Colon Cancer: Gene >> NDUFA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266544
Start	4686983:4686983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>T
AA Mutation	p.Asp337Tyr(p.D337Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000266544
Start	4654827:4654827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767462328
CDS Mutation	c.223C>T
AA Mutation	p.Arg75Cys(p.R75C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266544
Start	4657812:4657812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383A>G
AA Mutation	p.Asn128Ser(p.N128S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266544
Start	4659044:4659044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419A>G
AA Mutation	p.Asp140Gly(p.D140G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266544
Start	4657757:4657757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772426441
CDS Mutation	c.328G>A
AA Mutation	p.Ala110Thr(p.A110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266544
Start	4687093:4687093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119G>T
AA Mutation	p.Lys373Asn(p.K373N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266544
Start	4649143:4649143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17A>G
AA Mutation	p.Gln6Arg(p.Q6R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NDUFA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266544
Start	4662608:4662608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628G>A
AA Mutation	p.Glu210Lys(p.E210K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript