Primary Site >> Stomach Cancer

Gene >> GAS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000298743
Start 86945914:86945914(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.866G>A
AA Mutation p.Gly289Asp(p.G289D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000298743
Start 86946157:86946157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.623A>G
AA Mutation p.Glu208Gly(p.E208G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000298743
Start 86945992:86945992(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.788A>G
AA Mutation p.Asp263Gly(p.D263G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000298743
Start 86946247:86946247(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.533G>A
AA Mutation p.Arg178His(p.R178H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000298743
Start 86945984:86945984(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.796G>A
AA Mutation p.Asp266Asn(p.D266N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000298743
Start 86945932:86945932(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.848C>T
AA Mutation p.Pro283Leu(p.P283L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000298743
Start 86945949:86945949(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.831C>T
Mutation Classification Silent
Feature Type Transcript