Primary Site >> Stomach Cancer

Gene >> MAP2K2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262948
Start 4099245:4099245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.875A>G
AA Mutation p.His292Arg(p.H292R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262948
Start 4117553:4117553(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121434498
CDS Mutation c.169T>G
AA Mutation p.Phe57Val(p.F57V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000262948
Start 4097282:4097282(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143275018
CDS Mutation c.981C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262948
Start 4099313:4099313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779598598
CDS Mutation c.807G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262948
Start 4099376:4099376(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.744G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000262948
Start 4117563:4117563(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.159G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000262948
Start 4117506:4117506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.216C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000262948
Start 4099314:4099314(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.806delC
AA Mutation p.Pro269ArgfsTer58(p.P269Rfs*58)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000262948
Start 4117627:4117628(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.94dupG
AA Mutation p.Ala32GlyfsTer16(p.A32Gfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript