Colon Cancer: Gene >> KLK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326003
Start	50858220:50858220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373661565
CDS Mutation	c.398C>T
AA Mutation	p.Thr133Met(p.T133M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000326003
Start	50856242:50856242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Ala17Thr(p.A17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326003
Start	50860053:50860053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372901531
CDS Mutation	c.712G>A
AA Mutation	p.Glu238Lys(p.E238K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326003
Start	50856343:50856343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144294681
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326003
Start	50858053:50858053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KLK3

Mutation ID	1
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000326003
Start	50858458:50858458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript