Primary Site >> Stomach Cancer

Gene >> IGSF11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118902591:118902591(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769083075
CDS Mutation c.1225G>A
AA Mutation p.Ala409Thr(p.A409T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118902767:118902767(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1049G>A
AA Mutation p.Gly350Asp(p.G350D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118902578:118902578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1238G>A
AA Mutation p.Arg413Gln(p.R413Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118905713:118905713(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140836568
CDS Mutation c.586G>A
AA Mutation p.Val196Ile(p.V196I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118902525:118902525(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1291G>A
AA Mutation p.Val431Ile(p.V431I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118902606:118902606(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1210T>C
AA Mutation p.Tyr404His(p.Y404H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118904686:118904686(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.816T>G
AA Mutation p.Asn272Lys(p.N272K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118902539:118902539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1277G>A
AA Mutation p.Arg426Gln(p.R426Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000393775
Start 118902950:118902950(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.866T>C
AA Mutation p.Leu289Pro(p.L289P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000393775
Start 118930181:118930181(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746094445
CDS Mutation c.147C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000393775
Start 118926156:118926156(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.525T>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000393775
Start 118902619:118902619(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146853299
CDS Mutation c.1197A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000393775
Start 118926177:118926177(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.504G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000393775
Start 118926156:118926156(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377330100
CDS Mutation c.525T>C
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000393775
Start 118926129:118926129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.552C>A
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000393775
Start 118902819:118902819(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.997G>T
AA Mutation p.Glu333Ter(p.E333*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000393775
Start 118904760:118904761(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.741dupT
AA Mutation p.Gly248TrpfsTer26(p.G248Wfs*26)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript