Colon Cancer: Gene >> GLS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311966
Start	56477963:56477963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750601118
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Cys(p.R250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311966
Start	56479057:56479057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529G>T
AA Mutation	p.Gly177Cys(p.G177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311966
Start	56488025:56488025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>A
AA Mutation	p.Leu32Ile(p.L32I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311966
Start	56480358:56480358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756555927
CDS Mutation	c.212G>A
AA Mutation	p.Arg71His(p.R71H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311966
Start	56471569:56471569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727A>T
AA Mutation	p.Gln576Leu(p.Q576L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311966
Start	56474667:56474667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145926460
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GLS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311966
Start	56471828:56471828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1597G>A
AA Mutation	p.Glu533Lys(p.E533K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000311966
Start	56471772:56471772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1652+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript