Colon Cancer: Gene >> SNAI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000020945
Start	48918831:48918831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783A>T
AA Mutation	p.Glu261Asp(p.E261D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000020945
Start	48920432:48920432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89C>T
AA Mutation	p.Ser30Phe(p.S30F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000020945
Start	48921206:48921206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000020945
Start	48920068:48920068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SNAI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000020945
Start	48920099:48920099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422C>T
AA Mutation	p.Ser141Phe(p.S141F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000020945
Start	48920284:48920284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549411169
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript