Primary Site >> Stomach Cancer

Gene >> TAS1R1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333172
Start 6576439:6576439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1285C>T
AA Mutation p.His429Tyr(p.H429Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333172
Start 6571070:6571070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.353T>C
AA Mutation p.Val118Ala(p.V118A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333172
Start 6574670:6574670(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs534950007
CDS Mutation c.538C>T
AA Mutation p.Arg180Trp(p.R180W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000333172
Start 6571186:6571186(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139619592
CDS Mutation c.469G>A
AA Mutation p.Ala157Thr(p.A157T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000333172
Start 6570949:6570949(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749567635
CDS Mutation c.232G>A
AA Mutation p.Ala78Thr(p.A78T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000333172
Start 6577026:6577026(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1550T>C
AA Mutation p.Phe517Ser(p.F517S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000333172
Start 6579320:6579320(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745625471
CDS Mutation c.2262G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000333172
Start 6577045:6577045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1569G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000333172
Start 6576416:6576416(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1265delT
AA Mutation p.Leu422TrpfsTer30(p.L422Wfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000333172
Start 6574892:6574892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.760G>T
AA Mutation p.Glu254Ter(p.E254*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript