Primary Site >> Stomach Cancer

Gene >> UQCRC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000203407
Start 48599683:48599683(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1330A>C
AA Mutation p.Ile444Leu(p.I444L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000203407
Start 48609163:48609163(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.209C>A
AA Mutation p.Thr70Lys(p.T70K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000203407
Start 48601354:48601354(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.820G>A
AA Mutation p.Glu274Lys(p.E274K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000203407
Start 48601044:48601044(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141289289
CDS Mutation c.897G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000203407
Start 48600089:48600089(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1276delC
AA Mutation p.Leu426TrpfsTer89(p.L426Wfs*89)
Mutation Classification Frame_Shift_Del
Feature Type Transcript