Colon Cancer: Gene >> GSTZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216465
Start	77326868:77326868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750964006
CDS Mutation	c.98C>T
AA Mutation	p.Thr33Met(p.T33M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216465
Start	77324879:77324879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25T>C
AA Mutation	p.Tyr9His(p.Y9H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216465
Start	77324874:77324874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20T>A
AA Mutation	p.Ile7Asn(p.I7N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216465
Start	77330346:77330346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>A
AA Mutation	p.Ala171Thr(p.A171T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000216465
Start	77324915:77324915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758377745
CDS Mutation	c.61C>T
AA Mutation	p.Arg21Ter(p.R21*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000216465
Start	77327911:77327911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GSTZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216465
Start	77331148:77331148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604T>C
AA Mutation	p.Ser202Pro(p.S202P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000216465
Start	77324915:77324915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758377745
CDS Mutation	c.61C>T
AA Mutation	p.Arg21Ter(p.R21*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript