Colon Cancer: Gene >> PLAGL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354765
Start	143942598:143942598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753924230
CDS Mutation	c.218G>A
AA Mutation	p.Arg73Gln(p.R73Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354765
Start	143942490:143942490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326A>G
AA Mutation	p.His109Arg(p.H109R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354765
Start	143941494:143941494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1322C>A
AA Mutation	p.Pro441His(p.P441H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354765
Start	143942476:143942476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340G>T
AA Mutation	p.Ala114Ser(p.A114S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354765
Start	143942232:143942232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584G>A
AA Mutation	p.Arg195His(p.R195H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354765
Start	143942216:143942216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PLAGL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354765
Start	143942067:143942067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749A>G
AA Mutation	p.Asn250Ser(p.N250S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354765
Start	143948128:143948128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539999694
CDS Mutation	c.9G>A
Mutation Classification	Silent
Feature Type	Transcript