Primary Site >> Pancreatic Cancer

Gene >> MAP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209693845:209693845(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1675G>C
AA Mutation p.Asp559His(p.D559H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209695100:209695100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2930C>T
AA Mutation p.Ala977Val(p.A977V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694284:209694284(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146432517
CDS Mutation c.2114C>T
AA Mutation p.Pro705Leu(p.P705L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209696094:209696094(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368301391
CDS Mutation c.3924C>T
Mutation Classification Silent
Feature Type Transcript