ClinVar Miner

List of variants in gene GPRC5D reported as uncertain significance for not specified

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_018654.2(GPRC5D):c.581G>A (p.Gly194Asp) rs151110753 0.00025
NM_018654.2(GPRC5D):c.819C>G (p.Cys273Trp) rs146288496 0.00022
NM_018654.2(GPRC5D):c.684C>A (p.Asn228Lys) rs201518268 0.00021
NM_018654.2(GPRC5D):c.665C>T (p.Ser222Phe) rs145033785 0.00009
NM_018654.2(GPRC5D):c.487C>T (p.Pro163Ser) rs922088890 0.00008
NM_018654.2(GPRC5D):c.679G>A (p.Gly227Ser) rs377356062 0.00007
NM_018654.2(GPRC5D):c.271G>A (p.Val91Ile) rs138250506 0.00003
NM_018654.2(GPRC5D):c.275G>A (p.Arg92His) rs1050579210 0.00002
NM_018654.2(GPRC5D):c.185C>T (p.Thr62Ile) rs1299860267 0.00001
NM_018654.2(GPRC5D):c.395T>C (p.Ile132Thr) rs778141045 0.00001
NM_018654.2(GPRC5D):c.559G>A (p.Val187Ile) rs151293943 0.00001
NM_018654.2(GPRC5D):c.578G>A (p.Cys193Tyr) rs750194630 0.00001
NM_018654.2(GPRC5D):c.605A>G (p.His202Arg) rs1453684663 0.00001
NM_018654.2(GPRC5D):c.719C>T (p.Pro240Leu) rs373330973 0.00001
NM_018654.2(GPRC5D):c.880C>G (p.Gln294Glu) rs757664681 0.00001
NM_018654.2(GPRC5D):c.103G>A (p.Val35Met)
NM_018654.2(GPRC5D):c.146G>A (p.Arg49Gln)
NM_018654.2(GPRC5D):c.229G>A (p.Ala77Thr) rs138218691
NM_018654.2(GPRC5D):c.280T>C (p.Phe94Leu)
NM_018654.2(GPRC5D):c.305T>G (p.Leu102Arg)
NM_018654.2(GPRC5D):c.337A>C (p.Asn113His)
NM_018654.2(GPRC5D):c.338A>G (p.Asn113Ser)
NM_018654.2(GPRC5D):c.348G>T (p.Lys116Asn)
NM_018654.2(GPRC5D):c.438G>T (p.Glu146Asp) rs2497678036
NM_018654.2(GPRC5D):c.468G>A (p.Met156Ile) rs1379648758
NM_018654.2(GPRC5D):c.500A>G (p.Asn167Ser) rs138805879
NM_018654.2(GPRC5D):c.55G>A (p.Glu19Lys) rs377647570
NM_018654.2(GPRC5D):c.708G>T (p.Gln236His) rs764873589
NM_018654.2(GPRC5D):c.751T>C (p.Trp251Arg)
NM_018654.2(GPRC5D):c.899G>A (p.Arg300Gln)
NM_018654.2(GPRC5D):c.944G>A (p.Gly315Asp)
NM_018654.2(GPRC5D):c.949C>T (p.Pro317Ser)
NM_018654.2(GPRC5D):c.961C>G (p.Gln321Glu)

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