Colon Cancer: Gene >> GZMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216341
Start	24632100:24632100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142224147
CDS Mutation	c.358C>T
AA Mutation	p.Arg120Trp(p.R120W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216341
Start	24631079:24631079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.736C>A
AA Mutation	p.Arg246Ser(p.R246S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216341
Start	24631914:24631914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138221069
CDS Mutation	c.544G>A
AA Mutation	p.Asp182Asn(p.D182N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216341
Start	24631938:24631938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520G>A
AA Mutation	p.Glu174Lys(p.E174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216341
Start	24632022:24632022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757031846
CDS Mutation	c.436G>A
AA Mutation	p.Gly146Ser(p.G146S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216341
Start	24632971:24632971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141950099
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GZMB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216341
Start	24631939:24631939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61747598
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript