Primary Site >> Stomach Cancer

Gene >> CCND2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261254
Start 4299894:4299894(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781695497
CDS Mutation c.755C>T
AA Mutation p.Ala252Val(p.A252V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261254
Start 4299886:4299886(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149961693
CDS Mutation c.747G>T
AA Mutation p.Gln249His(p.Q249H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261254
Start 4278872:4278872(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143681287
CDS Mutation c.524C>T
AA Mutation p.Ser175Phe(p.S175F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000261254
Start 4276037:4276037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.228C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261254
Start 4299940:4299940(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199959738
CDS Mutation c.801C>T
Mutation Classification Silent
Feature Type Transcript