Primary Site >> Liver Cancer

Gene >> MAP1S

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324096
Start 17720977:17720977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.160G>C
AA Mutation p.Asp54His(p.D54H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324096
Start 17725061:17725061(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.316C>G
AA Mutation p.Leu106Val(p.L106V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324096
Start 17719576:17719576(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.74G>A
AA Mutation p.Gly25Glu(p.G25E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000324096
Start 17726869:17726869(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1485C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000324096
Start 17726596:17726596(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374141963
CDS Mutation c.1212C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000324096
Start 17726425:17726425(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1041G>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000324096
Start 17726747:17726747(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1363C>T
AA Mutation p.Arg455Ter(p.R455*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript