Colon Cancer: Gene >> MEST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223215
Start	130495405:130495405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781957359
CDS Mutation	c.64G>A
AA Mutation	p.Val22Met(p.V22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223215
Start	130498239:130498239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440A>T
AA Mutation	p.Asp147Val(p.D147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223215
Start	130497958:130497958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>T
AA Mutation	p.Arg95Met(p.R95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223215
Start	130504952:130504952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756420254
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Trp(p.R302W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223215
Start	130500842:130500842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701A>G
AA Mutation	p.Asp234Gly(p.D234G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000223215
Start	130500501:130500501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616C>T
AA Mutation	p.Arg206Ter(p.R206*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MEST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223215
Start	130495508:130495508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561353737
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223215
Start	130499888:130499888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549G>T
AA Mutation	p.Glu183Asp(p.E183D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript