Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392369
Start	130875903:130875903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628C>A
AA Mutation	p.Pro210Thr(p.P210T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392369
Start	130875718:130875718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542C>T
AA Mutation	p.Ala181Val(p.A181V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392369
Start	130875723:130875723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>A
AA Mutation	p.Ala183Thr(p.A183T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392369
Start	130874717:130874717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419G>A
AA Mutation	p.Arg140Gln(p.R140Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392369
Start	130872599:130872599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392369
Start	130872894:130872894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11546492
CDS Mutation	c.95C>T
AA Mutation	p.Thr32Ile(p.T32I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392369
Start	130874678:130874678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380A>C
AA Mutation	p.Lys127Thr(p.K127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000392369
Start	130872835:130872835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript