Primary Site >> Pancreatic Cancer

Gene >> CHD3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000330494
Start 7903890:7903890(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3793G>A
AA Mutation p.Asp1265Asn(p.D1265N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000330494
Start 7897210:7897210(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1835C>A
AA Mutation p.Pro612Gln(p.P612Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000330494
Start 7900011:7900011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2660G>A
AA Mutation p.Arg887Gln(p.R887Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000330494
Start 7891032:7891032(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.477C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000330494
Start 7903298:7903298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3522C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000330494
Start 7907376:7907376(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4812A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000330494
Start 7910915:7910915(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5823G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000330494
Start 7907959:7907959(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5092C>T
AA Mutation p.Arg1698Ter(p.R1698*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000330494
Start 7890736:7890737(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.383dupA
AA Mutation p.Gln129AlafsTer25(p.Q129Afs*25)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript