Colon Cancer: Gene >> APOL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397278
Start	36265413:36265413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183714534
CDS Mutation	c.577G>A
AA Mutation	p.Gly193Ser(p.G193S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397278
Start	36265207:36265207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773763181
CDS Mutation	c.371T>C
AA Mutation	p.Met124Thr(p.M124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397278
Start	36265843:36265843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553515630
CDS Mutation	c.1007C>T
AA Mutation	p.Thr336Met(p.T336M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397278
Start	36266018:36266018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185040686
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> APOL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397278
Start	36265504:36265504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668T>C
AA Mutation	p.Ile223Thr(p.I223T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397278
Start	36265247:36265247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411A>T
AA Mutation	p.Arg137Ser(p.R137S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript