ClinVar Miner

List of variants in gene MBD5 reported as uncertain significance by Invitae

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Total variants: 112
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HGVS dbSNP
NC_000002.11:g.(?_149216308)_(149270530_?)dup
NM_018328.4(MBD5):c.1041G>T (p.Gln347His) rs746751148
NM_018328.4(MBD5):c.1141T>C (p.Phe381Leu) rs768570356
NM_018328.4(MBD5):c.1198G>A (p.Val400Ile) rs377568191
NM_018328.4(MBD5):c.1234G>A (p.Val412Ile) rs761118931
NM_018328.4(MBD5):c.1249A>G (p.Met417Val)
NM_018328.4(MBD5):c.1304C>T (p.Ser435Phe) rs768225923
NM_018328.4(MBD5):c.1327G>A (p.Val443Met) rs137977565
NM_018328.4(MBD5):c.1327G>T (p.Val443Leu) rs137977565
NM_018328.4(MBD5):c.1372C>A (p.Gln458Lys)
NM_018328.4(MBD5):c.1510A>G (p.Met504Val) rs114251920
NM_018328.4(MBD5):c.1535C>T (p.Ser512Phe) rs201695275
NM_018328.4(MBD5):c.1564C>T (p.Pro522Ser) rs1161083244
NM_018328.4(MBD5):c.156A>G (p.Thr52=) rs796958008
NM_018328.4(MBD5):c.1570C>T (p.Pro524Ser) rs727503998
NM_018328.4(MBD5):c.1634C>G (p.Ser545Cys) rs1553518618
NM_018328.4(MBD5):c.1842_1865del (p.Glu615_Thr622del) rs780715275
NM_018328.4(MBD5):c.1987C>T (p.Pro663Ser) rs1057520996
NM_018328.4(MBD5):c.19T>A (p.Cys7Ser) rs766104877
NM_018328.4(MBD5):c.19T>C (p.Cys7Arg)
NM_018328.4(MBD5):c.2011A>G (p.Arg671Gly) rs1376331579
NM_018328.4(MBD5):c.2108A>G (p.Gln703Arg) rs1553518707
NM_018328.4(MBD5):c.2162C>T (p.Pro721Leu) rs138639760
NM_018328.4(MBD5):c.2198C>T (p.Ser733Phe) rs1438163020
NM_018328.4(MBD5):c.2240G>C (p.Ser747Thr)
NM_018328.4(MBD5):c.2257C>A (p.Pro753Thr) rs370340010
NM_018328.4(MBD5):c.2275G>A (p.Val759Met) rs377604964
NM_018328.4(MBD5):c.2278C>T (p.His760Tyr) rs1060501150
NM_018328.4(MBD5):c.2279A>G (p.His760Arg) rs763275881
NM_018328.4(MBD5):c.2314A>C (p.Asn772His) rs200151142
NM_018328.4(MBD5):c.2358G>T (p.Gln786His)
NM_018328.4(MBD5):c.2384T>A (p.Met795Lys) rs1446479503
NM_018328.4(MBD5):c.2402T>C (p.Met801Thr)
NM_018328.4(MBD5):c.2426C>G (p.Pro809Arg) rs1060501152
NM_018328.4(MBD5):c.247A>G (p.Lys83Glu) rs1559083055
NM_018328.4(MBD5):c.2495A>G (p.Tyr832Cys) rs954814725
NM_018328.4(MBD5):c.2502A>C (p.Gln834His) rs147272790
NM_018328.4(MBD5):c.2521G>A (p.Gly841Ser)
NM_018328.4(MBD5):c.2530C>T (p.Pro844Ser)
NM_018328.4(MBD5):c.2543T>G (p.Ile848Arg)
NM_018328.4(MBD5):c.2552C>T (p.Ala851Val)
NM_018328.4(MBD5):c.25G>C (p.Gly9Arg)
NM_018328.4(MBD5):c.2621C>A (p.Ala874Glu)
NM_018328.4(MBD5):c.268G>A (p.Val90Ile) rs1329667912
NM_018328.4(MBD5):c.2724C>G (p.Asn908Lys)
NM_018328.4(MBD5):c.274G>A (p.Ala92Thr) rs770801894
NM_018328.4(MBD5):c.2750G>A (p.Ser917Asn)
NM_018328.4(MBD5):c.2751C>G (p.Ser917Arg)
NM_018328.4(MBD5):c.2789A>C (p.Gln930Pro) rs564759063
NM_018328.4(MBD5):c.2865C>A (p.Asn955Lys) rs1559096615
NM_018328.4(MBD5):c.2884C>A (p.Gln962Lys) rs1200329763
NM_018328.4(MBD5):c.2891C>T (p.Thr964Ile)
NM_018328.4(MBD5):c.2903C>T (p.Ser968Leu) rs200985982
NM_018328.4(MBD5):c.2978A>C (p.Gln993Pro) rs761395486
NM_018328.4(MBD5):c.2979G>C (p.Gln993His) rs148321416
NM_018328.4(MBD5):c.302T>C (p.Ile101Thr) rs1559083106
NM_018328.4(MBD5):c.3035G>A (p.Cys1012Tyr) rs1559096858
NM_018328.4(MBD5):c.3063G>A (p.Met1021Ile)
NM_018328.4(MBD5):c.3067G>A (p.Glu1023Lys) rs1064796473
NM_018328.4(MBD5):c.3073G>T (p.Ala1025Ser) rs1553520432
NM_018328.4(MBD5):c.3087C>G (p.Asn1029Lys) rs771343592
NM_018328.4(MBD5):c.3094A>G (p.Ile1032Val)
NM_018328.4(MBD5):c.3094A>T (p.Ile1032Leu) rs774513612
NM_018328.4(MBD5):c.3104A>C (p.Gln1035Pro) rs1559098476
NM_018328.4(MBD5):c.3182C>T (p.Pro1061Leu) rs375158010
NM_018328.4(MBD5):c.321T>G (p.Ile107Met) rs1553517962
NM_018328.4(MBD5):c.3253G>A (p.Val1085Ile) rs199626531
NM_018328.4(MBD5):c.3266A>G (p.Tyr1089Cys) rs1234231456
NM_018328.4(MBD5):c.3355G>T (p.Ala1119Ser) rs373177231
NM_018328.4(MBD5):c.3385T>C (p.Ser1129Pro) rs200395037
NM_018328.4(MBD5):c.3389T>C (p.Ile1130Thr) rs748142226
NM_018328.4(MBD5):c.3407T>C (p.Leu1136Pro)
NM_018328.4(MBD5):c.3436G>C (p.Gly1146Arg) rs1559098890
NM_018328.4(MBD5):c.3440G>A (p.Arg1147Gln) rs368605084
NM_018328.4(MBD5):c.3494G>A (p.Arg1165Gln) rs727503999
NM_018328.4(MBD5):c.3500C>T (p.Pro1167Leu) rs1057522316
NM_018328.4(MBD5):c.3539A>T (p.Asp1180Val) rs752035001
NM_018328.4(MBD5):c.3614G>T (p.Gly1205Val) rs1559099144
NM_018328.4(MBD5):c.3623A>G (p.Asn1208Ser)
NM_018328.4(MBD5):c.3739A>G (p.Ile1247Val) rs746105686
NM_018328.4(MBD5):c.3768G>T (p.Gly1256=)
NM_018328.4(MBD5):c.3808A>G (p.Lys1270Glu)
NM_018328.4(MBD5):c.3820A>G (p.Met1274Val)
NM_018328.4(MBD5):c.385G>A (p.Gly129Arg)
NM_018328.4(MBD5):c.3902T>C (p.Phe1301Ser) rs755983540
NM_018328.4(MBD5):c.3993A>C (p.Lys1331Asn) rs1553520621
NM_018328.4(MBD5):c.4033G>A (p.Val1345Ile) rs376249586
NM_018328.4(MBD5):c.4042T>C (p.Cys1348Arg) rs1396512077
NM_018328.4(MBD5):c.4159G>A (p.Asp1387Asn) rs750381367
NM_018328.4(MBD5):c.4221C>A (p.Asp1407Glu)
NM_018328.4(MBD5):c.4439G>A (p.Arg1480Lys)
NM_018328.4(MBD5):c.46C>A (p.Leu16Ile) rs749436847
NM_018328.4(MBD5):c.502T>C (p.Phe168Leu) rs1225184691
NM_018328.4(MBD5):c.55A>G (p.Ile19Val) rs1559080667
NM_018328.4(MBD5):c.599G>A (p.Arg200Gln) rs149278000
NM_018328.4(MBD5):c.606A>T (p.Arg202Ser) rs1553518446
NM_018328.4(MBD5):c.622C>T (p.His208Tyr)
NM_018328.4(MBD5):c.644G>A (p.Arg215His) rs771325235
NM_018328.4(MBD5):c.69G>A (p.Val23=) rs151204004
NM_018328.4(MBD5):c.718A>G (p.Arg240Gly) rs767317924
NM_018328.4(MBD5):c.742G>C (p.Asp248His)
NM_018328.4(MBD5):c.763C>T (p.Pro255Ser) rs183855575
NM_018328.4(MBD5):c.796A>G (p.Ile266Val) rs568826753
NM_018328.4(MBD5):c.811A>G (p.Thr271Ala)
NM_018328.4(MBD5):c.826C>T (p.Pro276Ser) rs376756158
NM_018328.4(MBD5):c.869C>G (p.Ala290Gly) rs1559085941
NM_018328.4(MBD5):c.884C>G (p.Thr295Ser) rs368339420
NM_018328.4(MBD5):c.887A>G (p.Asn296Ser)
NM_018328.4(MBD5):c.935A>T (p.Lys312Ile) rs146031838
NM_018328.4(MBD5):c.936A>C (p.Lys312Asn)
NM_018328.4(MBD5):c.961A>G (p.Met321Val) rs369869865
NM_018328.4(MBD5):c.980T>C (p.Met327Thr) rs776228346

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