Colon Cancer: Gene >> PLAGL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246229
Start	32201989:32201989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190G>C
AA Mutation	p.Glu64Gln(p.E64Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246229
Start	32196880:32196880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760161049
CDS Mutation	c.1063C>T
AA Mutation	p.Pro355Ser(p.P355S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246229
Start	32197010:32197010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246229
Start	32202149:32202149(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.30delC
AA Mutation	p.Trp11GlyfsTer15(p.W11Gfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246229
Start	32202165:32202165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.14delT
AA Mutation	p.Phe5SerfsTer21(p.F5Sfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLAGL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246229
Start	32201932:32201932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247T>C
AA Mutation	p.Tyr83His(p.Y83H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246229
Start	32202149:32202149(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.30delC
AA Mutation	p.Trp11GlyfsTer15(p.W11Gfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript