Primary Site >> Pancreatic Cancer

Gene >> MKI67

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368654
Start 128103688:128103688(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8152G>A
AA Mutation p.Ala2718Thr(p.A2718T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368654
Start 128106081:128106081(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5759T>C
AA Mutation p.Phe1920Ser(p.F1920S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368654
Start 128107047:128107047(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs78597473
CDS Mutation c.4793G>A
AA Mutation p.Arg1598Gln(p.R1598Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368654
Start 128107264:128107264(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754283069
CDS Mutation c.4576G>A
AA Mutation p.Ala1526Thr(p.A1526T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368654
Start 128105120:128105120(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6720G>C
AA Mutation p.Lys2240Asn(p.K2240N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000368654
Start 128105309:128105309(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6531C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000368654
Start 128108090:128108090(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3750C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000368654
Start 128108762:128108762(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3078G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000368654
Start 128114947:128114947(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1461C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000368654
Start 128115769:128115769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.639C>T
Mutation Classification Silent
Feature Type Transcript