Colon Cancer: Gene >> RPS23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296674
Start	82277741:82277741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116A>C
AA Mutation	p.Asn39Thr(p.N39T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296674
Start	82276450:82276450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233G>A
AA Mutation	p.Gly78Asp(p.G78D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296674
Start	82277759:82277759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772924662
CDS Mutation	c.98G>A
AA Mutation	p.Gly33Asp(p.G33D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296674
Start	82276430:82276430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>T
AA Mutation	p.Val85Leu(p.V85L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296674
Start	82276223:82276223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPS23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296674
Start	82277769:82277769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88G>A
AA Mutation	p.Ala30Thr(p.A30T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript