Primary Site >> Stomach Cancer

Gene >> CCND1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000227507
Start 69643073:69643073(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.241G>A
AA Mutation p.Ala81Thr(p.A81T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000227507
Start 69651205:69651205(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759765773
CDS Mutation c.811G>A
AA Mutation p.Ala271Thr(p.A271T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000227507
Start 69643991:69643991(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.574G>T
AA Mutation p.Asp192Tyr(p.D192Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000227507
Start 69648049:69648049(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146267501
CDS Mutation c.630C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000227507
Start 69641451:69641451(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.138A>G
Mutation Classification Silent
Feature Type Transcript