Colon Cancer: Gene >> GPC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133953163:133953163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>C
AA Mutation	p.Arg75Thr(p.R75T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133753868:133753868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.646A>G
AA Mutation	p.Met216Val(p.M216V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133985419:133985419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>C
AA Mutation	p.Val11Leu(p.V11L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133699918:133699918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1143A>T
AA Mutation	p.Glu381Asp(p.E381D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133536185:133536185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1682C>T
AA Mutation	p.Pro561Leu(p.P561L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133699931:133699931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130A>G
AA Mutation	p.His377Arg(p.H377R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370818
Start	133692428:133692428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000370818
Start	133753916:133753916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>T
AA Mutation	p.Gly200Ter(p.G200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GPC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133953061:133953061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761660909
CDS Mutation	c.326C>T
AA Mutation	p.Ala109Val(p.A109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370818
Start	133753798:133753798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716T>A
AA Mutation	p.Val239Glu(p.V239E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370818
Start	133661838:133661838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1305G>A
Mutation Classification	Silent
Feature Type	Transcript