Colon Cancer: Gene >> CDK14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	91045900:91045900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045C>A
AA Mutation	p.Leu349Ile(p.L349I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	90917646:90917646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758302947
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Cys(p.R250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	90747745:90747745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434C>G
AA Mutation	p.Ser145Cys(p.S145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	90899333:90899333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682C>A
AA Mutation	p.Leu228Met(p.L228M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	90984216:90984216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016A>G
AA Mutation	p.Gln339Arg(p.Q339R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380050
Start	90726567:90726567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124A>T
AA Mutation	p.Ile42Leu(p.I42L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	91112561:91112561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112642464
CDS Mutation	c.1174G>A
AA Mutation	p.Ala392Thr(p.A392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	90899303:90899303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652T>C
AA Mutation	p.Cys218Arg(p.C218R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380050
Start	90917666:90917666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380050
Start	90747686:90747686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380050
Start	90790606:90790606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380050
Start	90917699:90917699(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.805delG
AA Mutation	p.Glu269SerfsTer2(p.E269Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380050
Start	90899327:90899327(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.681delG
AA Mutation	p.Leu228CysfsTer6(p.L228Cfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000380050
Start	90790622:90790622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.514G>T
AA Mutation	p.Glu172Ter(p.E172*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000380050
Start	90984230:90984230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030C>T
AA Mutation	p.Arg344Ter(p.R344*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000380050
Start	90984241:90984242(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1041_1041+1insCTTA
AA Mutation	p.Val348LeufsTer8(p.V348Lfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000380050
Start	90790616:90790618(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773042961
CDS Mutation	c.515_517delAAG
AA Mutation	p.Glu172del(p.E172del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDK14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380050
Start	90863259:90863259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629T>C
AA Mutation	p.Phe210Ser(p.F210S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380050
Start	90955740:90955740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript