Primary Site >> Liver Cancer

Gene >> SPEN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375759
Start 15931163:15931163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4923T>G
AA Mutation p.Ser1641Arg(p.S1641R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375759
Start 15930053:15930053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3813A>C
AA Mutation p.Glu1271Asp(p.E1271D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375759
Start 15932835:15932835(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550359408
CDS Mutation c.6595G>T
AA Mutation p.Ala2199Ser(p.A2199S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375759
Start 15935367:15935367(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9127A>G
AA Mutation p.Ser3043Gly(p.S3043G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000375759
Start 15928954:15928954(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768180417
CDS Mutation c.2714A>G
AA Mutation p.Asn905Ser(p.N905S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000375759
Start 15873021:15873021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.289A>G
AA Mutation p.Ile97Val(p.I97V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000375759
Start 15937198:15937198(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10062T>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000375759
Start 15934317:15934317(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8077C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000375759
Start 15929406:15929406(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3166A>T
AA Mutation p.Arg1056Ter(p.R1056*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript