Primary Site >> Stomach Cancer

Gene >> SLITRK5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676386:87676386(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.998G>A
AA Mutation p.Gly333Glu(p.G333E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676578:87676578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1190A>C
AA Mutation p.Lys397Thr(p.K397T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677883:87677883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2495C>T
AA Mutation p.Ala832Val(p.A832V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677312:87677312(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745820982
CDS Mutation c.1924C>T
AA Mutation p.Arg642Trp(p.R642W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676396:87676396(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1008A>C
AA Mutation p.Gln336His(p.Q336H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676531:87676531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1143C>A
AA Mutation p.Asn381Lys(p.N381K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676397:87676397(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1009C>A
AA Mutation p.Pro337Thr(p.P337T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676020:87676020(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.632G>T
AA Mutation p.Arg211Leu(p.R211L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677474:87677474(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774581110
CDS Mutation c.2086C>A
AA Mutation p.Gln696Lys(p.Q696K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87678078:87678078(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2690G>A
AA Mutation p.Arg897His(p.R897H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87675791:87675791(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.403C>A
AA Mutation p.His135Asn(p.H135N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676400:87676400(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1012A>G
AA Mutation p.Asn338Asp(p.N338D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87675764:87675764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.376C>A
AA Mutation p.His126Asn(p.H126N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676415:87676415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1027C>T
AA Mutation p.Arg343Cys(p.R343C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676932:87676932(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1544A>G
AA Mutation p.Asn515Ser(p.N515S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676785:87676785(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1397G>A
AA Mutation p.Gly466Asp(p.G466D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677183:87677183(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1795G>A
AA Mutation p.Ala599Thr(p.A599T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676583:87676583(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758176397
CDS Mutation c.1195G>A
AA Mutation p.Glu399Lys(p.E399K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677144:87677144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1756C>A
AA Mutation p.Leu586Ile(p.L586I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676130:87676130(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.742G>T
AA Mutation p.Asp248Tyr(p.D248Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676748:87676748(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1360G>A
AA Mutation p.Gly454Arg(p.G454R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677444:87677444(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754772123
CDS Mutation c.2056G>C
AA Mutation p.Val686Leu(p.V686L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677378:87677378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1990T>C
AA Mutation p.Ser664Pro(p.S664P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677574:87677574(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2186C>T
AA Mutation p.Ala729Val(p.A729V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87678123:87678123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2735G>A
AA Mutation p.Arg912Gln(p.R912Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676167:87676167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.779G>T
AA Mutation p.Gly260Val(p.G260V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677181:87677181(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1793T>A
AA Mutation p.Phe598Tyr(p.F598Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677490:87677490(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2102G>A
AA Mutation p.Ser701Asn(p.S701N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677364:87677364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1976C>T
AA Mutation p.Ser659Leu(p.S659L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676194:87676194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.806G>A
AA Mutation p.Arg269His(p.R269H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87676566:87676566(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1178G>T
AA Mutation p.Cys393Phe(p.C393F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677543:87677543(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2155G>A
AA Mutation p.Gly719Ser(p.G719S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677714:87677714(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2326T>C
AA Mutation p.Tyr776His(p.Y776H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87678041:87678041(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2653G>A
AA Mutation p.Ala885Thr(p.A885T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87678218:87678218(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2830G>A
AA Mutation p.Asp944Asn(p.D944N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000325089
Start 87677696:87677696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2308G>T
AA Mutation p.Gly770Cys(p.G770C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676828:87676828(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1440G>A
Mutation Classification Silent
Feature Type Transcript
ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676162:87676162(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.774G>C
Mutation Classification Silent
Feature Type Transcript
ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677254:87677254(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775241600
CDS Mutation c.1866G>A
Mutation Classification Silent
Feature Type Transcript
ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676429:87676429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1041G>A
Mutation Classification Silent
Feature Type Transcript
ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677326:87677326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1938C>T
Mutation Classification Silent
Feature Type Transcript
ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676741:87676741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1353C>T
Mutation Classification Silent
Feature Type Transcript
ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677182:87677182(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs555137445
CDS Mutation c.1794C>T
Mutation Classification Silent
Feature Type Transcript
ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677827:87677827(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2439G>C
Mutation Classification Silent
Feature Type Transcript
ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676426:87676426(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1038T>C
Mutation Classification Silent
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676498:87676498(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1110G>A
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87675457:87675457(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762869284
CDS Mutation c.69G>A
Mutation Classification Silent
Feature Type Transcript
ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676867:87676867(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777152769
CDS Mutation c.1479C>T
Mutation Classification Silent
Feature Type Transcript
ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677383:87677383(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1995G>T
Mutation Classification Silent
Feature Type Transcript
ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87678013:87678013(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757141870
CDS Mutation c.2625G>A
Mutation Classification Silent
Feature Type Transcript
ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676672:87676672(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1284C>T
Mutation Classification Silent
Feature Type Transcript
ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87678217:87678217(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771423229
CDS Mutation c.2829G>A
Mutation Classification Silent
Feature Type Transcript
ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676651:87676651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1263C>T
Mutation Classification Silent
Feature Type Transcript
ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87675655:87675655(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.267C>T
Mutation Classification Silent
Feature Type Transcript
ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87675529:87675529(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.141C>T
Mutation Classification Silent
Feature Type Transcript
ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677788:87677788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2400G>A
Mutation Classification Silent
Feature Type Transcript
ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87675535:87675535(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758620361
CDS Mutation c.147C>T
Mutation Classification Silent
Feature Type Transcript
ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677659:87677659(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2271C>T
Mutation Classification Silent
Feature Type Transcript
ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677368:87677368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1980G>A
Mutation Classification Silent
Feature Type Transcript
ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677200:87677200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1812C>A
Mutation Classification Silent
Feature Type Transcript
ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87677620:87677620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2232C>T
Mutation Classification Silent
Feature Type Transcript
ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000325089
Start 87676582:87676582(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1194C>A
Mutation Classification Silent
Feature Type Transcript
ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000325089
Start 87678142:87678142(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2759delC
AA Mutation p.Pro920ArgfsTer6(p.P920Rfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000325089
Start 87677331:87677331(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1947delC
AA Mutation p.Ala650ArgfsTer17(p.A650Rfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000325089
Start 87678100:87678100(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2716delG
AA Mutation p.Ala906GlnfsTer20(p.A906Qfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000325089
Start 87677327:87677327(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1942delG
AA Mutation p.Ala648ProfsTer19(p.A648Pfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 67
Mutation Consequence frameshift_variant
Transcription ID ENST00000325089
Start 87677532:87677580(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2146_2194delGTGTACGGCGGCGGCGGCGGCACGGGCGGCCACCCACACGCGCACGTGC
AA Mutation p.Val716IlefsTer10(p.V716Ifs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 68
Mutation Consequence stop_gained
Transcription ID ENST00000325089
Start 87678200:87678200(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2812A>T
AA Mutation p.Lys938Ter(p.K938*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 69
Mutation Consequence stop_gained
Transcription ID ENST00000325089
Start 87678188:87678188(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2800G>T
AA Mutation p.Glu934Ter(p.E934*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 70
Mutation Consequence stop_gained
Transcription ID ENST00000325089
Start 87676648:87676648(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1260C>A
AA Mutation p.Tyr420Ter(p.Y420*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 71
Mutation Consequence stop_gained
Transcription ID ENST00000325089
Start 87677807:87677807(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2419C>T
AA Mutation p.Gln807Ter(p.Q807*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript