Primary Site >> Stomach Cancer

Gene >> DOCK5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25300583:25300583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.772T>C
AA Mutation p.Tyr258His(p.Y258H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25323860:25323860(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781464699
CDS Mutation c.1628C>T
AA Mutation p.Ser543Leu(p.S543L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25296613:25296613(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571T>C
AA Mutation p.Ser191Pro(p.S191P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25366951:25366951(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs190638874
CDS Mutation c.3205C>T
AA Mutation p.Arg1069Cys(p.R1069C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25368661:25368661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3374T>C
AA Mutation p.Ile1125Thr(p.I1125T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25369613:25369613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375960766
CDS Mutation c.3496G>A
AA Mutation p.Glu1166Lys(p.E1166K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25342436:25342436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2546A>T
AA Mutation p.Asp849Val(p.D849V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25364691:25364691(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3110G>A
AA Mutation p.Ser1037Asn(p.S1037N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25401053:25401053(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4913G>T
AA Mutation p.Gly1638Val(p.G1638V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25410105:25410105(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773505640
CDS Mutation c.5411C>T
AA Mutation p.Pro1804Leu(p.P1804L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25342417:25342417(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2527T>G
AA Mutation p.Phe843Val(p.F843V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25382773:25382773(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4126C>A
AA Mutation p.Leu1376Ile(p.L1376I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25408878:25408878(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5342C>T
AA Mutation p.Ser1781Leu(p.S1781L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25317015:25317015(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1327C>T
AA Mutation p.Arg443Trp(p.R443W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25395690:25395690(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756518291
CDS Mutation c.4675G>A
AA Mutation p.Val1559Ile(p.V1559I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000276440
Start 25351741:25351741(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757392639
CDS Mutation c.2765C>T
AA Mutation p.Ala922Val(p.A922V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000276440
Start 25389219:25389219(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566691068
CDS Mutation c.4260G>A
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000276440
Start 25366911:25366911(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746243953
CDS Mutation c.3165C>T
Mutation Classification Silent
Feature Type Transcript
ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000276440
Start 25310420:25310420(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1206C>T
Mutation Classification Silent
Feature Type Transcript
ID 20
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000276440
Start 25399913:25399913(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4713delT
AA Mutation p.Phe1571LeufsTer19(p.F1571Lfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 21
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000276440
Start 25382674:25382674(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4033delA
AA Mutation p.Arg1345GlyfsTer12(p.R1345Gfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000276440
Start 25325373:25325373(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1735delA
AA Mutation p.Met579TrpfsTer8(p.M579Wfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000276440
Start 25395648:25395648(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4633delC
AA Mutation p.His1545ThrfsTer45(p.H1545Tfs*45)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 24
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000276440
Start 25292170:25292171(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.469dupA
AA Mutation p.Arg157LysfsTer12(p.R157Kfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 25
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000276440
Start 25395542:25395542(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4528-1G>A
Mutation Classification Splice_Site
Feature Type Transcript