Primary Site >> Esophagus Cancer

Gene >> POSTN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379747
Start 37580649:37580649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1441A>G
AA Mutation p.Arg481Gly(p.R481G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379747
Start 37582463:37582463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1295A>C
AA Mutation p.His432Pro(p.H432P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379747
Start 37579351:37579351(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1669A>C
AA Mutation p.Asn557His(p.N557H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379747
Start 37580585:37580585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1505A>C
AA Mutation p.Lys502Thr(p.K502T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379747
Start 37584844:37584844(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.980A>G
AA Mutation p.Asn327Ser(p.N327S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379747
Start 37592107:37592107(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.276C>G
AA Mutation p.Cys92Trp(p.C92W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000379747
Start 37577775:37577775(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1986A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000379747
Start 37590402:37590402(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.411G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000379747
Start 37580649:37580649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1441A>T
AA Mutation p.Arg481Ter(p.R481*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript