Colon Cancer: Gene >> CBFB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290858
Start	67082267:67082267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761036715
CDS Mutation	c.454G>A
AA Mutation	p.Glu152Lys(p.E152K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290858
Start	67082294:67082294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753789494
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Trp(p.R161W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290858
Start	67098725:67098725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542G>T
AA Mutation	p.Arg181Ile(p.R181I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CBFB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290858
Start	67066763:67066763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364A>C
AA Mutation	p.Met122Leu(p.M122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript