Colon Cancer: Gene >> RPS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343262
Start	1962586:1962586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620C>T
AA Mutation	p.Ala207Val(p.A207V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343262
Start	1962129:1962129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367578393
CDS Mutation	c.851G>A
AA Mutation	p.Arg284Gln(p.R284Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343262
Start	1962252:1962252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728C>T
AA Mutation	p.Ala243Val(p.A243V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343262
Start	1963209:1963209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000343262
Start	1964274:1964274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RPS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343262
Start	1962626:1962626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580C>T
AA Mutation	p.Arg194Cys(p.R194C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript