Primary Site >> Stomach Cancer

Gene >> ADRA1D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248647:4248647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.311C>T
AA Mutation p.Ala104Val(p.A104V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248450:4248450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.508G>A
AA Mutation p.Asp170Asn(p.D170N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248429:4248429(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745387589
CDS Mutation c.529G>A
AA Mutation p.Val177Met(p.V177M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248243:4248243(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.715G>A
AA Mutation p.Val239Met(p.V239M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4221791:4221791(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1451T>A
AA Mutation p.Val484Asp(p.V484D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4221531:4221531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1711G>A
AA Mutation p.Asp571Asn(p.D571N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000379453
Start 4247851:4247851(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1107G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000379453
Start 4221610:4221610(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1632A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000379453
Start 4221574:4221574(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1668C>T
Mutation Classification Silent
Feature Type Transcript