Primary Site >> Pancreatic Cancer

Gene >> FMN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240093286:240093286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1177G>A
AA Mutation p.Ala393Thr(p.A393T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000319653
Start 240207802:240207802(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2990T>C
AA Mutation p.Ile997Thr(p.I997T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240206825:240206825(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs568308648
CDS Mutation c.2013A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240207068:240207068(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140392779
CDS Mutation c.2256C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000319653
Start 240211220:240211220(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4050G>A
Mutation Classification Silent
Feature Type Transcript