Colon Cancer: Gene >> KLK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310157
Start	50967281:50967281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>T
AA Mutation	p.Asp29Tyr(p.D29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310157
Start	50959220:50959220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679T>C
AA Mutation	p.Tyr227His(p.Y227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310157
Start	50968086:50968086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19G>C
AA Mutation	p.Val7Leu(p.V7L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310157
Start	50967274:50967274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765571984
CDS Mutation	c.92C>T
AA Mutation	p.Thr31Ile(p.T31I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310157
Start	50963416:50963416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756725993
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Cys(p.R111C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310157
Start	50967291:50967291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KLK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310157
Start	50961862:50961862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464T>C
AA Mutation	p.Ile155Thr(p.I155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310157
Start	50963537:50963537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210C>A
Mutation Classification	Silent
Feature Type	Transcript