Primary Site >> Liver Cancer

Gene >> PTPN22

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113829981:113829981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2102C>G
AA Mutation p.Thr701Ser(p.T701S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113856607:113856607(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs115552198
CDS Mutation c.421C>T
AA Mutation p.Arg141Cys(p.R141C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113838226:113838226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1174G>A
AA Mutation p.Asp392Asn(p.D392N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359785
Start 113852028:113852028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.827A>C
AA Mutation p.Gln276Pro(p.Q276P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113838073:113838073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1327C>A
AA Mutation p.Pro443Thr(p.P443T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113838192:113838192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1208C>T
AA Mutation p.Pro403Leu(p.P403L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000359785
Start 113837669:113837669(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1731T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000359785
Start 113838212:113838212(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1188A>G
Mutation Classification Silent
Feature Type Transcript