Mutation

Primary Site >> Stomach Cancer

Gene >> MAP3K11

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65613317:65613317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440G>A
AA Mutation	p.Arg147His(p.R147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65598436:65598436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751204773
CDS Mutation	c.2399G>A
AA Mutation	p.Arg800Gln(p.R800Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65607994:65607994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997G>A
AA Mutation	p.Gly333Ser(p.G333S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65599550:65599550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754035122
CDS Mutation	c.2050G>A
AA Mutation	p.Ala684Thr(p.A684T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65606736:65606736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773390948
CDS Mutation	c.1558G>A
AA Mutation	p.Gly520Arg(p.G520R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65613506:65613506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>T
AA Mutation	p.Trp84Leu(p.W84L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65606709:65606709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585C>T
AA Mutation	p.Arg529Trp(p.R529W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65598414:65598414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765225812
CDS Mutation	c.2421G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65608330:65608330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61736581
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65613130:65613130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756251314
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65608031:65608031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766718638
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65598408:65598408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2427A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309100
Start	65608067:65608067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.924delT
AA Mutation	p.Phe308LeufsTer9(p.F308Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309100
Start	65598364:65598364(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2471delG
AA Mutation	p.Gly824AlafsTer123(p.G824Afs*123)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309100
Start	65599525:65599525(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2075delC
AA Mutation	p.Pro692LeufsTer255(p.P692Lfs*255)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript