ClinVar Miner

List of variants in gene CSRP3 reported by Fulgent Genetics, Fulgent Genetics

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_003476.5(CSRP3):c.312C>G (p.Thr104=) rs45582433 0.01721
NM_003476.5(CSRP3):c.*12G>A rs45607943 0.00108
NM_003476.5(CSRP3):c.*245T>C rs369635973 0.00081
NM_003476.5(CSRP3):c.*638T>C rs779532194 0.00056
NM_003476.5(CSRP3):c.*415A>G rs180844111 0.00032
NM_003476.5(CSRP3):c.175A>G (p.Lys59Glu) rs769003538 0.00016
NM_003476.5(CSRP3):c.544G>C (p.Gly182Arg) rs111868331 0.00011
NM_003476.5(CSRP3):c.190C>T (p.Arg64Cys) rs368392588 0.00009
NM_003476.5(CSRP3):c.272A>T (p.Gln91Leu) rs727504436 0.00009
NM_003476.5(CSRP3):c.379G>A (p.Val127Ile) rs149201422 0.00009
NM_003476.5(CSRP3):c.49G>A (p.Val17Ile) rs767932680 0.00009
NM_003476.5(CSRP3):c.148G>A (p.Ala50Thr) rs145300736 0.00006
NM_003476.5(CSRP3):c.136A>C (p.Ser46Arg) rs137852765 0.00005
NM_003476.5(CSRP3):c.535A>G (p.Thr179Ala) rs397516859 0.00005
NM_003476.5(CSRP3):c.298C>T (p.Arg100Cys) rs201214593 0.00004
NM_003476.5(CSRP3):c.436C>T (p.Arg146Cys) rs376198883 0.00004
NM_003476.5(CSRP3):c.*575T>C rs886048093 0.00003
NM_003476.5(CSRP3):c.140C>T (p.Thr47Met) rs397516851 0.00003
NM_003476.5(CSRP3):c.437G>A (p.Arg146His) rs377066670 0.00002
NM_003476.5(CSRP3):c.152C>A (p.Ala51Asp) rs397516853 0.00001
NM_003476.5(CSRP3):c.168C>G (p.Ile56Met) rs767360228 0.00001
NM_003476.5(CSRP3):c.206A>G (p.Lys69Arg) rs137852764 0.00001
NM_003476.5(CSRP3):c.251C>T (p.Thr84Met) rs777327517 0.00001
NM_003476.5(CSRP3):c.86G>A (p.Ser29Asn) rs372717179 0.00001
NM_003476.5(CSRP3):c.98C>T (p.Thr33Met) rs758947977 0.00001
NM_003476.4(CSRP3):c.-195G>A rs569978006
NM_003476.5(CSRP3):c.*159C>T rs886048095
NM_003476.5(CSRP3):c.*559G>A rs45606836
NM_003476.5(CSRP3):c.149C>A (p.Ala50Glu) rs139805841
NM_003476.5(CSRP3):c.149C>T (p.Ala50Val) rs139805841
NM_003476.5(CSRP3):c.159G>C (p.Glu53Asp) rs1253887422
NM_003476.5(CSRP3):c.208G>T (p.Gly70Trp) rs777211110
NM_003476.5(CSRP3):c.286_287del (p.Pro96fs) rs960577385
NM_003476.5(CSRP3):c.335C>T (p.Ala112Val) rs753711278
NM_003476.5(CSRP3):c.354G>C (p.Glu118Asp) rs876657767

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