Primary Site >> Stomach Cancer

Gene >> GSK3B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264235
Start 119912775:119912775(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.644C>T
AA Mutation p.Ser215Leu(p.S215L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264235
Start 120002053:120002053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.275G>T
AA Mutation p.Arg92Ile(p.R92I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264235
Start 119916101:119916101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.551C>T
AA Mutation p.Pro184Leu(p.P184L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264235
Start 119947345:119947345(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.289G>A
AA Mutation p.Glu97Lys(p.E97K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264235
Start 119843261:119843261(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1189G>A
AA Mutation p.Ala397Thr(p.A397T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264235
Start 120002125:120002125(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.203G>T
AA Mutation p.Gly68Val(p.G68V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264235
Start 119916103:119916103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.549A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000264235
Start 119912811:119912811(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.609-1G>C
Mutation Classification Splice_Site
Feature Type Transcript