Colon Cancer: Gene >> PYGO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368457
Start	154958799:154958799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201G>A
AA Mutation	p.Val401Met(p.V401M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368457
Start	154958907:154958907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>A
AA Mutation	p.Ala365Thr(p.A365T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368457
Start	154959108:154959108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757615029
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Trp(p.R298W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368457
Start	154959121:154959121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750392591
CDS Mutation	c.879G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368457
Start	154959019:154959019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368457
Start	154959424:154959424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368457
Start	154959595:154959595(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.405delC
AA Mutation	p.Phe136SerfsTer25(p.F136Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368457
Start	154959220:154959220(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.780delG
AA Mutation	p.Lys261SerfsTer3(p.K261Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368457
Start	154959552:154959552(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.448delC
AA Mutation	p.Gln150ArgfsTer11(p.Q150Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368457
Start	154959674:154959674(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.326delG
AA Mutation	p.Gly109AlafsTer52(p.G109Afs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000368457
Start	154959360:154959360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Ter(p.R214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368457
Start	154959551:154959552(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs748504064
CDS Mutation	c.448dupC
AA Mutation	p.Gln150ProfsTer27(p.Q150Pfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PYGO2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368457
Start	154959478:154959478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773146776
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript