Primary Site >> Liver Cancer

Gene >> ROBO2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77607840:77607840(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3179A>C
AA Mutation p.Lys1060Thr(p.K1060T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000461745
Start 77617515:77617515(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372099694
CDS Mutation c.3296A>G
AA Mutation p.Tyr1099Cys(p.Y1099C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77563202:77563202(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1555A>G
AA Mutation p.Ser519Gly(p.S519G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77546341:77546341(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761239340
CDS Mutation c.938C>T
AA Mutation p.Pro313Leu(p.P313L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77558104:77558104(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1392A>T
AA Mutation p.Arg464Ser(p.R464S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77622271:77622271(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3599C>A
AA Mutation p.Pro1200Gln(p.P1200Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77602395:77602395(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751528165
CDS Mutation c.3040G>A
AA Mutation p.Asp1014Asn(p.D1014N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77564995:77564995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1724T>C
AA Mutation p.Val575Ala(p.V575A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77580044:77580044(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2426A>C
AA Mutation p.Gln809Pro(p.Q809P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77574575:77574575(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2048C>T
AA Mutation p.Ser683Leu(p.S683L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77579982:77579982(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2364C>G
AA Mutation p.Ile788Met(p.I788M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77580063:77580063(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2445A>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77098048:77098048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.96G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence splice_donor_variant
Transcription ID ENST00000461745
Start 77098342:77098342(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.388+2T>C
Mutation Classification Splice_Site
Feature Type Transcript