Mutation

Primary Site >> Stomach Cancer

Gene >> MAP3K4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161048787:161048787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Gly172Glu(p.G172E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049942:161049942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1670C>T
AA Mutation	p.Ala557Val(p.A557V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049557:161049557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285A>T
AA Mutation	p.Ile429Phe(p.I429F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161101975:161101975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3758C>A
AA Mutation	p.Pro1253His(p.P1253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049364:161049364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092A>G
AA Mutation	p.Ile364Met(p.I364M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049645:161049645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549353618
CDS Mutation	c.1373C>T
AA Mutation	p.Thr458Met(p.T458M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161092023:161092023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3149T>G
AA Mutation	p.Val1050Gly(p.V1050G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049560:161049560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288C>A
AA Mutation	p.Pro430Thr(p.P430T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161092983:161092983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3275C>T
AA Mutation	p.Ala1092Val(p.A1092V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049388:161049388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116G>T
AA Mutation	p.Gln372His(p.Q372H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161108796:161108796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4173G>T
AA Mutation	p.Leu1391Phe(p.L1391F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161073517:161073517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002T>C
AA Mutation	p.Tyr668His(p.Y668H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161089356:161089356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2858C>T
AA Mutation	p.Ala953Val(p.A953V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161080986:161080986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2203G>A
AA Mutation	p.Glu735Lys(p.E735K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161106661:161106661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4004G>A
AA Mutation	p.Gly1335Asp(p.G1335D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049909:161049909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637T>G
AA Mutation	p.Leu546Arg(p.L546R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161091415:161091415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3010G>A
AA Mutation	p.Ala1004Thr(p.A1004T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161087814:161087814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779114335
CDS Mutation	c.2683G>A
AA Mutation	p.Val895Ile(p.V895I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161112718:161112718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4570C>T
AA Mutation	p.Arg1524Cys(p.R1524C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161049451:161049451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161049718:161049718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161080940:161080940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536943325
CDS Mutation	c.2157G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048744:161048744(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.479delA
AA Mutation	p.Asn160MetfsTer8(p.N160Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161034359:161034359(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.258delC
AA Mutation	p.Ser87AlafsTer6(p.S87Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161106561:161106561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3904C>T
AA Mutation	p.Arg1302Ter(p.R1302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161101986:161101986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3769C>T
AA Mutation	p.Arg1257Ter(p.R1257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048944:161048945(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.678dupT
AA Mutation	p.Glu227Ter(p.E227*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048743:161048744(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.479dupA
AA Mutation	p.Asn160LysfsTer27(p.N160Kfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript