ClinVar Miner

List of variants in gene CSRP3 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 80
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HGVS dbSNP gnomAD frequency
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.49G>A (p.Val17Ile) rs767932680 0.00009
NM_003476.5(CSRP3):c.131T>C (p.Leu44Pro) rs104894205 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.230C>G (p.Ala77Gly) rs772138289 0.00004
NM_003476.5(CSRP3):c.298C>T (p.Arg100Cys) rs201214593 0.00004
NM_003476.5(CSRP3):c.365G>A (p.Arg122Gln) rs193922667 0.00004
NM_003476.5(CSRP3):c.436C>T (p.Arg146Cys) rs376198883 0.00004
NM_003476.5(CSRP3):c.536C>T (p.Thr179Met) rs142019584 0.00004
NM_003476.5(CSRP3):c.-3A>C rs760384315 0.00003
NM_003476.5(CSRP3):c.140C>T (p.Thr47Met) rs397516851 0.00003
NM_003476.5(CSRP3):c.214G>A (p.Gly72Arg) rs45552933 0.00003
NM_003476.5(CSRP3):c.256G>A (p.Glu86Lys) rs780917755 0.00003
NM_003476.5(CSRP3):c.287C>T (p.Pro96Leu) rs766783066 0.00003
NM_003476.5(CSRP3):c.352G>A (p.Glu118Lys) rs763096875 0.00003
NM_003476.5(CSRP3):c.568G>T (p.Val190Leu) rs145073736 0.00003
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.255C>T (p.Gly85=) rs752338221 0.00001
NM_003476.5(CSRP3):c.283T>G (p.Ser95Ala) rs1190724900 0.00001
NM_003476.5(CSRP3):c.284C>T (p.Ser95Phe) rs767477787 0.00001
NM_003476.5(CSRP3):c.29G>A (p.Cys10Tyr) rs141980088 0.00001
NM_003476.5(CSRP3):c.302C>T (p.Ser101Leu) rs746707959 0.00001
NM_003476.5(CSRP3):c.367T>C (p.Cys123Arg) rs1301857786 0.00001
NM_003476.5(CSRP3):c.369T>A (p.Cys123Ter) rs1216811263 0.00001
NM_003476.5(CSRP3):c.40G>C (p.Glu14Gln) rs777883490 0.00001
NM_003476.5(CSRP3):c.415-1G>T rs775194825 0.00001
NM_003476.5(CSRP3):c.576G>C (p.Lys192Asn) rs141100524 0.00001
NM_003476.5(CSRP3):c.86G>A (p.Ser29Asn) rs372717179 0.00001
NM_003476.5(CSRP3):c.10_11del (p.Trp4fs) rs1554968150
NM_003476.5(CSRP3):c.116C>A (p.Ala39Asp) rs748417030
NM_003476.5(CSRP3):c.136A>T (p.Ser46Cys)
NM_003476.5(CSRP3):c.149C>T (p.Ala50Val) rs139805841
NM_003476.5(CSRP3):c.161C>T (p.Ser54Leu)
NM_003476.5(CSRP3):c.163G>A (p.Glu55Lys)
NM_003476.5(CSRP3):c.172T>G (p.Cys58Gly) rs104894204
NM_003476.5(CSRP3):c.190C>A (p.Arg64Ser)
NM_003476.5(CSRP3):c.200G>A (p.Gly67Asp)
NM_003476.5(CSRP3):c.208G>T (p.Gly70Trp) rs777211110
NM_003476.5(CSRP3):c.209G>T (p.Gly70Val)
NM_003476.5(CSRP3):c.229G>T (p.Ala77Ser) rs746207
NM_003476.5(CSRP3):c.233G>T (p.Gly78Val) rs963128995
NM_003476.5(CSRP3):c.236G>C (p.Cys79Ser)
NM_003476.5(CSRP3):c.251C>G (p.Thr84Arg)
NM_003476.5(CSRP3):c.259C>T (p.His87Tyr)
NM_003476.5(CSRP3):c.265G>A (p.Gly89Ser) rs367827746
NM_003476.5(CSRP3):c.286_287del (p.Pro96fs) rs960577385
NM_003476.5(CSRP3):c.311C>A (p.Thr104Asn)
NM_003476.5(CSRP3):c.329del (p.Phe110fs) rs2133508524
NM_003476.5(CSRP3):c.334G>C (p.Ala112Pro) rs727504905
NM_003476.5(CSRP3):c.335C>A (p.Ala112Glu)
NM_003476.5(CSRP3):c.377C>A (p.Ser126Ter)
NM_003476.5(CSRP3):c.37T>C (p.Cys13Arg) rs1257113692
NM_003476.5(CSRP3):c.3G>A (p.Met1Ile)
NM_003476.5(CSRP3):c.403G>A (p.Gly135Arg) rs1850522271
NM_003476.5(CSRP3):c.415-2A>C rs1850502742
NM_003476.5(CSRP3):c.424A>G (p.Lys142Glu) rs2133506962
NM_003476.5(CSRP3):c.439T>C (p.Cys147Arg) rs2133506925
NM_003476.5(CSRP3):c.455A>G (p.Lys152Arg)
NM_003476.5(CSRP3):c.457_458del (p.Leu154fs) rs748393033
NM_003476.5(CSRP3):c.458G>T (p.Ser153Ile)
NM_003476.5(CSRP3):c.496C>G (p.Leu166Val)
NM_003476.5(CSRP3):c.4C>T (p.Pro2Ser)
NM_003476.5(CSRP3):c.511T>C (p.Cys171Arg)
NM_003476.5(CSRP3):c.532C>G (p.Pro178Ala) rs749002955
NM_003476.5(CSRP3):c.539G>T (p.Gly180Val) rs727504899
NM_003476.5(CSRP3):c.541A>G (p.Ile181Val)
NM_003476.5(CSRP3):c.572A>T (p.Glu191Val)
NM_003476.5(CSRP3):c.575del (p.Lys192fs) rs1554967246
NM_003476.5(CSRP3):c.580G>C (p.Glu194Gln)
NM_003476.5(CSRP3):c.583T>A (p.Ter195Arg) rs774359383
NM_003476.5(CSRP3):c.64G>T (p.Glu22Ter)
NM_003476.5(CSRP3):c.72G>C (p.Gln24His)
NM_003476.5(CSRP3):c.88T>C (p.Phe30Leu) rs2133516315

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