Colon Cancer: Gene >> NEK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52752164:52752164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770168568
CDS Mutation	c.1136G>A
AA Mutation	p.Ser379Asn(p.S379N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52743419:52743419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1937G>T
AA Mutation	p.Gly646Val(p.G646V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52766212:52766212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524C>A
AA Mutation	p.Pro175His(p.P175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52760895:52760895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863C>G
AA Mutation	p.Ser288Cys(p.S288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52711859:52711859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141150064
CDS Mutation	c.2444G>A
AA Mutation	p.Arg815Gln(p.R815Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52739500:52739500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760299908
CDS Mutation	c.2228G>A
AA Mutation	p.Arg743Gln(p.R743Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52711784:52711784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2519A>T
AA Mutation	p.Asn840Ile(p.N840I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52746801:52746801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750998173
CDS Mutation	c.1610G>A
AA Mutation	p.Arg537Gln(p.R537Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52768591:52768591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107A>C
AA Mutation	p.Lys36Thr(p.K36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000233027
Start	52763472:52763472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819G>T
AA Mutation	p.Lys273Asn(p.K273N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52711815:52711815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56168225
CDS Mutation	c.2488C>T
AA Mutation	p.Arg830Cys(p.R830C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233027
Start	52743418:52743418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1938A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233027
Start	52752181:52752181(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1119delA
AA Mutation	p.Arg375GlyfsTer4(p.R375Gfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233027
Start	52711797:52711798(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2505dupT
AA Mutation	p.Glu836Ter(p.E836*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NEK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52765916:52765916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637T>C
AA Mutation	p.Ser213Pro(p.S213P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233027
Start	52766351:52766351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>A
AA Mutation	p.His129Asn(p.H129N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript