Colon Cancer: Gene >> CDC14A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100424280:100424280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368A>C
AA Mutation	p.Asn123Thr(p.N123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100462665:100462665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371468460
CDS Mutation	c.622G>A
AA Mutation	p.Ala208Thr(p.A208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100494901:100494901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221G>T
AA Mutation	p.Gln407His(p.Q407H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100468012:100468012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895T>C
AA Mutation	p.Phe299Leu(p.F299L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100455445:100455445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560A>C
AA Mutation	p.Lys187Thr(p.K187T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100352973:100352973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19G>A
AA Mutation	p.Glu7Lys(p.E7K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100462693:100462693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650A>C
AA Mutation	p.Lys217Thr(p.K217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336454
Start	100390749:100390749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336454
Start	100498190:100498190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756072930
CDS Mutation	c.1404G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336454
Start	100442949:100442949(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.477delT
AA Mutation	p.Phe159LeufsTer31(p.F159Lfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336454
Start	100424281:100424281(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773911500
CDS Mutation	c.375delC
AA Mutation	p.Tyr126IlefsTer64(p.Y126Ifs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336454
Start	100499154:100499154(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1652delC
AA Mutation	p.Pro551GlnfsTer30(p.P551Qfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336454
Start	100499163:100499163(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1660delC
AA Mutation	p.His554ThrfsTer27(p.H554Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336454
Start	100424280:100424281(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.375dupC
AA Mutation	p.Tyr126LeufsTer35(p.Y126Lfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDC14A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100468051:100468051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148737918
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Trp(p.R312W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100499221:100499221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714C>A
AA Mutation	p.Leu572Ile(p.L572I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100353787:100353787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75G>T
AA Mutation	p.Arg25Ser(p.R25S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100424261:100424261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Ala117Thr(p.A117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336454
Start	100462704:100462704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661G>A
AA Mutation	p.Val221Met(p.V221M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336454
Start	100455488:100455488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336454
Start	100424280:100424281(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.375dupC
AA Mutation	p.Tyr126LeufsTer35(p.Y126Lfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript