Primary Site >> Stomach Cancer

Gene >> TMEM119

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000392806
Start 108591692:108591692(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151298360
CDS Mutation c.692C>T
AA Mutation p.Ala231Val(p.A231V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000392806
Start 108592050:108592050(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773723919
CDS Mutation c.334G>A
AA Mutation p.Val112Ile(p.V112I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000392806
Start 108591875:108591875(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201913296
CDS Mutation c.509G>A
AA Mutation p.Arg170Gln(p.R170Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000392806
Start 108591947:108591947(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752298653
CDS Mutation c.437G>C
AA Mutation p.Gly146Ala(p.G146A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000392806
Start 108592243:108592243(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs528443188
CDS Mutation c.141G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000392806
Start 108591961:108591961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.423T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000392806
Start 108592157:108592157(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.227delG
AA Mutation p.Gly76AlafsTer12(p.G76Afs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript