ClinVar Miner

List of variants in gene DYNC2H1 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_001377.3(DYNC2H1):c.11263A>G (p.Met3755Val) rs137853026 0.00105
NM_001377.3(DYNC2H1):c.6551A>T (p.Asp2184Val) rs201967064 0.00101
NM_001377.3(DYNC2H1):c.6047A>G (p.Tyr2016Cys) rs200190291 0.00090
NM_001377.3(DYNC2H1):c.3170G>A (p.Arg1057His) rs191381310 0.00069
NM_001377.3(DYNC2H1):c.1288C>T (p.Arg430Cys) rs374073337 0.00053
NM_001377.3(DYNC2H1):c.1774C>T (p.Leu592Phe) rs180861816 0.00052
NM_001377.3(DYNC2H1):c.6093T>G (p.Asp2031Glu) rs372641908 0.00047
NM_001377.3(DYNC2H1):c.12082G>T (p.Gly4028Cys) rs202216852 0.00044
NM_001377.3(DYNC2H1):c.317G>A (p.Ser106Asn) rs200485999 0.00042
NM_001377.3(DYNC2H1):c.3419G>T (p.Gly1140Val) rs201043335 0.00042
NM_001377.3(DYNC2H1):c.6625A>T (p.Thr2209Ser) rs200762072 0.00041
NM_001377.3(DYNC2H1):c.10883C>T (p.Thr3628Ile) rs1057524234 0.00034
NM_001377.3(DYNC2H1):c.5473A>G (p.Ile1825Val) rs201860217 0.00029
NM_001377.3(DYNC2H1):c.4916C>A (p.Thr1639Lys) rs200239560 0.00026
NM_001377.3(DYNC2H1):c.2194G>A (p.Val732Ile) rs370906388 0.00019
NM_001377.3(DYNC2H1):c.7967G>A (p.Arg2656His) rs200614421 0.00018
NM_001377.3(DYNC2H1):c.1157C>T (p.Ser386Phe) rs541038013 0.00016
NM_001377.3(DYNC2H1):c.12376G>A (p.Ala4126Thr) rs200636241 0.00016
NM_001377.3(DYNC2H1):c.3607G>A (p.Glu1203Lys) rs202051528 0.00015
NM_001377.3(DYNC2H1):c.9242G>A (p.Arg3081His) rs749753983 0.00015
NM_001377.3(DYNC2H1):c.11176A>G (p.Ile3726Val) rs370622418 0.00014
NM_001377.3(DYNC2H1):c.11788C>T (p.Arg3930Cys) rs199705540 0.00014
NM_001377.3(DYNC2H1):c.12040G>A (p.Val4014Ile) rs532644983 0.00014
NM_001377.3(DYNC2H1):c.11726G>A (p.Gly3909Asp) rs201479015 0.00013
NM_001377.3(DYNC2H1):c.12776G>T (p.Gly4259Val) rs368203507 0.00013
NM_001377.3(DYNC2H1):c.10550G>A (p.Arg3517His) rs188113889 0.00012
NM_001377.3(DYNC2H1):c.6697T>C (p.Ser2233Pro) rs375988913 0.00012
NM_001377.3(DYNC2H1):c.5960C>T (p.Thr1987Met) rs769618486 0.00011
NM_001377.3(DYNC2H1):c.8782A>C (p.Lys2928Gln) rs190819700 0.00010
NM_001377.3(DYNC2H1):c.12025A>C (p.Met4009Leu) rs763169398 0.00009
NM_001377.3(DYNC2H1):c.12833A>T (p.Asp4278Val) rs200268681 0.00009
NM_001377.3(DYNC2H1):c.7597C>T (p.Arg2533Cys) rs754889986 0.00008
NM_001377.3(DYNC2H1):c.5821G>C (p.Ala1941Pro) rs368058473 0.00006
NM_001377.3(DYNC2H1):c.10277A>C (p.Glu3426Ala) rs375512191 0.00004
NM_001377.3(DYNC2H1):c.4900A>G (p.Met1634Val) rs753296481 0.00004
NM_001377.3(DYNC2H1):c.9011G>A (p.Arg3004His) rs755871858 0.00004
NM_001377.3(DYNC2H1):c.9262C>T (p.Pro3088Ser) rs764931443 0.00004
NM_001377.3(DYNC2H1):c.11858T>C (p.Ile3953Thr) rs769616176 0.00003
NM_001377.3(DYNC2H1):c.12439C>T (p.Arg4147Cys) rs755441612 0.00003
NM_001377.3(DYNC2H1):c.3110A>T (p.Lys1037Ile) rs768433759 0.00003
NM_001377.3(DYNC2H1):c.8536T>C (p.Ser2846Pro) rs767717747 0.00003
NM_001377.3(DYNC2H1):c.10805G>A (p.Arg3602Gln) rs1263873884 0.00002
NM_001377.3(DYNC2H1):c.5060C>T (p.Pro1687Leu) rs376385873 0.00002
NM_001377.3(DYNC2H1):c.7277G>T (p.Arg2426Leu) rs373521030 0.00002
NM_001377.3(DYNC2H1):c.9037A>C (p.Ile3013Leu) rs1250296341 0.00002
NM_001377.3(DYNC2H1):c.998A>C (p.Glu333Ala) rs763366904 0.00002
NM_001377.3(DYNC2H1):c.10664T>C (p.Val3555Ala) rs1555082969 0.00001
NM_001377.3(DYNC2H1):c.10844C>T (p.Pro3615Leu) rs1468117934 0.00001
NM_001377.3(DYNC2H1):c.11629A>G (p.Arg3877Gly) rs1194851950 0.00001
NM_001377.3(DYNC2H1):c.12317T>C (p.Leu4106Ser) rs369591902 0.00001
NM_001377.3(DYNC2H1):c.5719A>G (p.Met1907Val) rs748735826 0.00001
NM_001377.3(DYNC2H1):c.11021A>G (p.Gln3674Arg) rs2135353472
NM_001377.3(DYNC2H1):c.11324A>G (p.Asp3775Gly)
NM_001377.3(DYNC2H1):c.11429C>G (p.Thr3810Ser) rs1555096677
NM_001377.3(DYNC2H1):c.11705T>C (p.Ile3902Thr)
NM_001377.3(DYNC2H1):c.11977C>A (p.Pro3993Thr) rs1275865339
NM_001377.3(DYNC2H1):c.12589A>G (p.Ser4197Gly) rs1466748798
NM_001377.3(DYNC2H1):c.12916A>C (p.Asn4306His) rs200264343
NM_001377.3(DYNC2H1):c.1516C>T (p.Leu506Phe)
NM_001377.3(DYNC2H1):c.1760G>T (p.Arg587Leu) rs1238414767
NM_001377.3(DYNC2H1):c.1953G>A (p.Lys651=) rs1178331074
NM_001377.3(DYNC2H1):c.2183G>A (p.Gly728Asp)
NM_001377.3(DYNC2H1):c.2289G>C (p.Met763Ile) rs1057524436
NM_001377.3(DYNC2H1):c.2717A>G (p.Asp906Gly) rs949692251
NM_001377.3(DYNC2H1):c.2987T>G (p.Leu996Arg)
NM_001377.3(DYNC2H1):c.3190G>A (p.Gly1064Ser)
NM_001377.3(DYNC2H1):c.3794G>A (p.Arg1265His) rs200635842
NM_001377.3(DYNC2H1):c.4069G>C (p.Gly1357Arg) rs745380950
NM_001377.3(DYNC2H1):c.4349T>C (p.Ile1450Thr)
NM_001377.3(DYNC2H1):c.4442G>A (p.Gly1481Glu) rs2134918675
NM_001377.3(DYNC2H1):c.4916C>T (p.Thr1639Ile) rs200239560
NM_001377.3(DYNC2H1):c.5129T>A (p.Val1710Asp) rs777396565
NM_001377.3(DYNC2H1):c.5189G>A (p.Gly1730Asp) rs1280509051
NM_001377.3(DYNC2H1):c.5389G>A (p.Gly1797Ser) rs1064796293
NM_001377.3(DYNC2H1):c.5492A>G (p.Tyr1831Cys)
NM_001377.3(DYNC2H1):c.554G>A (p.Arg185His) rs199960819
NM_001377.3(DYNC2H1):c.5930T>C (p.Ile1977Thr) rs2134994345
NM_001377.3(DYNC2H1):c.6019A>G (p.Thr2007Ala) rs1064796480
NM_001377.3(DYNC2H1):c.6348-31A>G
NM_001377.3(DYNC2H1):c.6962A>G (p.Gln2321Arg)
NM_001377.3(DYNC2H1):c.7414T>A (p.Ser2472Thr) rs752287365
NM_001377.3(DYNC2H1):c.9391G>C (p.Glu3131Gln) rs983700534

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