Primary Site >> Stomach Cancer

Gene >> VGLL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370634
Start 136548888:136548888(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.514C>A
AA Mutation p.Leu172Ile(p.L172I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370634
Start 136548694:136548694(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.320C>T
AA Mutation p.Pro107Leu(p.P107L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370634
Start 136548828:136548828(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769583709
CDS Mutation c.454G>A
AA Mutation p.Ala152Thr(p.A152T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370634
Start 136548930:136548930(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768578233
CDS Mutation c.556G>A
AA Mutation p.Ala186Thr(p.A186T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370634
Start 136548978:136548978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.604C>T
AA Mutation p.Leu202Phe(p.L202F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370634
Start 136548696:136548696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.322G>A
AA Mutation p.Gly108Ser(p.G108S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000370634
Start 136556487:136556487(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.725T>G
AA Mutation p.Leu242Arg(p.L242R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000370634
Start 136548953:136548953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.579C>T
Mutation Classification Silent
Feature Type Transcript