Primary Site >> Liver Cancer

Gene >> SLIT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266058
Start 97006651:97006651(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3411G>T
AA Mutation p.Gln1137His(p.Q1137H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266058
Start 97002890:97002890(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3968T>A
AA Mutation p.Leu1323Gln(p.L1323Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266058
Start 97164826:97164826(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770689075
CDS Mutation c.262C>T
AA Mutation p.Arg88Trp(p.R88W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266058
Start 97002205:97002205(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4319C>T
AA Mutation p.Ala1440Val(p.A1440V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266058
Start 97002723:97002723(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373006664
CDS Mutation c.4135G>A
AA Mutation p.Gly1379Ser(p.G1379S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000266058
Start 97004809:97004809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3594G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000266058
Start 97185651:97185651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.24G>A
Mutation Classification Silent
Feature Type Transcript