ClinVar Miner

List of variants in gene CSRP3 reported as uncertain significance for Cardiomyopathy

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_003476.5(CSRP3):c.10T>C (p.Trp4Arg) rs45550635 0.00271
NM_003476.4(CSRP3):c.-74A>C rs45498797 0.00092
NM_003476.5(CSRP3):c.190C>T (p.Arg64Cys) rs368392588 0.00009
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.191G>A (p.Arg64His) rs375014380 0.00003
NM_003476.5(CSRP3):c.568G>T (p.Val190Leu) rs145073736 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.197A>G (p.Tyr66Cys) rs397516854 0.00001
NM_003476.5(CSRP3):c.293C>T (p.Pro98Leu) rs773411006 0.00001
NM_003476.5(CSRP3):c.302C>T (p.Ser101Leu) rs746707959 0.00001
NM_003476.5(CSRP3):c.449G>A (p.Cys150Tyr) rs761507504 0.00001
NM_003476.5(CSRP3):c.10_11del (p.Trp4fs) rs1554968150
NM_003476.5(CSRP3):c.113-9T>C
NM_003476.5(CSRP3):c.17G>A (p.Gly6Glu) rs1431565691
NM_003476.5(CSRP3):c.382T>C (p.Tyr128His) rs1565050687
NM_003476.5(CSRP3):c.457_458del (p.Leu154fs) rs748393033
NM_003476.5(CSRP3):c.497T>G (p.Leu166Arg) rs1565050249
NM_003476.5(CSRP3):c.509-7T>G rs1565049368
NM_003476.5(CSRP3):c.511T>G (p.Cys171Gly) rs770760020
NM_003476.5(CSRP3):c.526T>G (p.Phe176Val) rs2133503927

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