Colon Cancer: Gene >> LRAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336356
Start	154744532:154744532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206G>A
AA Mutation	p.Arg69His(p.R69H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336356
Start	154749108:154749108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665T>C
AA Mutation	p.Ile222Thr(p.I222T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336356
Start	154744477:154744477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LRAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336356
Start	154744552:154744552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226G>A
AA Mutation	p.Asp76Asn(p.D76N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript