Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> STRADB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000194530
Start	201477728:201477728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658T>C
AA Mutation	p.Tyr220His(p.Y220H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000194530
Start	201477729:201477729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659A>G
AA Mutation	p.Tyr220Cys(p.Y220C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000194530
Start	201480137:201480137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1219G>T
AA Mutation	p.Asp407Tyr(p.D407Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STRADB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000194530
Start	201473012:201473012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251C>T
AA Mutation	p.Thr84Ile(p.T84I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000194530
Start	201478596:201478596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1065G>T
AA Mutation	p.Glu355Asp(p.E355D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000194530
Start	201470025:201470025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166T>A
AA Mutation	p.Ser56Thr(p.S56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript