ClinVar Miner

List of variants in gene RRP9 studied for not specified

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_004704.5(RRP9):c.1052G>T (p.Gly351Val) rs200319255 0.00025
NM_004704.5(RRP9):c.29G>T (p.Arg10Leu) rs111654088 0.00021
NM_004704.5(RRP9):c.31G>C (p.Gly11Arg) rs1170172847 0.00014
NM_004704.5(RRP9):c.421G>A (p.Val141Ile) rs376449777 0.00009
NM_004704.5(RRP9):c.355C>G (p.Gln119Glu) rs140696554 0.00007
NM_004704.5(RRP9):c.44C>T (p.Ser15Phe) rs748763265 0.00005
NM_004704.5(RRP9):c.419G>A (p.Arg140His) rs113804016 0.00004
NM_004704.5(RRP9):c.19G>C (p.Ala7Pro) rs556392866 0.00003
NM_004704.5(RRP9):c.841G>A (p.Gly281Arg) rs1288640186 0.00002
NM_004704.5(RRP9):c.1411C>A (p.Pro471Thr) rs1324619155 0.00001
NM_004704.5(RRP9):c.144G>C (p.Glu48Asp) rs772740789 0.00001
NM_004704.5(RRP9):c.893T>C (p.Val298Ala) rs200913668 0.00001
NM_004704.5(RRP9):c.962A>G (p.Tyr321Cys) rs749121006 0.00001
NM_004704.5(RRP9):c.1085G>A (p.Arg362His)
NM_004704.5(RRP9):c.1103G>A (p.Arg368Gln) rs557872868
NM_004704.5(RRP9):c.1103G>T (p.Arg368Leu) rs557872868
NM_004704.5(RRP9):c.1105G>A (p.Gly369Arg)
NM_004704.5(RRP9):c.1255C>G (p.Pro419Ala)
NM_004704.5(RRP9):c.1292G>T (p.Ser431Ile)
NM_004704.5(RRP9):c.14C>G (p.Ala5Gly) rs1225981129
NM_004704.5(RRP9):c.197A>C (p.Glu66Ala)
NM_004704.5(RRP9):c.212T>C (p.Leu71Pro)
NM_004704.5(RRP9):c.23G>A (p.Arg8His) rs373215221
NM_004704.5(RRP9):c.272G>T (p.Arg91Leu) rs374405922
NM_004704.5(RRP9):c.293C>G (p.Ala98Gly) rs777793041
NM_004704.5(RRP9):c.35A>G (p.Lys12Arg)
NM_004704.5(RRP9):c.445A>G (p.Ile149Val) rs1449462352
NM_004704.5(RRP9):c.44C>G (p.Ser15Cys)
NM_004704.5(RRP9):c.535C>T (p.Arg179Trp)
NM_004704.5(RRP9):c.566A>G (p.Lys189Arg)
NM_004704.5(RRP9):c.623C>G (p.Ser208Cys) rs768365555
NM_004704.5(RRP9):c.62C>A (p.Ala21Glu)
NM_004704.5(RRP9):c.722G>T (p.Arg241Leu) rs376861276
NM_004704.5(RRP9):c.784G>A (p.Asp262Asn)
NM_004704.5(RRP9):c.797A>G (p.Lys266Arg) rs967504043
NM_004704.5(RRP9):c.908G>A (p.Arg303Gln)
NM_004704.5(RRP9):c.992A>G (p.His331Arg) rs1699442388

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