Colon Cancer: Gene >> STX8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306357
Start	9505130:9505130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>A
AA Mutation	p.Gly119Glu(p.G119E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306357
Start	9557453:9557453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193G>A
AA Mutation	p.Ala65Thr(p.A65T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306357
Start	9378603:9378603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752149374
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Cys(p.R198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306357
Start	9568408:9568408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140592918
CDS Mutation	c.80G>A
AA Mutation	p.Arg27Gln(p.R27Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306357
Start	9378607:9378607(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.588delA
AA Mutation	p.Lys196AsnfsTer9(p.K196Nfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STX8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306357
Start	9378603:9378603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752149374
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Cys(p.R198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306357
Start	9378622:9378622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573G>T
AA Mutation	p.Glu191Asp(p.E191D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript