Primary Site >> Liver Cancer

Gene >> MAP1A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43528555:43528555(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7082G>A
AA Mutation p.Gly2361Asp(p.G2361D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522978:43522978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1505C>T
AA Mutation p.Pro502Leu(p.P502L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43523145:43523145(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1672C>A
AA Mutation p.Pro558Thr(p.P558T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43527201:43527201(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764432579
CDS Mutation c.5728C>T
AA Mutation p.Arg1910Cys(p.R1910C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43529248:43529248(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7775T>A
AA Mutation p.Val2592Glu(p.V2592E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43524267:43524267(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2794T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43526975:43526975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5502T>A
Mutation Classification Silent
Feature Type Transcript