Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> STX1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222812
Start	73702943:73702943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580G>A
AA Mutation	p.Glu194Lys(p.E194K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222812
Start	73702865:73702865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658G>A
AA Mutation	p.Ala220Thr(p.A220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222812
Start	73703771:73703771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524C>T
AA Mutation	p.Ala175Val(p.A175V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STX1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222812
Start	73704384:73704384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>A
AA Mutation	p.Arg108His(p.R108H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222812
Start	73702935:73702935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588G>T
AA Mutation	p.Glu196Asp(p.E196D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript