Primary Site >> Esophagus Cancer

Gene >> PZP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261336
Start 9202366:9202366(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.433T>C
AA Mutation p.Phe145Leu(p.F145L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261336
Start 9150728:9150728(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4300A>G
AA Mutation p.Ser1434Gly(p.S1434G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261336
Start 9150728:9150728(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4300A>C
AA Mutation p.Ser1434Arg(p.S1434R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261336
Start 9160397:9160397(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2966A>G
AA Mutation p.Asn989Ser(p.N989S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261336
Start 9152874:9152874(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4071T>G
Mutation Classification Silent
Feature Type Transcript