Colon Cancer: Gene >> PDHB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302746
Start	58428155:58428155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959C>T
AA Mutation	p.Ala320Val(p.A320V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302746
Start	58430801:58430801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445G>A
AA Mutation	p.Gly149Ser(p.G149S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302746
Start	58429713:58429713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787T>C
AA Mutation	p.Cys263Arg(p.C263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302746
Start	58431924:58431924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Val53Ile(p.V53I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302746
Start	58428136:58428136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302746
Start	58428058:58428058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PDHB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302746
Start	58428172:58428172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148770511
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript