Colon Cancer: Gene >> CD2AP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359314
Start	47533687:47533687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371293071
CDS Mutation	c.251G>A
AA Mutation	p.Arg84Gln(p.R84Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359314
Start	47544706:47544706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420G>T
AA Mutation	p.Glu140Asp(p.E140D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359314
Start	47503337:47503337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559978848
CDS Mutation	c.62G>A
AA Mutation	p.Arg21Gln(p.R21Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359314
Start	47595905:47595905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153C>G
AA Mutation	p.Pro385Ala(p.P385A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359314
Start	47582024:47582024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067C>A
AA Mutation	p.Ala356Asp(p.A356D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359314
Start	47595996:47595996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244A>G
AA Mutation	p.Lys415Arg(p.K415R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359314
Start	47574098:47574098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359314
Start	47577085:47577085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD2AP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359314
Start	47576594:47576594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800A>T
AA Mutation	p.Lys267Ile(p.K267I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359314
Start	47606170:47606170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423G>A
AA Mutation	p.Val475Ile(p.V475I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000359314
Start	47580863:47580863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript