Colon Cancer: Gene >> ERGIC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348547
Start	35548550:35548550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139314230
CDS Mutation	c.503G>A
AA Mutation	p.Arg168His(p.R168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348547
Start	35557500:35557500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201180063
CDS Mutation	c.1148C>T
AA Mutation	p.Thr383Met(p.T383M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348547
Start	35557019:35557019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926C>T
AA Mutation	p.Ala309Val(p.A309V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348547
Start	35556266:35556266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745424936
CDS Mutation	c.874G>A
AA Mutation	p.Gly292Arg(p.G292R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348547
Start	35542905:35542905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331G>T
AA Mutation	p.Asp111Tyr(p.D111Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348547
Start	35542530:35542530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ERGIC3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000348547
Start	35542393:35542393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159G>T
AA Mutation	p.Glu53Asp(p.E53D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript