Primary Site >> Liver Cancer

Gene >> EPHA7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369303
Start 93259368:93259368(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1910G>C
AA Mutation p.Arg637Pro(p.R637P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369303
Start 93410860:93410860(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.473G>A
AA Mutation p.Gly158Asp(p.G158D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369303
Start 93410653:93410653(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.680T>C
AA Mutation p.Leu227Ser(p.L227S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000369303
Start 93259385:93259385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1893C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000369303
Start 93414751:93414751(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.114T>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000369303
Start 93258147:93258147(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2062C>T
AA Mutation p.Gln688Ter(p.Q688*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000369303
Start 93245299:93245299(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2881G>T
AA Mutation p.Glu961Ter(p.E961*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript