Colon Cancer: Gene >> CDCP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45093406:45093406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Pro500Ser(p.P500S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45118534:45118534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170A>G
AA Mutation	p.Tyr57Cys(p.Y57C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45095422:45095422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171T>G
AA Mutation	p.Ser391Ala(p.S391A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45085937:45085937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764842004
CDS Mutation	c.2212G>A
AA Mutation	p.Glu738Lys(p.E738K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45093483:45093483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1421A>C
AA Mutation	p.Lys474Thr(p.K474T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45118603:45118603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.101T>C
AA Mutation	p.Leu34Pro(p.L34P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45085862:45085862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758096347
CDS Mutation	c.2287C>T
AA Mutation	p.Arg763Trp(p.R763W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296129
Start	45091357:45091357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370889670
CDS Mutation	c.1809C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296129
Start	45095540:45095540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296129
Start	45089092:45089092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2043G>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDCP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45085919:45085919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2230G>C
AA Mutation	p.Gly744Arg(p.G744R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296129
Start	45112260:45112260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478A>G
AA Mutation	p.Thr160Ala(p.T160A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript