ClinVar Miner

List of variants in gene SNRNP200 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_014014.5(SNRNP200):c.*61T>C rs571136350 0.00130
NM_014014.5(SNRNP200):c.*331G>C rs557818805 0.00073
NM_014014.5(SNRNP200):c.574+9G>A rs145559167 0.00045
NM_014014.5(SNRNP200):c.3640-15T>C rs200824314 0.00036
NM_014014.5(SNRNP200):c.4448G>A (p.Arg1483Gln) rs779888644 0.00032
NM_014014.5(SNRNP200):c.2928G>A (p.Thr976=) rs375734152 0.00026
NM_014014.5(SNRNP200):c.578A>G (p.Asp193Gly) rs144423660 0.00024
NM_014014.5(SNRNP200):c.2665A>G (p.Ile889Val) rs140087655 0.00023
NM_014014.5(SNRNP200):c.46-7T>C rs373701482 0.00022
NM_014014.5(SNRNP200):c.2122G>A (p.Val708Ile) rs191245006 0.00019
NM_014014.5(SNRNP200):c.4678A>G (p.Ile1560Val) rs78715863 0.00018
NM_014014.5(SNRNP200):c.4029C>T (p.Asp1343=) rs145242546 0.00017
NM_014014.5(SNRNP200):c.390T>C (p.Asp130=) rs138291954 0.00016
NM_014014.5(SNRNP200):c.5409C>T (p.Ser1803=) rs139137932 0.00016
NM_014014.5(SNRNP200):c.4056G>A (p.Thr1352=) rs758645617 0.00011
NM_014014.5(SNRNP200):c.423T>C (p.Ala141=) rs140702204 0.00011
NM_014014.5(SNRNP200):c.87C>T (p.Asp29=) rs140629902 0.00010
NM_014014.5(SNRNP200):c.6093-6C>T rs202243080 0.00008
NM_014014.5(SNRNP200):c.1485G>A (p.Thr495=) rs142142479 0.00006
NM_014014.5(SNRNP200):c.1098C>T (p.Thr366=) rs774935614 0.00005
NM_014014.5(SNRNP200):c.4721T>C (p.Ile1574Thr) rs199736893 0.00005
NM_014014.5(SNRNP200):c.4966G>A (p.Val1656Met) rs142585893 0.00005
NM_014014.5(SNRNP200):c.2005C>T (p.Pro669Ser) rs749791210 0.00004
NM_014014.5(SNRNP200):c.4728C>T (p.Ile1576=) rs377641548 0.00004
NM_014014.5(SNRNP200):c.651C>T (p.Tyr217=) rs147219591 0.00004
NM_014014.5(SNRNP200):c.*287C>G rs754113881 0.00003
NM_014014.5(SNRNP200):c.2927C>T (p.Thr976Met) rs368406136 0.00003
NM_014014.5(SNRNP200):c.*333G>A rs886056455 0.00002
NM_014014.5(SNRNP200):c.*337G>A rs886056454 0.00002
NM_014014.5(SNRNP200):c.5346G>A (p.Ser1782=) rs756239767 0.00002
NM_014014.5(SNRNP200):c.5665G>A (p.Val1889Ile) rs200367764 0.00002
NM_014014.5(SNRNP200):c.574+12C>T rs761734438 0.00002
NM_014014.5(SNRNP200):c.6174+4C>T rs774620973 0.00002
NM_014014.5(SNRNP200):c.93C>T (p.Thr31=) rs886056468 0.00002
NM_014014.5(SNRNP200):c.*209T>C rs886056456 0.00001
NM_014014.5(SNRNP200):c.1148G>A (p.Arg383His) rs536493402 0.00001
NM_014014.5(SNRNP200):c.1996C>T (p.Arg666Cys) rs200546584 0.00001
NM_014014.5(SNRNP200):c.2268A>G (p.Ser756=) rs370694903 0.00001
NM_014014.5(SNRNP200):c.2542G>A (p.Asp848Asn) rs757811344 0.00001
NM_014014.5(SNRNP200):c.3744C>T (p.Asp1248=) rs750593383 0.00001
NM_014014.5(SNRNP200):c.5336G>A (p.Arg1779His) rs749546665 0.00001
NM_014014.5(SNRNP200):c.6025C>T (p.Arg2009Cys) rs745836206 0.00001
NM_014014.5(SNRNP200):c.6092+3G>A rs751502439 0.00001
NM_014014.5(SNRNP200):c.6291A>G (p.Pro2097=) rs886056457 0.00001
NM_014014.5(SNRNP200):c.781C>A (p.Arg261=) rs746654808 0.00001
NM_014014.5(SNRNP200):c.1498C>T (p.Leu500=) rs886056464
NM_014014.5(SNRNP200):c.1515+11C>A rs780821025
NM_014014.5(SNRNP200):c.162C>T (p.Asp54=) rs2063976140
NM_014014.5(SNRNP200):c.2222T>C (p.Met741Thr) rs886056463
NM_014014.5(SNRNP200):c.2839C>G (p.Pro947Ala) rs886056462
NM_014014.5(SNRNP200):c.3258+12G>A rs886056461
NM_014014.5(SNRNP200):c.3632A>G (p.Asp1211Gly) rs886056460
NM_014014.5(SNRNP200):c.3888C>A (p.Pro1296=) rs143175658
NM_014014.5(SNRNP200):c.4424G>A (p.Arg1475His) rs886056459
NM_014014.5(SNRNP200):c.4786G>A (p.Asp1596Asn) rs762326859
NM_014014.5(SNRNP200):c.6037C>T (p.Arg2013Cys) rs935757494
NM_014014.5(SNRNP200):c.6203T>A (p.Ile2068Asn) rs886056458
NM_014014.5(SNRNP200):c.631-4A>T rs886056467
NM_014014.5(SNRNP200):c.808C>A (p.Arg270=) rs886056466
NM_014014.5(SNRNP200):c.972C>T (p.His324=) rs886056465

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