Colon Cancer: Gene >> MYL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110913118:110913118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141878747
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110919123:110919123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74A>G
AA Mutation	p.Gln25Arg(p.Q25R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110913101:110913101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397G>A
AA Mutation	p.Glu133Lys(p.E133K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228841
Start	110911158:110911158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MYL2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228841
Start	110915758:110915758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript