Primary Site >> Liver Cancer

Gene >> RIMS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72097008:72097008(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.305C>A
AA Mutation p.Ala102Glu(p.A102E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72307366:72307366(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140943787
CDS Mutation c.3959C>T
AA Mutation p.Ser1320Phe(p.S1320F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72259066:72259066(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3008A>T
AA Mutation p.His1003Leu(p.H1003L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72182561:72182561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1090T>G
AA Mutation p.Tyr364Asp(p.Y364D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72182327:72182327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.856C>G
AA Mutation p.Leu286Val(p.L286V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72258217:72258217(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2863T>C
AA Mutation p.Ser955Pro(p.S955P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72259026:72259026(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2968C>A
AA Mutation p.Pro990Thr(p.P990T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 71969017:71969017(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.199T>C
AA Mutation p.Cys67Arg(p.C67R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72392763:72392763(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4571G>A
AA Mutation p.Gly1524Glu(p.G1524E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000521978
Start 72333607:72333607(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4138A>G
AA Mutation p.Thr1380Ala(p.T1380A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000521978
Start 72392728:72392728(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4536T>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000521978
Start 72392782:72392782(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4590C>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000521978
Start 72307343:72307343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3936A>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000521978
Start 72291941:72291941(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3745C>A
Mutation Classification Silent
Feature Type Transcript