Primary Site >> Stomach Cancer

Gene >> CLOCK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55450115:55450115(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1324C>T
AA Mutation p.His442Tyr(p.H442Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55479646:55479646(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.101C>T
AA Mutation p.Ala34Val(p.A34V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55478883:55478883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.188G>A
AA Mutation p.Gly63Asp(p.G63D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55459252:55459252(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.569A>G
AA Mutation p.Gln190Arg(p.Q190R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55479694:55479694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.53A>C
AA Mutation p.Asp18Ala(p.D18A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55438303:55438303(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2340G>T
AA Mutation p.Gln780His(p.Q780H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55478935:55478935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.136C>T
AA Mutation p.Arg46Cys(p.R46C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000309964
Start 55444737:55444737(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1588T>G
AA Mutation p.Leu530Val(p.L530V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000309964
Start 55450113:55450113(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1326C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000309964
Start 55453783:55453783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1024C>T
Mutation Classification Silent
Feature Type Transcript