Primary Site >> Liver Cancer

Gene >> ROBO1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78688718:78688718(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1100C>A
AA Mutation p.Thr367Asn(p.T367N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 79125501:79125501(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.127C>T
AA Mutation p.Pro43Ser(p.P43S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78651864:78651864(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2680G>A
AA Mutation p.Val894Met(p.V894M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78657166:78657166(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2546G>A
AA Mutation p.Ser849Asn(p.S849N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78635831:78635831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3315G>T
AA Mutation p.Gln1105His(p.Q1105H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78662063:78662063(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2018T>A
AA Mutation p.Leu673Gln(p.L673Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78639826:78639826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2955C>A
AA Mutation p.Asn985Lys(p.N985K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78617681:78617681(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4236G>T
AA Mutation p.Glu1412Asp(p.E1412D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000464233
Start 78714472:78714472(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.970G>T
AA Mutation p.Asp324Tyr(p.D324Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000464233
Start 78635864:78635864(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3282T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000464233
Start 78657117:78657117(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2595G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000464233
Start 78668223:78668223(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1710A>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000464233
Start 78651925:78651925(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2619C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000464233
Start 78600216:78600216(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4838delG
AA Mutation p.Gly1613GlufsTer10(p.G1613Efs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000464233
Start 79589885:79589886(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.26dupT
AA Mutation p.Leu9PhefsTer24(p.L9Ffs*24)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript