Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> WNK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93289151:93289151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4508G>T
AA Mutation	p.Arg1503Met(p.R1503M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93297978:93297978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5945G>A
AA Mutation	p.Arg1982His(p.R1982H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93297902:93297902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762379413
CDS Mutation	c.5869G>A
AA Mutation	p.Glu1957Lys(p.E1957K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93252931:93252931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553438989
CDS Mutation	c.1883C>T
AA Mutation	p.Ser628Leu(p.S628L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93264026:93264026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765314674
CDS Mutation	c.3689C>T
AA Mutation	p.Thr1230Met(p.T1230M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93292831:93292831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780729757
CDS Mutation	c.5477G>A
AA Mutation	p.Arg1826Gln(p.R1826Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93230941:93230941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908G>A
AA Mutation	p.Arg303Gln(p.R303Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93261856:93261856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3109G>A
AA Mutation	p.Ala1037Thr(p.A1037T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93292779:93292779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762615300
CDS Mutation	c.5425G>A
AA Mutation	p.Asp1809Asn(p.D1809N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93247646:93247646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139992553
CDS Mutation	c.1646C>T
AA Mutation	p.Ala549Val(p.A549V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93306786:93306786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6335T>C
AA Mutation	p.Leu2112Pro(p.L2112P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93239857:93239857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423G>A
AA Mutation	p.Ala475Thr(p.A475T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93288983:93288983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749370747
CDS Mutation	c.4340C>T
AA Mutation	p.Ala1447Val(p.A1447V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93292866:93292866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376742916
CDS Mutation	c.5512G>A
AA Mutation	p.Val1838Met(p.V1838M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93185521:93185521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592G>A
AA Mutation	p.Asp198Asn(p.D198N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93299211:93299211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746469152
CDS Mutation	c.6176C>T
AA Mutation	p.Ser2059Leu(p.S2059L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93230953:93230953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920A>C
AA Mutation	p.Lys307Thr(p.K307T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93292969:93292969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5615A>T
AA Mutation	p.Asp1872Val(p.D1872V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93292389:93292389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5129T>C
AA Mutation	p.Val1710Ala(p.V1710A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93234826:93234826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094C>T
AA Mutation	p.Ala365Val(p.A365V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93247603:93247603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603C>T
AA Mutation	p.Arg535Cys(p.R535C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93259550:93259550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531255333
CDS Mutation	c.3002G>A
AA Mutation	p.Arg1001His(p.R1001H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93247605:93247605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190904368
CDS Mutation	c.1605C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93289368:93289368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531755309
CDS Mutation	c.4725G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93239784:93239784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93289200:93289200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4557C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93230981:93230981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757165472
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93288930:93288930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4287T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93229860:93229860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745894034
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93289566:93289566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4923G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93185520:93185520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93308488:93308488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143815173
CDS Mutation	c.6531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93268058:93268058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3906G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93256968:93256968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377507851
CDS Mutation	c.2211G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93261903:93261903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540818950
CDS Mutation	c.3156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93292580:93292580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55812206
CDS Mutation	c.5226G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93289044:93289044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93268706:93268706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778896854
CDS Mutation	c.3993C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93252983:93252983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143979324
CDS Mutation	c.1935G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93289491:93289491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370214976
CDS Mutation	c.4848C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93234938:93234938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373701322
CDS Mutation	c.1206G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297954
Start	93288908:93288908(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4269delC
AA Mutation	p.Ser1424ProfsTer5(p.S1424Pfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297954
Start	93297965:93297965(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5937delC
AA Mutation	p.Thr1980LeufsTer12(p.T1980Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297954
Start	93317925:93317925(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6798delC
AA Mutation	p.Thr2267ProfsTer49(p.T2267Pfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297954
Start	93317924:93317925(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs778478950
CDS Mutation	c.6798dupC
AA Mutation	p.Thr2267HisfsTer48(p.T2267Hfs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000297954
Start	93268066:93268066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3913+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000297954
Start	93229694:93229694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WNK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297954
Start	93262683:93262683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3374A>C
AA Mutation	p.Gln1125Pro(p.Q1125P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93239763:93239763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297954
Start	93292577:93292577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5223G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000297954
Start	93288791:93288791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4148C>A
AA Mutation	p.Ser1383Ter(p.S1383*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript