Primary Site >> Stomach Cancer

Gene >> RAB11FIP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355624
Start 118046067:118046067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.97A>G
AA Mutation p.Thr33Ala(p.T33A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355624
Start 118045976:118045976(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.188A>G
AA Mutation p.Glu63Gly(p.E63G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355624
Start 118038987:118038987(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774506108
CDS Mutation c.1250T>C
AA Mutation p.Ile417Thr(p.I417T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000355624
Start 118046160:118046160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4A>C
AA Mutation p.Met2Leu(p.M2L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000355624
Start 118039304:118039304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.933A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000355624
Start 118045815:118045815(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.349delA
AA Mutation p.Thr117GlnfsTer6(p.T117Qfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000355624
Start 118039136:118039136(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1101delA
AA Mutation p.Asp368IlefsTer19(p.D368Ifs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000355624
Start 118040280:118040281(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.638dupA
AA Mutation p.Pro214AlafsTer17(p.P214Afs*17)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000355624
Start 118039135:118039136(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1101dupA
AA Mutation p.Asp368ArgfsTer2(p.D368Rfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript