Colon Cancer: Gene >> MLX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246912
Start	42570143:42570143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800C>T
AA Mutation	p.Ala267Val(p.A267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246912
Start	42568938:42568938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433A>T
AA Mutation	p.Ile145Phe(p.I145F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246912
Start	42568536:42568536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.308G>A
AA Mutation	p.Ser103Asn(p.S103N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246912
Start	42568935:42568935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759737992
CDS Mutation	c.430G>A
AA Mutation	p.Ala144Thr(p.A144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MLX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246912
Start	42568935:42568935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759737992
CDS Mutation	c.430G>A
AA Mutation	p.Ala144Thr(p.A144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript