Colon Cancer: Gene >> CDC14B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375241
Start	96564786:96564786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318G>T
AA Mutation	p.Lys106Asn(p.K106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375241
Start	96565432:96565432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212T>C
AA Mutation	p.Val71Ala(p.V71A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375241
Start	96533966:96533966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907T>C
AA Mutation	p.Cys303Arg(p.C303R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000375241
Start	96503788:96503788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462C>A
AA Mutation	p.Leu488Ile(p.L488I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375241
Start	96534487:96534487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683G>A
AA Mutation	p.Cys228Tyr(p.C228Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375241
Start	96523351:96523351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1155A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375241
Start	96523267:96523267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375241
Start	96523709:96523709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367899199
CDS Mutation	c.963G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDC14B

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000375241
Start	96565481:96565481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373460925
CDS Mutation	c.163C>T
AA Mutation	p.Arg55Cys(p.R55C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375241
Start	96523383:96523383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773237782
CDS Mutation	c.1123C>T
AA Mutation	p.Arg375Cys(p.R375C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript