Primary Site >> Stomach Cancer

Gene >> TLE1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000376499
Start 81611858:81611858(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs556195256
CDS Mutation c.1165G>A
AA Mutation p.Ala389Thr(p.A389T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000376499
Start 81654002:81654002(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.269C>T
AA Mutation p.Ala90Val(p.A90V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000376499
Start 81584280:81584280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2231G>A
AA Mutation p.Ser744Asn(p.S744N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000376499
Start 81620482:81620482(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.670A>C
AA Mutation p.Ile224Leu(p.I224L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000376499
Start 81615992:81615992(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.908A>G
AA Mutation p.Glu303Gly(p.E303G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000376499
Start 81593105:81593105(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1501A>G
AA Mutation p.Thr501Ala(p.T501A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000376499
Start 81590900:81590900(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764412759
CDS Mutation c.1734C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000376499
Start 81611892:81611892(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371977486
CDS Mutation c.1131C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000376499
Start 81611808:81611808(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756514936
CDS Mutation c.1215C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000376499
Start 81610277:81610277(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1274delC
AA Mutation p.Pro425LeufsTer3(p.P425Lfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000376499
Start 81593217:81593217(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1389delC
AA Mutation p.Asp464ThrfsTer27(p.D464Tfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000376499
Start 81584232:81584233(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2278dupG
AA Mutation p.Asp760GlyfsTer8(p.D760Gfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence inframe_deletion
Transcription ID ENST00000376499
Start 81587693:81587695(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1963_1965delGAC
AA Mutation p.Asp655del(p.D655del)
Mutation Classification In_Frame_Del
Feature Type Transcript