Primary Site >> Stomach Cancer

Gene >> ELF3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359651
Start 202012145:202012145(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.352G>T
AA Mutation p.Gly118Trp(p.G118W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359651
Start 202015259:202015259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1052T>C
AA Mutation p.Val351Ala(p.V351A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359651
Start 202015238:202015238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1031G>T
AA Mutation p.Arg344Leu(p.R344L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359651
Start 202015211:202015211(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1004A>G
AA Mutation p.Tyr335Cys(p.Y335C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359651
Start 202014018:202014018(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.995C>T
AA Mutation p.Ala332Val(p.A332V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359651
Start 202013930:202013930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.907T>A
AA Mutation p.Phe303Ile(p.F303I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359651
Start 202012104:202012104(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs58166377
CDS Mutation c.311A>G
AA Mutation p.Asn104Ser(p.N104S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000359651
Start 202011165:202011165(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.33delT
AA Mutation p.Phe11LeufsTer32(p.F11Lfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000359651
Start 202013262:202013263(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.770dupA
AA Mutation p.Tyr257Ter(p.Y257*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000359651
Start 202012407:202012408(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.451dupC
AA Mutation p.Gln151ProfsTer10(p.Q151Pfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000359651
Start 202013838:202013839(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.820_823dupCACC
AA Mutation p.Leu275ProfsTer27(p.L275Pfs*27)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000359651
Start 202012983:202012984(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.636_640dupCGGTG
AA Mutation p.Gly214AlafsTer42(p.G214Afs*42)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000359651
Start 202012139:202012140(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.349_350dupCT
AA Mutation p.Gly118TrpfsTer38(p.G118Wfs*38)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 14
Mutation Consequence splice_donor_variant;coding_sequence_variant
Transcription ID ENST00000359651
Start 202012435:202012437(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.478+1_478+3delGTG
Mutation Classification Splice_Site
Feature Type Transcript
ID 15
Mutation Consequence inframe_deletion
Transcription ID ENST00000359651
Start 202012365:202012373(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.410_418delGTTGGATCA
AA Mutation p.Ser137_Ile139del(p.S137_I139del)
Mutation Classification In_Frame_Del
Feature Type Transcript