Colon Cancer: Gene >> RPL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216146
Start	39316836:39316836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371A>C
AA Mutation	p.Lys124Thr(p.K124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216146
Start	39314186:39314186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872A>G
AA Mutation	p.Tyr291Cys(p.Y291C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216146
Start	39316802:39316802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405G>T
AA Mutation	p.Lys135Asn(p.K135N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216146
Start	39313645:39313645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036A>G
AA Mutation	p.Thr346Ala(p.T346A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216146
Start	39316800:39316800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407A>C
AA Mutation	p.Lys136Thr(p.K136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216146
Start	39315397:39315397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765720761
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPL3

No Mutation Annotation!