Primary Site >> Pancreatic Cancer

Gene >> DNMT3A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25244195:25244195(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759818409
CDS Mutation c.1811G>A
AA Mutation p.Arg604Gln(p.R604Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25239169:25239169(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2369G>T
AA Mutation p.Arg790Met(p.R790M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25244161:25244161(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1845G>T
AA Mutation p.Gln615His(p.Q615H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25246706:25246706(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1193C>T
AA Mutation p.Ala398Val(p.A398V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25245257:25245257(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1550G>C
AA Mutation p.Cys517Ser(p.C517S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000264709
Start 25237004:25237004(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2410C>T
AA Mutation p.Pro804Ser(p.P804S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264709
Start 25282691:25282691(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.198A>G
Mutation Classification Silent
Feature Type Transcript