Primary Site >> Esophagus Cancer

Gene >> ITPR3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374316
Start 33684143:33684143(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4912T>C
AA Mutation p.Cys1638Arg(p.C1638R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374316
Start 33685804:33685804(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5644G>C
AA Mutation p.Glu1882Gln(p.E1882Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000374316
Start 33693672:33693672(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs183531106
CDS Mutation c.7752G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000374316
Start 33678456:33678456(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543118868
CDS Mutation c.3684G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000374316
Start 33685409:33685409(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747022423
CDS Mutation c.5358C>T
Mutation Classification Silent
Feature Type Transcript