Colon Cancer: Gene >> GZMH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216338
Start	24607701:24607701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Trp(p.R84W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216338
Start	24608361:24608361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107C>T
AA Mutation	p.Ala36Val(p.A36V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216338
Start	24607373:24607373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148085251
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Trp(p.R125W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216338
Start	24608373:24608373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766652570
CDS Mutation	c.95G>A
AA Mutation	p.Arg32His(p.R32H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216338
Start	24606731:24606731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613C>T
AA Mutation	p.Pro205Ser(p.P205S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216338
Start	24606704:24606704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640G>T
AA Mutation	p.Gly214Cys(p.G214C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GZMH

No Mutation Annotation!