ClinVar Miner

List of variants in gene PRR12 reported as likely benign for not provided

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_020719.3(PRR12):c.2315A>T (p.Gln772Leu) rs201499347 0.00235
NM_020719.3(PRR12):c.3373G>A (p.Val1125Ile) rs202038770 0.00197
NM_020719.3(PRR12):c.2702C>G (p.Pro901Arg) rs547414671 0.00107
NM_020719.3(PRR12):c.342C>T (p.Arg114=) rs375190208 0.00106
NM_020719.3(PRR12):c.1606G>A (p.Gly536Ser) rs200340380 0.00103
NM_020719.3(PRR12):c.4466T>C (p.Val1489Ala) rs765584966 0.00051
NM_020719.3(PRR12):c.3240G>A (p.Leu1080=) rs768682542 0.00026
NM_020719.3(PRR12):c.2394C>T (p.Pro798=) rs758817354 0.00018
NM_020719.3(PRR12):c.3963C>T (p.Gly1321=) rs367748904 0.00016
NM_020719.3(PRR12):c.657C>T (p.Leu219=) rs373856538 0.00015
NM_020719.3(PRR12):c.2208C>T (p.Gly736=) rs557659919 0.00004
NM_020719.3(PRR12):c.2790C>T (p.Thr930=) rs1173175968 0.00004
NM_020719.3(PRR12):c.2847C>A (p.Thr949=) rs1187816188 0.00004
NM_020719.3(PRR12):c.615C>T (p.Phe205=) rs559236267 0.00004
NM_020719.3(PRR12):c.2109C>T (p.Val703=) rs765988941 0.00003
NM_020719.3(PRR12):c.4353G>A (p.Pro1451=) rs754327328 0.00003
NM_020719.3(PRR12):c.4200C>T (p.Ser1400=) rs772116961 0.00002
NM_020719.3(PRR12):c.2838C>T (p.Phe946=) rs761439398 0.00001
NM_020719.3(PRR12):c.5139G>A (p.Lys1713=) rs753024807 0.00001
NM_020719.3(PRR12):c.1110C>G (p.Gly370=)
NM_020719.3(PRR12):c.1118C>T (p.Ala373Val)
NM_020719.3(PRR12):c.1128T>G (p.Gly376=)
NM_020719.3(PRR12):c.1388G>C (p.Gly463Ala)
NM_020719.3(PRR12):c.183C>T (p.Thr61=)
NM_020719.3(PRR12):c.2025G>T (p.Gly675=)
NM_020719.3(PRR12):c.2041G>A (p.Gly681Arg)
NM_020719.3(PRR12):c.2147C>G (p.Ala716Gly) rs199785002
NM_020719.3(PRR12):c.2151A>C (p.Ala717=)
NM_020719.3(PRR12):c.2201G>A (p.Arg734Gln)
NM_020719.3(PRR12):c.220A>C (p.Thr74Pro)
NM_020719.3(PRR12):c.2508T>C (p.Pro836=)
NM_020719.3(PRR12):c.2514G>C (p.Pro838=)
NM_020719.3(PRR12):c.2517A>C (p.Pro839=)
NM_020719.3(PRR12):c.2586G>A (p.Ala862=)
NM_020719.3(PRR12):c.2600G>A (p.Arg867His)
NM_020719.3(PRR12):c.261C>T (p.Ser87=)
NM_020719.3(PRR12):c.2992G>T (p.Ala998Ser)
NM_020719.3(PRR12):c.3300G>A (p.Glu1100=)
NM_020719.3(PRR12):c.3991G>A (p.Ala1331Thr)
NM_020719.3(PRR12):c.4280C>T (p.Ala1427Val)
NM_020719.3(PRR12):c.4455A>C (p.Pro1485=)
NM_020719.3(PRR12):c.4475C>T (p.Thr1492Met)
NM_020719.3(PRR12):c.4488_4499del (p.Pro1497_Pro1500del)
NM_020719.3(PRR12):c.4505C>T (p.Pro1502Leu)
NM_020719.3(PRR12):c.4686C>T (p.Asp1562=)
NM_020719.3(PRR12):c.5166C>T (p.Ala1722=) rs1599799699
NM_020719.3(PRR12):c.5206C>G (p.Arg1736Gly) rs200319638
NM_020719.3(PRR12):c.5207G>A (p.Arg1736Gln)
NM_020719.3(PRR12):c.5314G>T (p.Ala1772Ser)
NM_020719.3(PRR12):c.5318C>T (p.Thr1773Met)
NM_020719.3(PRR12):c.5700G>A (p.Leu1900=) rs1220719420
NM_020719.3(PRR12):c.5712A>G (p.Pro1904=)
NM_020719.3(PRR12):c.5724T>C (p.Asp1908=)
NM_020719.3(PRR12):c.633C>T (p.Gly211=)
NM_020719.3(PRR12):c.807G>A (p.Ser269=)
NM_020719.3(PRR12):c.903A>C (p.Pro301=)

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