Colon Cancer: Gene >> KLK13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000595793
Start	51058633:51058633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372211156
CDS Mutation	c.550C>T
AA Mutation	p.Arg184Cys(p.R184C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000595793
Start	51060500:51060500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200725984
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Trp(p.R58W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000595793
Start	51058636:51058636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.547C>T
AA Mutation	p.Leu183Phe(p.L183F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000595793
Start	51058614:51058614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142773664
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000595793
Start	51059851:51059851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>A
AA Mutation	p.Gly161Asp(p.G161D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000595793
Start	51059968:51059968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365A>G
AA Mutation	p.Asp122Gly(p.D122G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595793
Start	51060501:51060501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000595793
Start	51056762:51056762(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.659delG
AA Mutation	p.Gly220AlafsTer54(p.G220Afs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KLK13

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595793
Start	51056728:51056728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765329818
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000595793
Start	51056634:51056634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536078012
CDS Mutation	c.787C>T
AA Mutation	p.Arg263Ter(p.R263*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript