Primary Site >> Esophagus Cancer

Gene >> PRDM16

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000270722
Start 3432099:3432099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3655G>C
AA Mutation p.Glu1219Gln(p.E1219Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000270722
Start 3412124:3412124(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1927G>T
AA Mutation p.Ala643Ser(p.A643S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000270722
Start 3412517:3412517(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2320G>T
AA Mutation p.Asp774Tyr(p.D774Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000270722
Start 3412588:3412588(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370931714
CDS Mutation c.2391C>T
Mutation Classification Silent
Feature Type Transcript