Colon Cancer: Gene >> GAL3ST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338911
Start	30555066:30555066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159G>A
AA Mutation	p.Ala387Thr(p.A387T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338911
Start	30555116:30555116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109C>A
AA Mutation	p.Thr370Asn(p.T370N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338911
Start	30555162:30555162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063G>A
AA Mutation	p.Ala355Thr(p.A355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338911
Start	30555725:30555725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500C>T
AA Mutation	p.Ala167Val(p.A167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338911
Start	30555769:30555769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338911
Start	30555886:30555886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GAL3ST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338911
Start	30555621:30555621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Cys(p.R202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000338911
Start	30557365:30557365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>T
AA Mutation	p.Glu10Ter(p.E10*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript