Primary Site >> Stomach Cancer

Gene >> EML4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318522
Start 42295492:42295492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1465C>T
AA Mutation p.Pro489Ser(p.P489S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318522
Start 42263239:42263239(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376838322
CDS Mutation c.574C>T
AA Mutation p.Arg192Cys(p.R192C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318522
Start 42263232:42263232(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.567T>A
AA Mutation p.Asp189Glu(p.D189E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000318522
Start 42280919:42280919(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.737A>G
AA Mutation p.Asn246Ser(p.N246S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000318522
Start 42261162:42261162(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs770453803
CDS Mutation c.387delA
AA Mutation p.Glu130ArgfsTer43(p.E130Rfs*43)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000318522
Start 42261161:42261161(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.379delG
AA Mutation p.Glu127LysfsTer46(p.E127Kfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript