Primary Site >> Esophagus Cancer

Gene >> PIWIL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000245255
Start 130349307:130349307(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.803A>G
AA Mutation p.Asp268Gly(p.D268G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000245255
Start 130361222:130361222(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1708G>A
AA Mutation p.Ala570Thr(p.A570T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000245255
Start 130349359:130349359(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.855C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000245255
Start 130349266:130349266(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.762T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000245255
Start 130362820:130362820(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2025C>G
Mutation Classification Silent
Feature Type Transcript