Colon Cancer: Gene >> BDKRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96240962:96240962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199803197
CDS Mutation	c.634G>A
AA Mutation	p.Val212Ile(p.V212I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96241059:96241059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731C>T
AA Mutation	p.Thr244Met(p.T244M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96241209:96241209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201732624
CDS Mutation	c.881C>T
AA Mutation	p.Thr294Met(p.T294M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96240569:96240569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200683377
CDS Mutation	c.241G>A
AA Mutation	p.Val81Ile(p.V81I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96241360:96241360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032G>T
AA Mutation	p.Trp344Cys(p.W344C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96240924:96240924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596A>C
AA Mutation	p.Lys199Thr(p.K199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554311
Start	96240607:96240607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554311
Start	96241316:96241316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BDKRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96240713:96240713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>T
AA Mutation	p.Leu129Phe(p.L129F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96240953:96240953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625A>G
AA Mutation	p.Thr209Ala(p.T209A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000554311
Start	96237138:96237138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>A
AA Mutation	p.Leu11Met(p.L11M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554311
Start	96240691:96240691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745845591
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript