Primary Site >> Pancreatic Cancer

Gene >> MED1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300651
Start 39408496:39408496(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3725G>A
AA Mutation p.Gly1242Asp(p.G1242D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000300651
Start 39409332:39409332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2889A>C
AA Mutation p.Leu963Phe(p.L963F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000300651
Start 39408319:39408319(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756858854
CDS Mutation c.3902C>T
AA Mutation p.Pro1301Leu(p.P1301L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000300651
Start 39415088:39415088(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1437C>T
Mutation Classification Silent
Feature Type Transcript