ClinVar Miner

List of variants in gene VPS13B reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 113
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HGVS dbSNP
NM_015243.2(VPS13B):c.1041A>G (p.Ser347=) rs149176010
NM_015243.2(VPS13B):c.1108G>C (p.Asp370His) rs748531719
NM_015243.2(VPS13B):c.1289G>C (p.Gly430Ala) rs147448147
NM_015243.2(VPS13B):c.1463C>T (p.Thr488Met) rs150783688
NM_015243.2(VPS13B):c.1559A>G (p.His520Arg) rs143205296
NM_015243.2(VPS13B):c.1646G>A (p.Gly549Asp) rs886062536
NM_015243.2(VPS13B):c.1700G>A (p.Gly567Glu) rs141046414
NM_015243.2(VPS13B):c.1832G>A (p.Arg611Lys) rs61754109
NM_015243.2(VPS13B):c.1843+10T>C rs371154826
NM_015243.2(VPS13B):c.1864A>G (p.Thr622Ala) rs398124329
NM_015243.2(VPS13B):c.1954A>C (p.Ile652Leu) rs886062537
NM_015243.2(VPS13B):c.211T>C (p.Trp71Arg) rs886062534
NM_015243.2(VPS13B):c.2451T>C (p.His817=) rs114120664
NM_015243.2(VPS13B):c.358A>G (p.Ile120Val) rs201147123
NM_015243.2(VPS13B):c.365C>T (p.Pro122Leu) rs201723380
NM_015243.2(VPS13B):c.406C>T (p.Pro136Ser) rs757950339
NM_015243.2(VPS13B):c.56A>G (p.Lys19Arg) rs200327756
NM_015243.2(VPS13B):c.584C>G (p.Thr195Ser) rs770738729
NM_015243.2(VPS13B):c.886G>A (p.Glu296Lys) rs886062535
NM_017890.4(VPS13B):c.*1105_*1108dupTGAT rs543048641
NM_017890.4(VPS13B):c.*1106_*1108dupGAT rs765534822
NM_017890.4(VPS13B):c.*1207G>C rs182082022
NM_017890.4(VPS13B):c.*1345C>T rs778566330
NM_017890.4(VPS13B):c.*1355T>G rs562826355
NM_017890.4(VPS13B):c.*140G>A rs535987441
NM_017890.4(VPS13B):c.*1483C>A rs886062558
NM_017890.4(VPS13B):c.*1504_*1507dupCTTT rs747583708
NM_017890.4(VPS13B):c.*1540T>C rs148026916
NM_017890.4(VPS13B):c.*202T>A rs201566966
NM_017890.4(VPS13B):c.*270C>T rs886062550
NM_017890.4(VPS13B):c.*305G>A rs149912942
NM_017890.4(VPS13B):c.*705T>C rs886062554
NM_017890.4(VPS13B):c.*733A>T rs886062555
NM_017890.4(VPS13B):c.*740G>C rs886062556
NM_017890.4(VPS13B):c.*743T>G rs144603951
NM_017890.4(VPS13B):c.10018G>A (p.Val3340Ile) rs116746734
NM_017890.4(VPS13B):c.10018G>T (p.Val3340Phe) rs116746734
NM_017890.4(VPS13B):c.10086C>G (p.Ile3362Met) rs542986432
NM_017890.4(VPS13B):c.10124C>T (p.Thr3375Ile) rs138127778
NM_017890.4(VPS13B):c.10175C>A (p.Thr3392Asn) rs759636784
NM_017890.4(VPS13B):c.10459C>T (p.Leu3487Phe) rs761972356
NM_017890.4(VPS13B):c.10501T>C (p.Cys3501Arg) rs886062549
NM_017890.4(VPS13B):c.10620C>A (p.Tyr3540Ter) rs758842658
NM_017890.4(VPS13B):c.10640C>T (p.Thr3547Ile) rs781253026
NM_017890.4(VPS13B):c.10643A>G (p.Tyr3548Cys) rs398124326
NM_017890.4(VPS13B):c.10830C>T (p.Asp3610=) rs145950999
NM_017890.4(VPS13B):c.11007C>T (p.Asn3669=) rs745337140
NM_017890.4(VPS13B):c.11146G>A (p.Ala3716Thr) rs142476821
NM_017890.4(VPS13B):c.11162G>A (p.Arg3721Gln) rs757726642
NM_017890.4(VPS13B):c.11270G>A (p.Arg3757Gln) rs149318176
NM_017890.4(VPS13B):c.11413G>T (p.Val3805Leu) rs138565077
NM_017890.4(VPS13B):c.11688C>T (p.Phe3896=) rs139436386
NM_017890.4(VPS13B):c.11834G>A (p.Arg3945Gln) rs147907236
NM_017890.4(VPS13B):c.11862C>T (p.Asn3954=) rs147710096
NM_017890.4(VPS13B):c.11959C>G (p.Pro3987Ala) rs201483764
NM_017890.4(VPS13B):c.11972A>T (p.Lys3991Ile) rs117934093
NM_017890.4(VPS13B):c.2583C>T (p.Cys861=) rs199868590
NM_017890.4(VPS13B):c.2596G>A (p.Val866Ile) rs150185067
NM_017890.4(VPS13B):c.2643A>T (p.Lys881Asn) rs148777544
NM_017890.4(VPS13B):c.2651-12A>G rs886062538
NM_017890.4(VPS13B):c.2704A>G (p.Lys902Glu) rs149531438
NM_017890.4(VPS13B):c.2752T>C (p.Ser918Pro) rs886062539
NM_017890.4(VPS13B):c.2760A>G (p.Leu920=) rs138661755
NM_017890.4(VPS13B):c.2823C>T (p.Ser941=) rs199881514
NM_017890.4(VPS13B):c.2830G>T (p.Val944Leu) rs753607562
NM_017890.4(VPS13B):c.3075G>A (p.Thr1025=) rs141637316
NM_017890.4(VPS13B):c.3083-9C>T rs376659281
NM_017890.4(VPS13B):c.3211-11T>C rs77129176
NM_017890.4(VPS13B):c.3240del (p.Pro1081fs) rs764544747
NM_017890.4(VPS13B):c.3243A>G (p.Pro1081=) rs34961653
NM_017890.4(VPS13B):c.3297A>C (p.Thr1099=) rs200982547
NM_017890.4(VPS13B):c.3363A>G (p.Ile1121Met) rs191099208
NM_017890.4(VPS13B):c.3436C>G (p.Leu1146Val) rs202015701
NM_017890.4(VPS13B):c.3667-5C>G rs886062540
NM_017890.4(VPS13B):c.3751A>G (p.Thr1251Ala) rs184693266
NM_017890.4(VPS13B):c.3813A>G (p.Thr1271=) rs775071483
NM_017890.4(VPS13B):c.3865A>G (p.Thr1289Ala) rs752808333
NM_017890.4(VPS13B):c.4300-6G>A rs199755508
NM_017890.4(VPS13B):c.4337A>G (p.His1446Arg) rs371961155
NM_017890.4(VPS13B):c.4626C>G (p.Arg1542=) rs150376603
NM_017890.4(VPS13B):c.4762A>G (p.Met1588Val) rs886062541
NM_017890.4(VPS13B):c.4821-7T>C rs201136777
NM_017890.4(VPS13B):c.4936C>T (p.Pro1646Ser) rs563705133
NM_017890.4(VPS13B):c.5168G>T (p.Gly1723Val) rs368362777
NM_017890.4(VPS13B):c.5344G>A (p.Ala1782Thr) rs146540735
NM_017890.4(VPS13B):c.5471G>A (p.Arg1824His) rs755227174
NM_017890.4(VPS13B):c.5647G>A (p.Asp1883Asn) rs886062542
NM_017890.4(VPS13B):c.5738T>C (p.Ile1913Thr) rs779082817
NM_017890.4(VPS13B):c.5816G>A (p.Arg1939Gln) rs150272676
NM_017890.4(VPS13B):c.5890T>G (p.Leu1964Val) rs751559027
NM_017890.4(VPS13B):c.5983+14A>C rs886062543
NM_017890.4(VPS13B):c.6751C>T (p.His2251Tyr) rs747340772
NM_017890.4(VPS13B):c.7126-1G>A rs930144563
NM_017890.4(VPS13B):c.7163A>G (p.Lys2388Arg) rs778935189
NM_017890.4(VPS13B):c.7441G>A (p.Val2481Ile) rs201963516
NM_017890.4(VPS13B):c.7750G>T (p.Val2584Leu) rs144668374
NM_017890.4(VPS13B):c.7787C>T (p.Ser2596Phe) rs145208175
NM_017890.4(VPS13B):c.7955A>C (p.Asn2652Thr) rs886062544
NM_017890.4(VPS13B):c.7997G>A (p.Arg2666His) rs398124338
NM_017890.4(VPS13B):c.8246A>G (p.Tyr2749Cys) rs138453594
NM_017890.4(VPS13B):c.8356G>T (p.Val2786Leu) rs886062545
NM_017890.4(VPS13B):c.8436+12C>T rs886062546
NM_017890.4(VPS13B):c.8645C>T (p.Pro2882Leu) rs145890213
NM_017890.4(VPS13B):c.8868-7G>A rs886062547
NM_017890.4(VPS13B):c.9175G>A (p.Gly3059Ser) rs778256097
NM_017890.4(VPS13B):c.9342T>C (p.Asn3114=) rs886062548
NM_017890.4(VPS13B):c.9414T>A (p.Arg3138=) rs78277780
NM_017890.4(VPS13B):c.9444C>T (p.Cys3148=) rs745668942
NM_017890.4(VPS13B):c.9605T>C (p.Leu3202Pro) rs199559979
NM_017890.4(VPS13B):c.9658G>A (p.Gly3220Arg) rs772658121
NM_017890.4(VPS13B):c.9678A>G (p.Gly3226=) rs564362618
NM_017890.4(VPS13B):c.9859G>A (p.Glu3287Lys) rs756531043
NM_017890.4(VPS13B):c.9906G>A (p.Pro3302=) rs775601813

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