Colon Cancer: Gene >> BDNF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356660
Start	27658164:27658164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>A
AA Mutation	p.Arg134His(p.R134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356660
Start	27658185:27658185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380G>A
AA Mutation	p.Arg127Gln(p.R127Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356660
Start	27658530:27658530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35A>G
AA Mutation	p.Tyr12Cys(p.Y12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356660
Start	27658186:27658186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379C>T
AA Mutation	p.Arg127Trp(p.R127W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356660
Start	27658300:27658300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BDNF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356660
Start	27658333:27658333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Trp(p.R78W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356660
Start	27658119:27658119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>T
AA Mutation	p.Thr149Met(p.T149M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript