Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RNF26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311413
Start	119335339:119335339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217G>A
AA Mutation	p.Val73Ile(p.V73I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311413
Start	119335513:119335513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752881562
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Cys(p.R131C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311413
Start	119335774:119335774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771435796
CDS Mutation	c.652C>T
AA Mutation	p.Arg218Cys(p.R218C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311413
Start	119335297:119335297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175C>T
AA Mutation	p.Arg59Cys(p.R59C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311413
Start	119335879:119335879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311413
Start	119335263:119335263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311413
Start	119336409:119336409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNF26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311413
Start	119335432:119335432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775259101
CDS Mutation	c.310G>A
AA Mutation	p.Ala104Thr(p.A104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311413
Start	119335269:119335269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311413
Start	119335263:119335263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript