Colon Cancer: Gene >> AIFM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307864
Start	70115046:70115046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151190502
CDS Mutation	c.844G>A
AA Mutation	p.Ala282Thr(p.A282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307864
Start	70117836:70117836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774916584
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Trp(p.R198W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307864
Start	70124013:70124013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764181244
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AIFM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307864
Start	70123443:70123443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>T
AA Mutation	p.Asp86Tyr(p.D86Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307864
Start	70123454:70123454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245T>C
AA Mutation	p.Val82Ala(p.V82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript