Primary Site >> Pancreatic Cancer

Gene >> ASPM

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197103156:197103156(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149033840
CDS Mutation c.6095G>A
AA Mutation p.Arg2032His(p.R2032H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197100499:197100499(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8752G>T
AA Mutation p.Ala2918Ser(p.A2918S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197103301:197103301(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5950C>A
AA Mutation p.His1984Asn(p.H1984N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197103403:197103403(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5848G>T
AA Mutation p.Ala1950Ser(p.A1950S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197122007:197122007(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3778C>A
AA Mutation p.Leu1260Ile(p.L1260I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197128535:197128535(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2891C>T
AA Mutation p.Ala964Val(p.A964V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197142703:197142703(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1549G>A
AA Mutation p.Ala517Thr(p.A517T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000367409
Start 197101255:197101255(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7996A>G
AA Mutation p.Thr2666Ala(p.T2666A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000367409
Start 197103029:197103029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6222G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000367409
Start 197143693:197143693(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.559A>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000367409
Start 197101987:197101987(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7264C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000367409
Start 197103793:197103793(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5458C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000367409
Start 197102252:197102252(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6999G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000367409
Start 197104883:197104883(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4368G>A
AA Mutation p.Trp1456Ter(p.W1456*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript