ClinVar Miner

List of variants in gene RAB11A

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Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_004663.5(RAB11A):c.237-20A>G rs74845010 0.06152
NM_004663.5(RAB11A):c.265T>C (p.Leu89=) rs11556462 0.00242
NM_004663.5(RAB11A):c.591T>G (p.Pro197=) rs200883500 0.00063
NM_004663.5(RAB11A):c.511+19G>C rs368710927 0.00025
NM_004663.5(RAB11A):c.462G>A (p.Ser154=) rs372602014 0.00012
NM_004663.5(RAB11A):c.282T>A (p.Ala94=) rs746774499 0.00009
NM_004663.5(RAB11A):c.511+18A>C rs372655550 0.00009
NM_004663.5(RAB11A):c.511+20A>G rs377095606 0.00009
NM_004663.5(RAB11A):c.488C>G (p.Ala163Gly) rs201908439 0.00008
NM_004663.5(RAB11A):c.585G>A (p.Val195=) rs757949486 0.00005
NM_004663.5(RAB11A):c.384A>G (p.Leu128=) rs144399015 0.00003
NM_004663.5(RAB11A):c.438T>C (p.Asn146=) rs762066540 0.00003
NM_004663.5(RAB11A):c.650A>G (p.Ter217=) rs771181166 0.00003
NM_004663.5(RAB11A):c.216A>C (p.Arg72=) rs1037450547 0.00002
NM_004663.5(RAB11A):c.309G>A (p.Glu103=) rs769282556 0.00002
NM_004663.5(RAB11A):c.575G>A (p.Ser192Asn) rs778537719 0.00002
NC_000015.10:g.65867479G>C rs1446851303 0.00001
NM_004663.5(RAB11A):c.122A>G (p.Lys41Arg) rs2078196982 0.00001
NM_004663.5(RAB11A):c.12C>A (p.Arg4=) rs150316502 0.00001
NM_004663.5(RAB11A):c.165T>C (p.Val55=) rs759932662 0.00001
NM_004663.5(RAB11A):c.236+19A>C rs778892735 0.00001
NM_004663.5(RAB11A):c.236+7C>T rs757325109 0.00001
NM_004663.5(RAB11A):c.237-11T>C rs754167008 0.00001
NM_004663.5(RAB11A):c.272A>T (p.Tyr91Phe) rs190571382 0.00001
NM_004663.5(RAB11A):c.349A>G (p.Ile117Val) rs1190052210 0.00001
NM_004663.5(RAB11A):c.40+18C>G rs376773196 0.00001
NM_004663.5(RAB11A):c.41-14C>T rs2078196716 0.00001
NM_004663.5(RAB11A):c.41-19G>A rs928570862 0.00001
NM_004663.5(RAB11A):c.431-14G>A rs2078210195 0.00001
NM_004663.5(RAB11A):c.511+10G>A rs752472972 0.00001
NM_004663.5(RAB11A):c.521G>A (p.Arg174His) rs759435629 0.00001
NM_004663.5(RAB11A):c.555C>T (p.Arg185=) rs139295096 0.00001
NM_004663.5(RAB11A):c.581A>G (p.Asn194Ser) rs375723446 0.00001
NM_004663.5(RAB11A):c.69A>C (p.Gly23=) rs749827521 0.00001
NM_004663.5(RAB11A):c.90A>G (p.Arg30=) rs938576595 0.00001
NM_004663.5(RAB11A):c.97C>T (p.Arg33Ter) rs763409430 0.00001
NM_004663.5(RAB11A):c.104A>C (p.Glu35Ala) rs2549035433
NM_004663.5(RAB11A):c.104A>G (p.Glu35Gly)
NM_004663.5(RAB11A):c.10C>T (p.Arg4Cys) rs2141097983
NM_004663.5(RAB11A):c.127A>G (p.Thr43Ala) rs2549035437
NM_004663.5(RAB11A):c.129C>G (p.Thr43=) rs766878106
NM_004663.5(RAB11A):c.131T>C (p.Ile44Thr)
NM_004663.5(RAB11A):c.138A>C (p.Val46=) rs771254965
NM_004663.5(RAB11A):c.149C>T (p.Thr50Ile) rs2549035445
NM_004663.5(RAB11A):c.152G>C (p.Arg51Thr) rs1177010794
NM_004663.5(RAB11A):c.160C>T (p.Gln54Ter)
NM_004663.5(RAB11A):c.16G>C (p.Asp6His)
NM_004663.5(RAB11A):c.189G>A (p.Gln63=)
NM_004663.5(RAB11A):c.18C>G (p.Asp6Glu) rs2549033357
NM_004663.5(RAB11A):c.196G>T (p.Asp66Tyr)
NM_004663.5(RAB11A):c.200C>T (p.Thr67Ile) rs2549035453
NM_004663.5(RAB11A):c.201A>C (p.Thr67=) rs2078197191
NM_004663.5(RAB11A):c.210A>G (p.Gln70=) rs2141103499
NM_004663.5(RAB11A):c.236+14T>C rs1023620699
NM_004663.5(RAB11A):c.237-14G>C
NM_004663.5(RAB11A):c.237-3C>T rs2549035580
NM_004663.5(RAB11A):c.249A>G (p.Gly83=)
NM_004663.5(RAB11A):c.257G>T (p.Gly86Val)
NM_004663.5(RAB11A):c.291C>T (p.Leu97=) rs2549035598
NM_004663.5(RAB11A):c.294A>G (p.Thr98=) rs148440353
NM_004663.5(RAB11A):c.294A>T (p.Thr98=) rs148440353
NM_004663.5(RAB11A):c.29A>C (p.Tyr10Ser)
NM_004663.5(RAB11A):c.310C>T (p.Arg104Ter) rs2549035606
NM_004663.5(RAB11A):c.314G>C (p.Trp105Ser)
NM_004663.5(RAB11A):c.331G>A (p.Asp111Asn) rs1434404164
NM_004663.5(RAB11A):c.334C>A (p.His112Asn) rs2078198792
NM_004663.5(RAB11A):c.334C>G (p.His112Asp) rs2078198792
NM_004663.5(RAB11A):c.335A>G (p.His112Arg) rs772613563
NM_004663.5(RAB11A):c.33C>A (p.Leu11=) rs750861690
NM_004663.5(RAB11A):c.33C>T (p.Leu11=) rs750861690
NM_004663.5(RAB11A):c.363T>C (p.Leu121=) rs2141103762
NM_004663.5(RAB11A):c.375G>A (p.Lys125=) rs2141103767
NM_004663.5(RAB11A):c.378T>C (p.Ser126=)
NM_004663.5(RAB11A):c.388C>A (p.His130Asn)
NM_004663.5(RAB11A):c.410A>T (p.Asp137Val) rs2549035641
NM_004663.5(RAB11A):c.421G>A (p.Ala141Thr) rs2549035649
NM_004663.5(RAB11A):c.429A>C (p.Ala143=) rs2078199142
NM_004663.5(RAB11A):c.430+4A>G rs2549035655
NM_004663.5(RAB11A):c.430G>C (p.Glu144Gln) rs2549035654
NM_004663.5(RAB11A):c.431-12_431-11del
NM_004663.5(RAB11A):c.431-16T>C rs2141104954
NM_004663.5(RAB11A):c.431-5del rs759307551
NM_004663.5(RAB11A):c.431-6C>T rs776880248
NM_004663.5(RAB11A):c.431-8C>G
NM_004663.5(RAB11A):c.444G>A (p.Leu148=) rs2141104981
NM_004663.5(RAB11A):c.451A>G (p.Ile151Val) rs1292123777
NM_004663.5(RAB11A):c.452T>C (p.Ile151Thr)
NM_004663.5(RAB11A):c.456A>G (p.Glu152=) rs2078210405
NM_004663.5(RAB11A):c.461C>T (p.Ser154Leu) rs2549036281
NM_004663.5(RAB11A):c.500C>A (p.Thr167Lys) rs2549036302
NM_004663.5(RAB11A):c.502A>G (p.Ile168Val)
NM_004663.5(RAB11A):c.512-19G>T
NM_004663.5(RAB11A):c.512-20T>G rs770983297
NM_004663.5(RAB11A):c.517T>C (p.Tyr173His) rs2549038449
NM_004663.5(RAB11A):c.520C>T (p.Arg174Cys)
NM_004663.5(RAB11A):c.540A>C (p.Gln180His) rs2549038453
NM_004663.5(RAB11A):c.543G>A (p.Met181Ile)
NM_004663.5(RAB11A):c.553C>T (p.Arg185Cys) rs764020784
NM_004663.5(RAB11A):c.554G>A (p.Arg185His) rs2078263618
NM_004663.5(RAB11A):c.574A>C (p.Ser192Arg) rs2141110242
NM_004663.5(RAB11A):c.578A>G (p.Asn193Ser)
NM_004663.5(RAB11A):c.598G>A (p.Val200Ile) rs1015728032
NM_004663.5(RAB11A):c.610A>G (p.Thr204Ala) rs1280621310
NM_004663.5(RAB11A):c.617A>G (p.Asn206Ser) rs770049340
NM_004663.5(RAB11A):c.624A>C (p.Pro208=) rs2549038501

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