Colon Cancer: Gene >> GSTM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369836
Start	109658904:109658904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>T
AA Mutation	p.Asp151Tyr(p.D151Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369836
Start	109659103:109659103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375686135
CDS Mutation	c.560G>A
AA Mutation	p.Arg187His(p.R187H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369836
Start	109657249:109657249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147A>C
AA Mutation	p.Glu49Asp(p.E49D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369836
Start	109656760:109656760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Glu29Lys(p.E29K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000369836
Start	109656711:109656711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GSTM4

Mutation ID	1
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000369836
Start	109658910:109658910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript