Primary Site >> Liver Cancer

Gene >> PTPRN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000389418
Start 158167110:158167110(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139278439
CDS Mutation c.731C>T
AA Mutation p.Ala244Val(p.A244V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000389418
Start 157576681:157576681(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2715G>T
AA Mutation p.Gln905His(p.Q905H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000389418
Start 158133761:158133761(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1472C>A
AA Mutation p.Ala491Asp(p.A491D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000389418
Start 157576741:157576741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2655C>G
AA Mutation p.Phe885Leu(p.F885L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000389418
Start 158316891:158316891(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.205T>A
AA Mutation p.Phe69Ile(p.F69I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000389418
Start 158138342:158138342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1084G>A
AA Mutation p.Glu362Lys(p.E362K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000389418
Start 158166989:158166989(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.852C>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000389418
Start 157576754:157576755(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2641_2642insAAGTGGCCGTGAACAGAATGTTGATAGAAATTTG
AA Mutation p.Trp881Ter(p.W881*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript