Mutation

Primary Site >> Stomach Cancer

Gene >> MAP2K7

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397979
Start	7912150:7912150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081C>T
AA Mutation	p.Leu361Phe(p.L361F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911080:7911080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776T>C
AA Mutation	p.Leu259Pro(p.L259P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911253:7911253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859G>A
AA Mutation	p.Glu287Lys(p.E287K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910462:7910462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Cys(p.R153C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910702:7910702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574G>A
AA Mutation	p.Val192Ile(p.V192I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910320:7910320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755099146
CDS Mutation	c.394G>A
AA Mutation	p.Gly132Ser(p.G132S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911562:7911562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063T>C
AA Mutation	p.Ser355Pro(p.S355P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910311:7910311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>A
AA Mutation	p.Gly129Ser(p.G129S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910463:7910463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911316:7911316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922C>A
AA Mutation	p.Leu308Met(p.L308M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910735:7910735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607G>A
AA Mutation	p.Ala203Thr(p.A203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911298:7911298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Trp(p.R302W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7912316:7912316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759229847
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7912304:7912304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1133G>T
AA Mutation	p.Ser378Ile(p.S378I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910489:7910489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911131:7911131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827G>A
AA Mutation	p.Arg276Gln(p.R276Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910468:7910468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>A
AA Mutation	p.Gly155Arg(p.G155R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911304:7911304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769642939
CDS Mutation	c.910G>A
AA Mutation	p.Asp304Asn(p.D304N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7912156:7912156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087A>G
AA Mutation	p.Lys363Glu(p.K363E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911128:7911128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824C>T
AA Mutation	p.Thr275Met(p.T275M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911479:7911479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980C>T
AA Mutation	p.Thr327Met(p.T327M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911031:7911031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Asp243Asn(p.D243N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7912315:7912315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774212941
CDS Mutation	c.1144C>T
AA Mutation	p.Arg382Cys(p.R382C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911085:7911085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Asp261Asn(p.D261N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910490:7910490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485G>A
AA Mutation	p.Arg162His(p.R162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397979
Start	7910121:7910121(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.329delG
AA Mutation	p.Gly110AlafsTer62(p.G110Afs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397979
Start	7911264:7911264(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.875delC
AA Mutation	p.Pro292GlnfsTer119(p.P292Qfs*119)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000397979
Start	7911439:7911439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.940G>T
AA Mutation	p.Glu314Ter(p.E314*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000397979
Start	7911249:7911249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.856-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000397979
Start	7910375:7910375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	31
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000397979
Start	7912186:7912188(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1117_1119delAAG
AA Mutation	p.Lys373del(p.K373del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript