Primary Site >> Stomach Cancer

Gene >> GABARAPL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266458
Start 10221811:10221811(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.313C>A
AA Mutation p.Leu105Met(p.L105M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266458
Start 10220554:10220554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.284A>G
AA Mutation p.Tyr95Cys(p.Y95C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266458
Start 10218091:10218091(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.119G>T
AA Mutation p.Arg40Met(p.R40M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266458
Start 10213172:10213172(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.43A>G
AA Mutation p.Lys15Glu(p.K15E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266458
Start 10218096:10218096(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749513430
CDS Mutation c.124C>T
AA Mutation p.Pro42Ser(p.P42S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000266458
Start 10220516:10220516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.246C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000266458
Start 10221786:10221786(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.289-1G>A
Mutation Classification Splice_Site
Feature Type Transcript