Primary Site >> Stomach Cancer

Gene >> EFEMP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307998
Start 65870629:65870629(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766172211
CDS Mutation c.397G>T
AA Mutation p.Asp133Tyr(p.D133Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000307998
Start 65871157:65871157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.367G>C
AA Mutation p.Asp123His(p.D123H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000307998
Start 65870121:65870121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.607G>A
AA Mutation p.Asp203Asn(p.D203N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000307998
Start 65871268:65871268(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776088168
CDS Mutation c.256G>A
AA Mutation p.Ala86Thr(p.A86T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000307998
Start 65868337:65868337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.932A>G
AA Mutation p.Asp311Gly(p.D311G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000307998
Start 65869938:65869938(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758563195
CDS Mutation c.646C>T
AA Mutation p.Arg216Cys(p.R216C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000307998
Start 65870626:65870626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.400T>C
AA Mutation p.Cys134Arg(p.C134R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000307998
Start 65870230:65870230(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757273990
CDS Mutation c.498C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000307998
Start 65866924:65866924(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1326C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000307998
Start 65867030:65867030(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1220delG
AA Mutation p.Gly407AlafsTer14(p.G407Afs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000307998
Start 65869949:65869949(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.635delC
AA Mutation p.Pro212HisfsTer137(p.P212Hfs*137)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence inframe_deletion
Transcription ID ENST00000307998
Start 65869863:65869865(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.719_721delCCT
AA Mutation p.Ser240del(p.S240del)
Mutation Classification In_Frame_Del
Feature Type Transcript