Primary Site >> Pancreatic Cancer

Gene >> NLGN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000457714
Start 174280819:174280819(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1988G>A
AA Mutation p.Ser663Asn(p.S663N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000457714
Start 174278873:174278873(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.872G>A
AA Mutation p.Arg291Gln(p.R291Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000457714
Start 174279209:174279209(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1208A>G
AA Mutation p.Asp403Gly(p.D403G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000457714
Start 174279370:174279370(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1369C>A
AA Mutation p.Leu457Met(p.L457M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000457714
Start 174281095:174281095(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs527860138
CDS Mutation c.2264G>A
AA Mutation p.Arg755Gln(p.R755Q)
Mutation Classification Missense_Mutation
Feature Type Transcript