Colon Cancer: Gene >> GSTA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334575
Start	52794192:52794192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347A>G
AA Mutation	p.Glu116Gly(p.E116G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334575
Start	52796188:52796188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1131849
CDS Mutation	c.266G>A
AA Mutation	p.Arg89Lys(p.R89K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334575
Start	52796273:52796273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Asp61Asn(p.D61N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334575
Start	52791934:52791934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593T>C
AA Mutation	p.Leu198Pro(p.L198P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334575
Start	52792951:52792951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451A>G
AA Mutation	p.Asn151Asp(p.N151D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334575
Start	52792940:52792940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334575
Start	52796229:52796229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GSTA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334575
Start	52791884:52791884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>A
AA Mutation	p.Glu215Lys(p.E215K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript