Primary Site >> Liver Cancer

Gene >> JARID2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000341776
Start 15501023:15501023(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2062A>G
AA Mutation p.Arg688Gly(p.R688G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000341776
Start 15468622:15468622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.574A>T
AA Mutation p.Thr192Ser(p.T192S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000341776
Start 15496606:15496606(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1381A>G
AA Mutation p.Lys461Glu(p.K461E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000341776
Start 15468634:15468634(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.586A>C
AA Mutation p.Lys196Gln(p.K196Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000341776
Start 15507393:15507393(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2708T>A
AA Mutation p.Leu903Gln(p.L903Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000341776
Start 15452125:15452125(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.443C>G
AA Mutation p.Ser148Cys(p.S148C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000341776
Start 15497067:15497067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1842C>T
Mutation Classification Silent
Feature Type Transcript