ClinVar Miner

List of variants in gene SNRNP200 reported as benign

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Gene type:
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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_014014.5(SNRNP200):c.5755-20A>G rs3214063 0.31866
NM_014014.5(SNRNP200):c.3550T>C (p.Leu1184=) rs3171927 0.22368
NM_014014.5(SNRNP200):c.5386C>T (p.Leu1796=) rs34435094 0.02646
NM_014014.5(SNRNP200):c.2422-8C>T rs79583389 0.02643
NM_014014.5(SNRNP200):c.5775C>G (p.Ala1925=) rs72825880 0.01765
NM_014014.5(SNRNP200):c.210-11A>T rs113877776 0.00739
NM_014014.5(SNRNP200):c.5933G>C (p.Gly1978Ala) rs75956769 0.00593
NM_014014.5(SNRNP200):c.3876G>A (p.Pro1292=) rs115923152 0.00475
NM_014014.5(SNRNP200):c.1159A>G (p.Met387Val) rs142729495 0.00369
NM_014014.5(SNRNP200):c.3654C>T (p.Ser1218=) rs3214060 0.00353
NM_014014.5(SNRNP200):c.4165G>A (p.Val1389Ile) rs143898031 0.00328
NM_014014.5(SNRNP200):c.5664C>T (p.His1888=) rs139731897 0.00289
NM_014014.5(SNRNP200):c.5418C>T (p.Asp1806=) rs72937669 0.00267
NM_014014.5(SNRNP200):c.4584+18C>T rs371650935 0.00205
NM_014014.5(SNRNP200):c.3315A>G (p.Ala1105=) rs151063400 0.00165
NM_014014.5(SNRNP200):c.5766C>T (p.Leu1922=) rs147427344 0.00133
NM_014014.5(SNRNP200):c.2310+19G>A rs186052281 0.00117
NM_014014.5(SNRNP200):c.4003+17C>G rs374466738 0.00109
NM_014014.5(SNRNP200):c.3005A>G (p.Asn1002Ser) rs143529458 0.00093
NM_014014.5(SNRNP200):c.273G>A (p.Ser91=) rs115907254 0.00073
NM_014014.5(SNRNP200):c.1854T>C (p.His618=) rs147622706 0.00056
NM_014014.5(SNRNP200):c.4165-6C>T rs372471318 0.00054
NM_014014.5(SNRNP200):c.4935G>A (p.Val1645=) rs375650263 0.00051
NM_014014.5(SNRNP200):c.6369C>T (p.Ser2123=) rs61753580 0.00047
NM_014014.5(SNRNP200):c.2800A>G (p.Thr934Ala) rs149616320 0.00042
NM_014014.5(SNRNP200):c.3640-15T>C rs200824314 0.00036
NM_014014.5(SNRNP200):c.1794C>A (p.Arg598=) rs145902532 0.00030
NM_014014.5(SNRNP200):c.5488+19C>T rs370095598 0.00028
NM_014014.5(SNRNP200):c.3924C>T (p.Pro1308=) rs765746512 0.00020
NM_014014.5(SNRNP200):c.1203+9C>T rs753985092 0.00016
NM_014014.5(SNRNP200):c.5409C>T (p.Ser1803=) rs139137932 0.00016
NM_014014.5(SNRNP200):c.5538C>T (p.Ile1846=) rs201513678 0.00015
NM_014014.5(SNRNP200):c.4393-10C>T rs372636600 0.00014
NM_014014.5(SNRNP200):c.423T>C (p.Ala141=) rs140702204 0.00011
NM_014014.5(SNRNP200):c.90G>C (p.Arg30=) rs374762800 0.00009
NM_014014.5(SNRNP200):c.2857C>A (p.Arg953=) rs150917167 0.00007
NM_014014.5(SNRNP200):c.5488+9C>T rs200122357 0.00007
NM_014014.5(SNRNP200):c.983-7T>C rs778082108 0.00006
NM_014014.5(SNRNP200):c.4377C>T (p.Ile1459=) rs191438128 0.00004
NM_014014.5(SNRNP200):c.5346G>A (p.Ser1782=) rs756239767 0.00002
NM_014014.5(SNRNP200):c.5943T>C (p.Ser1981=) rs754294342 0.00002
NM_014014.5(SNRNP200):c.6093-7C>A rs201143866 0.00002
NM_014014.5(SNRNP200):c.*257C>G rs560814451 0.00001
NM_014014.5(SNRNP200):c.1662C>T (p.Ser554=) rs572113985 0.00001
NM_014014.5(SNRNP200):c.2457G>A (p.Val819=) rs778673233 0.00001
NM_014014.5(SNRNP200):c.2742+8dup rs758931100 0.00001
NM_014014.5(SNRNP200):c.4080A>T (p.Ala1360=) rs547112938 0.00001
NM_014014.5(SNRNP200):c.4205A>G (p.Asn1402Ser) rs560485569 0.00001
NM_014014.5(SNRNP200):c.4818C>T (p.Asp1606=) rs573289061 0.00001
NM_014014.5(SNRNP200):c.5520C>G (p.Thr1840=) rs368225080 0.00001
NM_014014.5(SNRNP200):c.1338T>C (p.His446=)
NM_014014.5(SNRNP200):c.1671+18T>C rs55658279
NM_014014.5(SNRNP200):c.3897C>G (p.Thr1299=) rs144934076
NM_014014.5(SNRNP200):c.574+10C>T rs368132966
NM_014014.5(SNRNP200):c.5983G>A (p.Ala1995Thr) rs201691299
NM_014014.5(SNRNP200):c.723G>A (p.Ser241=) rs2276647
NM_014014.5(SNRNP200):c.732C>T (p.Leu244=) rs199688602

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