Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RPL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92836239:92836239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374T>C
AA Mutation	p.Val125Ala(p.V125A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92837547:92837547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746120360
CDS Mutation	c.619T>C
AA Mutation	p.Tyr207His(p.Y207H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92841848:92841848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200315052
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Trp(p.R293W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92834833:92834833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Glu82Lys(p.E82K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92834824:92834824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235T>C
AA Mutation	p.Tyr79His(p.Y79H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RPL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92840619:92840619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>T
AA Mutation	p.Lys258Asn(p.K258N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92833614:92833614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143A>C
AA Mutation	p.Lys48Thr(p.K48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370321
Start	92841774:92841774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765443248
CDS Mutation	c.803G>A
AA Mutation	p.Arg268His(p.R268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript