Colon Cancer: Gene >> SAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379270
Start	23783364:23783364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13G>A
AA Mutation	p.Val5Met(p.V5M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379270
Start	23785789:23785789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449G>T
AA Mutation	p.Ser150Ile(p.S150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379270
Start	23783704:23783704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.117delA
AA Mutation	p.Asp40IlefsTer3(p.D40Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000379270
Start	23783685:23783685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94G>T
AA Mutation	p.Glu32Ter(p.E32*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379270
Start	23785702:23785702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Arg121His(p.R121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript