Colon Cancer: Gene >> FARS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274680
Start	5368737:5368737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167A>C
AA Mutation	p.Lys56Thr(p.K56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274680
Start	5404653:5404653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>C
AA Mutation	p.Asp242His(p.D242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274680
Start	5545288:5545288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746837108
CDS Mutation	c.1013G>A
AA Mutation	p.Arg338His(p.R338H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274680
Start	5431061:5431061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>C
AA Mutation	p.Asp265His(p.D265H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274680
Start	5369037:5369037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146988468
CDS Mutation	c.467C>T
AA Mutation	p.Thr156Met(p.T156M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000274680
Start	5431118:5431118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>T
AA Mutation	p.Glu284Ter(p.E284*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274680
Start	5404616:5404617(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.694_695dupAC
AA Mutation	p.Met233ProfsTer5(p.M233Pfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FARS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274680
Start	5771340:5771340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145697325
CDS Mutation	c.1267C>T
AA Mutation	p.Arg423Trp(p.R423W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274680
Start	5404558:5404558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629A>C
AA Mutation	p.Lys210Thr(p.K210T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript