Colon Cancer: Gene >> MGST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000010404
Start	16354287:16354287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.35T>A
AA Mutation	p.Val12Glu(p.V12E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000010404
Start	16357678:16357678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762233825
CDS Mutation	c.200A>G
AA Mutation	p.Asp67Gly(p.D67G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000010404
Start	16363881:16363881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>T
AA Mutation	p.Ala103Val(p.A103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000010404
Start	16363972:16363972(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.405delT
AA Mutation	p.Phe135LeufsTer15(p.F135Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MGST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000010404
Start	16357669:16357669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764640311
CDS Mutation	c.191G>A
AA Mutation	p.Arg64Gln(p.R64Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000010404
Start	16354230:16354230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-22-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000010404
Start	16354379:16354379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript