Primary Site >> Pancreatic Cancer

Gene >> SLIT2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000504154
Start 20524169:20524169(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192894188
CDS Mutation c.1430G>A
AA Mutation p.Arg477His(p.R477H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000504154
Start 20542559:20542559(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2209G>T
AA Mutation p.Val737Phe(p.V737F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000504154
Start 20567265:20567265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2729C>A
AA Mutation p.Pro910His(p.P910H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000504154
Start 20548515:20548515(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2373G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000504154
Start 20598333:20598333(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3630C>A
Mutation Classification Silent
Feature Type Transcript