Primary Site >> Stomach Cancer

Gene >> POU3F3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856459:104856459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.949C>T
AA Mutation p.Pro317Ser(p.P317S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856907:104856907(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1397C>T
AA Mutation p.Pro466Leu(p.P466L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856460:104856460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950C>T
AA Mutation p.Pro317Leu(p.P317L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856451:104856451(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.941A>T
AA Mutation p.Glu314Val(p.E314V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856897:104856897(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1387C>T
AA Mutation p.Arg463Cys(p.R463C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856741:104856741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1231A>G
AA Mutation p.Thr411Ala(p.T411A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856973:104856973(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1463C>T
AA Mutation p.Thr488Met(p.T488M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856831:104856831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1321G>A
AA Mutation p.Asp441Asn(p.D441N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856463:104856463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.953C>T
AA Mutation p.Thr318Met(p.T318M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856769:104856769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1259C>T
AA Mutation p.Ala420Val(p.A420V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856904:104856904(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1394C>T
AA Mutation p.Thr465Met(p.T465M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856532:104856532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1022C>T
AA Mutation p.Ala341Val(p.A341V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000361360
Start 104856508:104856508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.998G>A
AA Mutation p.Arg333His(p.R333H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000361360
Start 104856449:104856449(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.939C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000361360
Start 104857004:104857004(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1494C>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000361360
Start 104855714:104855714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.204C>A
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000361360
Start 104856464:104856464(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.954G>A
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000361360
Start 104856533:104856533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1023C>T
Mutation Classification Silent
Feature Type Transcript
ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000361360
Start 104856929:104856929(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1419G>A
Mutation Classification Silent
Feature Type Transcript