Primary Site >> Stomach Cancer

Gene >> ARNTL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000403290
Start 13358463:13358463(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.251G>A
AA Mutation p.Arg84His(p.R84H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000403290
Start 13366782:13366782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.670A>T
AA Mutation p.Thr224Ser(p.T224S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000403290
Start 13372193:13372193(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.851G>T
AA Mutation p.Ser284Ile(p.S284I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000403290
Start 13372288:13372288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.946G>A
AA Mutation p.Ala316Thr(p.A316T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000403290
Start 13378388:13378388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1466G>A
AA Mutation p.Arg489Gln(p.R489Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000403290
Start 13366700:13366700(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767607113
CDS Mutation c.588G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000403290
Start 13372332:13372332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144535593
CDS Mutation c.990C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000403290
Start 13360385:13360385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.420T>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000403290
Start 13381176:13381176(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199959315
CDS Mutation c.1539G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000403290
Start 13376690:13376690(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1381delC
AA Mutation p.His461ThrfsTer35(p.H461Tfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000403290
Start 13372249:13372249(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.907G>T
AA Mutation p.Glu303Ter(p.E303*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000403290
Start 13358590:13358591(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.378_379insAAAGATGACAAAAATAAAT
AA Mutation p.Gly127LysfsTer26(p.G127Kfs*26)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000403290
Start 13372393:13372394(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1056dupT
AA Mutation p.Val353CysfsTer23(p.V353Cfs*23)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript