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256196
Start	14294530:14294530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782490571
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Cys(p.R117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256196
Start	14281657:14281657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472G>A
AA Mutation	p.Ala158Thr(p.A158T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256196
Start	14279352:14279352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RRAS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256196
Start	14281630:14281630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499G>A
AA Mutation	p.Ala167Thr(p.A167T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256196
Start	14295820:14295820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144A>C
AA Mutation	p.Glu48Asp(p.E48D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256196
Start	14295819:14295819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>T
AA Mutation	p.Asp49Tyr(p.D49Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript