Colon Cancer: Gene >> NEK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169508259:169508259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749461218
CDS Mutation	c.1738C>T
AA Mutation	p.Arg580Cys(p.R580C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169537855:169537855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750593852
CDS Mutation	c.1619G>A
AA Mutation	p.Arg540Gln(p.R540Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169555747:169555747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771824152
CDS Mutation	c.1535C>T
AA Mutation	p.Ala512Val(p.A512V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169577046:169577046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>A
AA Mutation	p.Ser301Tyr(p.S301Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169400545:169400545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3606C>A
AA Mutation	p.Phe1202Leu(p.F1202L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169590732:169590732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390A>T
AA Mutation	p.Lys130Asn(p.K130N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169580871:169580871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839T>C
AA Mutation	p.Phe280Ser(p.F280S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000439128
Start	169555720:169555720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562G>A
AA Mutation	p.Arg521Lys(p.R521K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169477205:169477205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374639577
CDS Mutation	c.2269C>T
AA Mutation	p.Arg757Cys(p.R757C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169477204:169477204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757319297
CDS Mutation	c.2270G>A
AA Mutation	p.Arg757His(p.R757H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169477301:169477301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173G>T
AA Mutation	p.Asp725Tyr(p.D725Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169507086:169507086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1874G>A
AA Mutation	p.Arg625Gln(p.R625Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439128
Start	169400614:169400614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772515579
CDS Mutation	c.3537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439128
Start	169424634:169424634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190807750
CDS Mutation	c.3057G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439128
Start	169433595:169433595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765193688
CDS Mutation	c.2751C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439128
Start	169602595:169602595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439128
Start	169587565:169587565(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.600delA
AA Mutation	p.Lys200AsnfsTer9(p.K200Nfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439128
Start	169507729:169507729(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1813delA
AA Mutation	p.Ile605SerfsTer4(p.I605Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439128
Start	169576937:169576937(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1011delA
AA Mutation	p.Lys337AsnfsTer13(p.K337Nfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439128
Start	169507052:169507052(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775849720
CDS Mutation	c.1908delA
AA Mutation	p.Val637CysfsTer34(p.V637Cfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000439128
Start	169580890:169580890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820G>T
AA Mutation	p.Glu274Ter(p.E274*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000439128
Start	169602020:169602020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>T
AA Mutation	p.Glu68Ter(p.E68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NEK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169400545:169400545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3606C>A
AA Mutation	p.Phe1202Leu(p.F1202L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169590749:169590749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373C>A
AA Mutation	p.Leu125Ile(p.L125I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439128
Start	169507738:169507738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804C>A
AA Mutation	p.Arg602Ser(p.R602S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439128
Start	169424619:169424619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3072A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000439128
Start	169507099:169507099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1861G>T
AA Mutation	p.Glu621Ter(p.E621*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript