Colon Cancer: Gene >> NFYA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341376
Start	41094441:41094441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Cys(p.R312C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341376
Start	41084088:41084088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205C>A
AA Mutation	p.Leu69Ile(p.L69I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341376
Start	41092919:41092919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722C>A
AA Mutation	p.Pro241His(p.P241H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341376
Start	41080864:41080864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138225735
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NFYA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341376
Start	41094432:41094432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>A
AA Mutation	p.Ala309Thr(p.A309T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341376
Start	41091615:41091615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635C>G
AA Mutation	p.Thr212Arg(p.T212R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript