Primary Site >> Stomach Cancer

Gene >> CCNE1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262643
Start 29822501:29822501(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1008G>T
AA Mutation p.Met336Ile(p.M336I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262643
Start 29817503:29817503(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.424C>T
AA Mutation p.Pro142Ser(p.P142S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262643
Start 29822550:29822550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1057G>A
AA Mutation p.Ala353Thr(p.A353T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262643
Start 29820771:29820771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.532G>A
AA Mutation p.Ala178Thr(p.A178T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262643
Start 29817513:29817513(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434G>A
AA Mutation p.Arg145Gln(p.R145Q)
Mutation Classification Missense_Mutation
Feature Type Transcript