Colon Cancer: Gene >> SMUG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337581
Start	54183745:54183745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371582477
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Cys(p.R66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337581
Start	54183792:54183792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149C>A
AA Mutation	p.Pro50His(p.P50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337581
Start	54182475:54182475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434T>C
AA Mutation	p.Phe145Ser(p.F145S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	start_lost
Transcription ID	ENST00000337581
Start	54183939:54183939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747175374
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SMUG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337581
Start	54183831:54183831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376491349
CDS Mutation	c.110G>A
AA Mutation	p.Arg37Gln(p.R37Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337581
Start	54183729:54183729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549646851
CDS Mutation	c.212G>A
AA Mutation	p.Arg71His(p.R71H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript