Colon Cancer: Gene >> MSX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000239243
Start	174729216:174729216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000239243
Start	174729213:174729213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754536048
CDS Mutation	c.434C>T
AA Mutation	p.Pro145Leu(p.P145L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000239243
Start	174724876:174724876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>A
AA Mutation	p.Gly73Arg(p.G73R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239243
Start	174729370:174729370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150352201
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239243
Start	174724701:174724701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MSX2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239243
Start	174724698:174724698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766427771
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript