Primary Site >> Liver Cancer

Gene >> PRDM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000235372
Start 13749420:13749420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.444A>G
AA Mutation p.Ile148Met(p.I148M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000235372
Start 13779311:13779311(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1516C>T
AA Mutation p.His506Tyr(p.H506Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000235372
Start 13749392:13749392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.416G>T
AA Mutation p.Trp139Leu(p.W139L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000235372
Start 13781743:13781743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3948A>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000235372
Start 13749471:13749471(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.495C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000235372
Start 13782133:13782133(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4338G>A
Mutation Classification Silent
Feature Type Transcript