Primary Site >> Liver Cancer

Gene >> PARD3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374789
Start 34401830:34401830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.802C>G
AA Mutation p.Leu268Val(p.L268V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000374789
Start 34269658:34269658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3427A>G
AA Mutation p.Ser1143Gly(p.S1143G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374789
Start 34470230:34470230(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.437C>T
AA Mutation p.Pro146Leu(p.P146L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374789
Start 34382587:34382587(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780725925
CDS Mutation c.1352A>G
AA Mutation p.Tyr451Cys(p.Y451C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000374789
Start 34401845:34401845(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.787A>G
AA Mutation p.Ile263Val(p.I263V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000374789
Start 34382886:34382886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1053C>T
Mutation Classification Silent
Feature Type Transcript