Primary Site >> Esophagus Cancer

Gene >> NT5C1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359846
Start 18584192:18584192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.967G>A
AA Mutation p.Gly323Ser(p.G323S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000359846
Start 18582881:18582881(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780305599
CDS Mutation c.1188C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000359846
Start 18584868:18584868(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.549C>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant;start_lost
Transcription ID ENST00000359846
Start 18589468:18589468(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1delA
AA Mutation p.Met1?(p.M1?)
Mutation Classification Frame_Shift_Del
Feature Type Transcript