Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IL7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263851
Start	78736480:78736480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408G>T
AA Mutation	p.Lys136Asn(p.K136N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263851
Start	78740039:78740039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191T>G
AA Mutation	p.Phe64Cys(p.F64C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263851
Start	78733775:78733775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472A>G
AA Mutation	p.Arg158Gly(p.R158G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263851
Start	78733798:78733798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449T>G
AA Mutation	p.Leu150Arg(p.L150R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263851
Start	78798186:78798186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263851
Start	78738630:78738630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000263851
Start	78740070:78740070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>T
AA Mutation	p.Glu54Ter(p.E54*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263851
Start	78736480:78736480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408G>T
AA Mutation	p.Lys136Asn(p.K136N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript