Primary Site >> Liver Cancer

Gene >> PTPN13

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86701670:86701670(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1064G>A
AA Mutation p.Gly355Asp(p.G355D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86635318:86635318(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.62T>C
AA Mutation p.Ile21Thr(p.I21T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86771427:86771427(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5060T>A
AA Mutation p.Val1687Glu(p.V1687E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86771300:86771300(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4933T>C
AA Mutation p.Ser1645Pro(p.S1645P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86722316:86722316(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1490G>T
AA Mutation p.Arg497Ile(p.R497I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86780448:86780448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5938G>A
AA Mutation p.Ala1980Thr(p.A1980T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86635279:86635279(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.23C>A
AA Mutation p.Ala8Asp(p.A8D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86762733:86762733(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3560C>A
AA Mutation p.Ser1187Tyr(p.S1187Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86701783:86701783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1177G>A
AA Mutation p.Glu393Lys(p.E393K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86811100:86811100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7354C>A
AA Mutation p.Gln2452Lys(p.Q2452K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86734344:86734344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1900A>G
AA Mutation p.Lys634Glu(p.K634E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86701757:86701757(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1151G>T
AA Mutation p.Arg384Ile(p.R384I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86717067:86717067(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1335T>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence splice_donor_variant
Transcription ID ENST00000411767
Start 86689191:86689191(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.546+1G>T
Mutation Classification Splice_Site
Feature Type Transcript