Primary Site >> Stomach Cancer

Gene >> TLR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000308979
Start 38797186:38797186(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1646G>A
AA Mutation p.Gly549Asp(p.G549D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000308979
Start 38798615:38798615(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.217A>G
AA Mutation p.Ile73Val(p.I73V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000308979
Start 38797847:38797847(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.985A>G
AA Mutation p.Lys329Glu(p.K329E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000308979
Start 38797396:38797396(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1436C>A
AA Mutation p.Ser479Tyr(p.S479Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000308979
Start 38797718:38797718(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1114A>G
AA Mutation p.Thr372Ala(p.T372A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000308979
Start 38797866:38797866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.966C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000308979
Start 38798319:38798319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.513A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000308979
Start 38798433:38798434(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.398_399delAA
AA Mutation p.Lys133ArgfsTer22(p.K133Rfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000308979
Start 38796527:38796527(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2305delT
AA Mutation p.Trp769GlyfsTer4(p.W769Gfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript