Colon Cancer: Gene >> PDHX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227868
Start	34994945:34994945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371811647
CDS Mutation	c.1279G>A
AA Mutation	p.Glu427Lys(p.E427K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227868
Start	34916663:34916663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>G
AA Mutation	p.Ala3Gly(p.A3G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227868
Start	34995093:34995093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1427G>A
AA Mutation	p.Arg476Gln(p.R476Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227868
Start	34995057:34995057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760454961
CDS Mutation	c.1391G>A
AA Mutation	p.Arg464His(p.R464H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000227868
Start	34966767:34966767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768910663
CDS Mutation	c.769C>T
AA Mutation	p.Arg257Trp(p.R257W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227868
Start	34916766:34916766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PDHX

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227868
Start	34978155:34978155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.996C>A
Mutation Classification	Silent
Feature Type	Transcript