Colon Cancer: Gene >> KLK11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000594768
Start	51024732:51024732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199T>C
AA Mutation	p.Trp67Arg(p.W67R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000594768
Start	51024248:51024248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140954965
CDS Mutation	c.356G>A
AA Mutation	p.Arg119Gln(p.R119Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000594768
Start	51022624:51022624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759848513
CDS Mutation	c.770C>T
AA Mutation	p.Ala257Val(p.A257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000594768
Start	51024638:51024638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200477811
CDS Mutation	c.293C>T
AA Mutation	p.Pro98Leu(p.P98L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594768
Start	51023203:51023203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148855454
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000594768
Start	51022545:51022545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594768
Start	51024715:51024715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765126785
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000594768
Start	51022684:51022684(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.710delG
AA Mutation	p.Gly237AlafsTer43(p.G237Afs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KLK11

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594768
Start	51022629:51022629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542875015
CDS Mutation	c.765G>A
Mutation Classification	Silent
Feature Type	Transcript