Primary Site >> Pancreatic Cancer

Gene >> DHX36

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000496811
Start 154300663:154300663(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1392G>A
AA Mutation p.Met464Ile(p.M464I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000496811
Start 154277630:154277630(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2656C>T
AA Mutation p.Leu886Phe(p.L886F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000496811
Start 154284935:154284935(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752340783
CDS Mutation c.2084G>A
AA Mutation p.Arg695Gln(p.R695Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000496811
Start 154315099:154315099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.550T>G
AA Mutation p.Leu184Val(p.L184V)
Mutation Classification Missense_Mutation
Feature Type Transcript