Primary Site >> Stomach Cancer

Gene >> NF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338641
Start 29642236:29642236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.398G>A
AA Mutation p.Cys133Tyr(p.C133Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338641
Start 29678223:29678223(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1474C>T
AA Mutation p.Pro492Ser(p.P492S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338641
Start 29671893:29671893(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1067T>G
AA Mutation p.Leu356Trp(p.L356W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338641
Start 29668384:29668384(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.937G>T
AA Mutation p.Ala313Ser(p.A313S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000338641
Start 29681463:29681463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1599G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000338641
Start 29661243:29661243(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.714C>A
Mutation Classification Silent
Feature Type Transcript