Primary Site >> Stomach Cancer

Gene >> ENOX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43322495:43322495(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748351168
CDS Mutation c.1150C>T
AA Mutation p.Arg384Trp(p.R384W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43214078:43214078(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761977987
CDS Mutation c.1844G>A
AA Mutation p.Arg615His(p.R615H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43412892:43412892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.23A>G
AA Mutation p.Glu8Gly(p.E8G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43359865:43359865(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.575C>T
AA Mutation p.Ala192Val(p.A192V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43361395:43361395(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.266C>A
AA Mutation p.Pro89His(p.P89H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43322483:43322483(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1162A>T
AA Mutation p.Ser388Cys(p.S388C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43359988:43359988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.452A>G
AA Mutation p.Glu151Gly(p.E151G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43344561:43344561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013C>T
AA Mutation p.Ala338Val(p.A338V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43224065:43224065(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1788G>T
AA Mutation p.Gln596His(p.Q596H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261488
Start 43412030:43412030(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.94G>C
AA Mutation p.Ala32Pro(p.A32P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000261488
Start 43360002:43360002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747550444
CDS Mutation c.438C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000261488
Start 43355956:43355956(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.786G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000261488
Start 43344719:43344719(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.855G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000261488
Start 43322463:43322463(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1182C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000261488
Start 43322450:43322450(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1195G>T
AA Mutation p.Glu399Ter(p.E399*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000261488
Start 43326520:43326520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1042C>T
AA Mutation p.Gln348Ter(p.Q348*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000261488
Start 43298387:43298387(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1405C>T
AA Mutation p.Gln469Ter(p.Q469*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript