Primary Site >> Stomach Cancer

Gene >> TCEA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000521604
Start 53988216:53988216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.364G>A
AA Mutation p.Ala122Thr(p.A122T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000521604
Start 53979138:53979138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.712A>G
AA Mutation p.Lys238Glu(p.K238E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000521604
Start 53988158:53988158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.422G>A
AA Mutation p.Arg141Gln(p.R141Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000521604
Start 53979126:53979126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.724A>G
AA Mutation p.Lys242Glu(p.K242E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000521604
Start 53993697:53993697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.291G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000521604
Start 53979106:53979106(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.744T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000521604
Start 53986968:53986968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.523+1A>G
Mutation Classification Splice_Site
Feature Type Transcript