Colon Cancer: Gene >> GSTA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000211122
Start	52900003:52900003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345G>T
AA Mutation	p.Glu115Asp(p.E115D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000211122
Start	52902473:52902473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145A>C
AA Mutation	p.Ser49Arg(p.S49R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000211122
Start	52896853:52896853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45620832
CDS Mutation	c.622G>A
AA Mutation	p.Ala208Thr(p.A208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000211122
Start	52896890:52896890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585G>T
AA Mutation	p.Lys195Asn(p.K195N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000211122
Start	52896821:52896821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654G>T
AA Mutation	p.Lys218Asn(p.K218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000211122
Start	52900011:52900011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779762341
CDS Mutation	c.337C>T
AA Mutation	p.Arg113Ter(p.R113*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GSTA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000211122
Start	52903687:52903687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128A>C
AA Mutation	p.Lys43Thr(p.K43T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000211122
Start	52902375:52902375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243C>A
Mutation Classification	Silent
Feature Type	Transcript