Colon Cancer: Gene >> CD46

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358170
Start	207785677:207785677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1122G>T
AA Mutation	p.Lys374Asn(p.K374N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358170
Start	207761327:207761327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747504551
CDS Mutation	c.554A>G
AA Mutation	p.Asp185Gly(p.D185G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358170
Start	207759671:207759671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Cys141Tyr(p.C141Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358170
Start	207770342:207770342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968C>A
AA Mutation	p.Pro323His(p.P323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358170
Start	207783314:207783314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1011A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD46

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358170
Start	207767071:207767071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732A>C
AA Mutation	p.Lys244Asn(p.K244N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358170
Start	207785650:207785650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript