Colon Cancer: Gene >> BDKRB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216629
Start	96264251:96264251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>C
AA Mutation	p.Ile190Thr(p.I190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216629
Start	96264209:96264209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145002930
CDS Mutation	c.527G>A
AA Mutation	p.Arg176Gln(p.R176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216629
Start	96264737:96264737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376526644
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352Gln(p.R352Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216629
Start	96264684:96264684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002T>G
AA Mutation	p.Ser334Arg(p.S334R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216629
Start	96263802:96263802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216629
Start	96264732:96264732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000216629
Start	96264208:96264208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200342765
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Ter(p.R176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BDKRB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216629
Start	96264553:96264553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>T
AA Mutation	p.Asp291Tyr(p.D291Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000216629
Start	96264715:96264715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033G>T
AA Mutation	p.Glu345Ter(p.E345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript