Mutation

Primary Site >> Stomach Cancer

Gene >> WNK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	884199:884199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3800G>T
AA Mutation	p.Arg1267Leu(p.R1267L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	830095:830095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246G>A
AA Mutation	p.Ala416Thr(p.A416T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896132:896132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5645C>T
AA Mutation	p.Ser1882Phe(p.S1882F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	885137:885137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535135770
CDS Mutation	c.4333A>G
AA Mutation	p.Thr1445Ala(p.T1445A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	886032:886032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5228C>T
AA Mutation	p.Ser1743Leu(p.S1743L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	753750:753750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185A>G
AA Mutation	p.Asp62Gly(p.D62G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	859322:859322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478A>G
AA Mutation	p.Asp493Gly(p.D493G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	885508:885508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4704T>A
AA Mutation	p.His1568Gln(p.H1568Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	897511:897511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200315094
CDS Mutation	c.6278G>A
AA Mutation	p.Arg2093His(p.R2093H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896357:896357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs36083875
CDS Mutation	c.5870G>A
AA Mutation	p.Arg1957His(p.R1957H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896261:896261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5774C>T
AA Mutation	p.Ala1925Val(p.A1925V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	880893:880893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3005A>G
AA Mutation	p.Asn1002Ser(p.N1002S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896403:896403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5916A>T
AA Mutation	p.Lys1972Asn(p.K1972N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	897522:897522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6289G>A
AA Mutation	p.Glu2097Lys(p.E2097K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	885530:885530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4726A>G
AA Mutation	p.Ile1576Val(p.I1576V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	859274:859274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430C>T
AA Mutation	p.Ala477Val(p.A477V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896213:896213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548442202
CDS Mutation	c.5726C>T
AA Mutation	p.Pro1909Leu(p.P1909L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	813746:813746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864A>T
AA Mutation	p.Glu288Asp(p.E288D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	879648:879648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2449C>A
AA Mutation	p.Pro817Thr(p.P817T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	896689:896689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6202G>A
AA Mutation	p.Glu2068Lys(p.E2068K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000315939
Start	857228:857228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379T>C
AA Mutation	p.Ile460Thr(p.I460T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	827177:827177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	885055:885055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766701999
CDS Mutation	c.4251A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	827255:827255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	894632:894632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5580T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	900519:900519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6492G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	883809:883809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147752204
CDS Mutation	c.3699G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	830040:830040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315939
Start	879851:879851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2652G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315939
Start	859331:859331(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1492delA
AA Mutation	p.Ile498Ter(p.I498*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315939
Start	908762:908762(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7124delC
AA Mutation	p.Pro2375GlnfsTer15(p.P2375Qfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000315939
Start	883515:883515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3610C>T
AA Mutation	p.Gln1204Ter(p.Q1204*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315939
Start	885736:885737(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4935dupA
AA Mutation	p.Ala1646SerfsTer5(p.A1646Sfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315939
Start	879757:879758(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2558_2559insAG
AA Mutation	p.Ala854GlyfsTer51(p.A854Gfs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315939
Start	908761:908762(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.7124dupC
AA Mutation	p.Gly2376ArgfsTer16(p.G2376Rfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript