Colon Cancer: Gene >> GSTM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241337
Start	109671315:109671315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389C>G
AA Mutation	p.Ala130Gly(p.A130G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241337
Start	109668140:109668140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25A>G
AA Mutation	p.Asn9Asp(p.N9D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241337
Start	109671371:109671371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445C>A
AA Mutation	p.Leu149Ile(p.L149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241337
Start	109668463:109668463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>A
AA Mutation	p.Asp25Glu(p.D25E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241337
Start	109674759:109674759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580A>T
AA Mutation	p.Ile194Phe(p.I194F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000241337
Start	109668924:109668924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GSTM2

No Mutation Annotation!