Colon Cancer: Gene >> RPL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307961
Start	66499585:66499585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106C>T
AA Mutation	p.Ala369Val(p.A369V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307961
Start	66502744:66502744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752263296
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Cys(p.R97C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307961
Start	66503496:66503496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780532132
CDS Mutation	c.37G>A
AA Mutation	p.Glu13Lys(p.E13K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307961
Start	66499476:66499476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1215G>T
AA Mutation	p.Lys405Asn(p.K405N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307961
Start	66500990:66500990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752785467
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307961
Start	66501488:66501488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776481741
CDS Mutation	c.563G>A
AA Mutation	p.Arg188Gln(p.R188Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript