Primary Site >> Pancreatic Cancer

Gene >> DYNC2H1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375735
Start 103304685:103304685(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11347C>A
AA Mutation p.His3783Asn(p.H3783N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375735
Start 103192223:103192223(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7667T>G
AA Mutation p.Phe2556Cys(p.F2556C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375735
Start 103215770:103215770(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8744A>T
AA Mutation p.Asn2915Ile(p.N2915I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375735
Start 103222974:103222974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9241C>T
AA Mutation p.Arg3081Cys(p.R3081C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000375735
Start 103287564:103287564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11054G>T
AA Mutation p.Arg3685Ile(p.R3685I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000375735
Start 103321121:103321121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11818C>T
AA Mutation p.Leu3940Phe(p.L3940F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000375735
Start 103135726:103135726(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2352A>G
Mutation Classification Silent
Feature Type Transcript