Primary Site >> Liver Cancer

Gene >> IVL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368764
Start 152910291:152910291(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.494A>C
AA Mutation p.His165Pro(p.H165P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368764
Start 152910968:152910968(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1171G>A
AA Mutation p.Gly391Arg(p.G391R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368764
Start 152910723:152910723(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.926A>G
AA Mutation p.Gln309Arg(p.Q309R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368764
Start 152910623:152910623(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs541702541
CDS Mutation c.826C>T
AA Mutation p.Pro276Ser(p.P276S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368764
Start 152910686:152910686(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.889G>A
AA Mutation p.Asp297Asn(p.D297N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368764
Start 152909840:152909840(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.43C>A
AA Mutation p.Leu15Ile(p.L15I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000368764
Start 152911408:152911408(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1611G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000368764
Start 152911168:152911168(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1371G>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000368764
Start 152911280:152911280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1483C>T
AA Mutation p.Gln495Ter(p.Q495*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript