Primary Site >> Stomach Cancer

Gene >> MET

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397752
Start 116700043:116700043(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs35776110
CDS Mutation c.959C>T
AA Mutation p.Ala320Val(p.A320V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397752
Start 116700263:116700263(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1179T>A
AA Mutation p.Asn393Lys(p.N393K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397752
Start 116777427:116777427(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3298A>G
AA Mutation p.Asn1100Asp(p.N1100D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000397752
Start 116699225:116699225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.141C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000397752
Start 116699336:116699336(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.252C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000397752
Start 116699759:116699759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368249740
CDS Mutation c.675T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000397752
Start 116699102:116699102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.18G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000397752
Start 116796007:116796007(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4056G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000397752
Start 116757664:116757664(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373842614
CDS Mutation c.1992G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000397752
Start 116757452:116757452(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1878T>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000397752
Start 116782057:116782057(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3596delA
AA Mutation p.Lys1199SerfsTer49(p.K1199Sfs*49)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000397752
Start 116740963:116740963(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1639C>T
AA Mutation p.Arg547Ter(p.R547*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000397752
Start 116795908:116795908(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3957C>A
AA Mutation p.Cys1319Ter(p.C1319*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000397752
Start 116763123:116763124(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2443dupC
AA Mutation p.Leu815ProfsTer18(p.L815Pfs*18)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000397752
Start 116783302:116783302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3633-2A>G
Mutation Classification Splice_Site
Feature Type Transcript