Primary Site >> Liver Cancer

Gene >> TPR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367478
Start 186326135:186326135(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5990G>A
AA Mutation p.Gly1997Asp(p.G1997D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367478
Start 186326220:186326220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5905G>A
AA Mutation p.Glu1969Lys(p.E1969K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000367478
Start 186322318:186322318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6461A>T
AA Mutation p.His2154Leu(p.H2154L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367478
Start 186355534:186355534(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2047A>C
AA Mutation p.Lys683Gln(p.K683Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000367478
Start 186358573:186358573(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1467G>C
AA Mutation p.Met489Ile(p.M489I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000367478
Start 186353841:186353841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2181G>T
AA Mutation p.Met727Ile(p.M727I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000367478
Start 186360318:186360318(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1146A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000367478
Start 186335497:186335497(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4752G>A
Mutation Classification Silent
Feature Type Transcript