Primary Site >> Pancreatic Cancer

Gene >> TRPS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000220888
Start 115604098:115604098(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762850704
CDS Mutation c.1832G>A
AA Mutation p.Arg611Gln(p.R611Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000220888
Start 115414892:115414892(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2977C>G
AA Mutation p.Gln993Glu(p.Q993E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000220888
Start 115604356:115604356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1574G>A
AA Mutation p.Cys525Tyr(p.C525Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000220888
Start 115604885:115604885(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757182048
CDS Mutation c.1045G>A
AA Mutation p.Glu349Lys(p.E349K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000220888
Start 115418432:115418432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2682T>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000220888
Start 115587414:115587414(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2248C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000220888
Start 115414041:115414042(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3827dupA
AA Mutation p.Asn1276LysfsTer5(p.N1276Kfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript