Primary Site >> Esophagus Cancer

Gene >> SMARCD2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000448276
Start 63834196:63834196(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1054T>C
AA Mutation p.Tyr352His(p.Y352H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000448276
Start 63833679:63833679(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1225G>A
AA Mutation p.Asp409Asn(p.D409N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000448276
Start 63834542:63834542(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.853G>A
AA Mutation p.Gly285Ser(p.G285S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000448276
Start 63833710:63833710(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201339780
CDS Mutation c.1194C>T
Mutation Classification Silent
Feature Type Transcript