Primary Site >> Pancreatic Cancer

Gene >> MAPT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262410
Start 45983306:45983306(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770059067
CDS Mutation c.502C>T
AA Mutation p.Arg168Cys(p.R168C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262410
Start 45983307:45983307(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.503G>A
AA Mutation p.Arg168His(p.R168H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262410
Start 45974436:45974436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780582778
CDS Mutation c.272C>T
AA Mutation p.Ala91Val(p.A91V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262410
Start 45983446:45983446(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.642C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262410
Start 45983485:45983485(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.681C>A
Mutation Classification Silent
Feature Type Transcript