Colon Cancer: Gene >> APCS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255040
Start	159588349:159588349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761743822
CDS Mutation	c.313G>A
AA Mutation	p.Glu105Lys(p.E105K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255040
Start	159588617:159588617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581G>T
AA Mutation	p.Gly194Val(p.G194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255040
Start	159588164:159588164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128C>T
AA Mutation	p.Thr43Ile(p.T43I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255040
Start	159588448:159588448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000255040
Start	159588451:159588451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415C>T
AA Mutation	p.Arg139Ter(p.R139*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255040
Start	159588520:159588521(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.484_485insGCACAGAGTCCCACATGTAC
AA Mutation	p.Lys162SerfsTer53(p.K162Sfs*53)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> APCS

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255040
Start	159588222:159588222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript