Primary Site >> Stomach Cancer

Gene >> QRSL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369046
Start 106640388:106640388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.64G>A
AA Mutation p.Glu22Lys(p.E22K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369046
Start 106649086:106649086(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.442T>A
AA Mutation p.Tyr148Asn(p.Y148N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369046
Start 106652345:106652345(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144191952
CDS Mutation c.694A>G
AA Mutation p.Ile232Val(p.I232V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369046
Start 106663135:106663135(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1316G>T
AA Mutation p.Arg439Ile(p.R439I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000369046
Start 106643061:106643061(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.355delA
AA Mutation p.Thr119GlnfsTer3(p.T119Qfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000369046
Start 106640471:106640471(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.150delA
AA Mutation p.Lys50AsnfsTer19(p.K50Nfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000369046
Start 106640398:106640398(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.78delA
AA Mutation p.Lys26AsnfsTer12(p.K26Nfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript