Primary Site >> Liver Cancer

Gene >> FCRL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368176
Start 157801951:157801951(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200955967
CDS Mutation c.850G>A
AA Mutation p.Ala284Thr(p.A284T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000368176
Start 157802664:157802664(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.320G>T
AA Mutation p.Arg107Met(p.R107M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368176
Start 157796164:157796164(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1225T>A
AA Mutation p.Leu409Ile(p.L409I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000368176
Start 157801575:157801575(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.889C>T
AA Mutation p.Pro297Ser(p.P297S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368176
Start 157796103:157796103(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1286T>C
AA Mutation p.Met429Thr(p.M429T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368176
Start 157802532:157802532(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.452C>A
AA Mutation p.Ala151Asp(p.A151D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000368176
Start 157798221:157798221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1054C>A
AA Mutation p.Gln352Lys(p.Q352K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000368176
Start 157802501:157802501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.483G>A
Mutation Classification Silent
Feature Type Transcript