ClinVar Miner

List of variants in gene PROKR2 reported by Fulgent Genetics, Fulgent Genetics

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_144773.4(PROKR2):c.1122C>A (p.Thr374=) rs76469093 0.00085
NM_144773.4(PROKR2):c.390C>T (p.Ser130=) rs144778137 0.00054
NM_144773.4(PROKR2):c.376G>A (p.Val126Met) rs200048973 0.00014
NM_144773.4(PROKR2):c.156C>T (p.Ala52=) rs775513724 0.00012
NM_144773.4(PROKR2):c.868C>T (p.Pro290Ser) rs149992595 0.00010
NM_144773.4(PROKR2):c.491G>A (p.Arg164Gln) rs751875578 0.00009
NM_144773.4(PROKR2):c.349C>T (p.Arg117Trp) rs142008002 0.00006
NM_144773.4(PROKR2):c.803G>A (p.Arg268His) rs781065670 0.00004
NM_144773.4(PROKR2):c.742C>T (p.Arg248Trp) rs483352766 0.00003
NM_144773.4(PROKR2):c.537G>A (p.Met179Ile) rs770233566 0.00002
NM_144773.4(PROKR2):c.563C>T (p.Ser188Leu) rs376239580 0.00002
NM_144773.4(PROKR2):c.208G>A (p.Gly70Ser) rs764674615 0.00001
NM_144773.4(PROKR2):c.663G>A (p.Lys221=) rs1051636587 0.00001
NM_144773.4(PROKR2):c.1042A>C (p.Met348Leu) rs368145317
NM_144773.4(PROKR2):c.1050G>A (p.Leu350=) rs779816527
NM_144773.4(PROKR2):c.1111G>A (p.Gly371Arg) rs201023639
NM_144773.4(PROKR2):c.254G>A (p.Arg85His) rs74315418
NM_144773.4(PROKR2):c.525C>A (p.Ala175=) rs3746683

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