Colon Cancer: Gene >> KLK8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000600767
Start	50996187:50996187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>A
AA Mutation	p.Asp219Asn(p.D219N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000600767
Start	50997847:50997847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531A>C
AA Mutation	p.Lys177Asn(p.K177N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000600767
Start	51000070:51000070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419G>A
AA Mutation	p.Ser140Asn(p.S140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000600767
Start	51000222:51000222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267G>T
AA Mutation	p.Gln89His(p.Q89H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000600767
Start	51001109:51001109(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.59delG
AA Mutation	p.Gly20GlufsTer44(p.G20Efs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000600767
Start	50996215:50996215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KLK8

No Mutation Annotation!