Colon Cancer: Gene >> MYL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279022
Start	36544904:36544904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20A>G
AA Mutation	p.Lys7Arg(p.K7R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279022
Start	36544901:36544901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17C>T
AA Mutation	p.Ala6Val(p.A6V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279022
Start	36548162:36548162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs7273824
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279022
Start	36544953:36544953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199568309
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MYL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279022
Start	36544924:36544924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40C>T
AA Mutation	p.Arg14Trp(p.R14W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279022
Start	36544953:36544953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199568309
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript