Primary Site >> Pancreatic Cancer

Gene >> MMRN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264790
Start 89936054:89936054(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2374G>A
AA Mutation p.Asp792Asn(p.D792N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264790
Start 89935371:89935371(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1691T>C
AA Mutation p.Phe564Ser(p.F564S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264790
Start 89953035:89953035(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3304G>A
AA Mutation p.Ala1102Thr(p.A1102T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000264790
Start 89951690:89951690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3204A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000264790
Start 89951651:89951651(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778903851
CDS Mutation c.3165G>A
Mutation Classification Silent
Feature Type Transcript