ClinVar Miner

List of variants in gene CSRP3 reported as likely benign for cardiomyopathy

Included ClinVar conditions (522):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_003476.5(CSRP3):c.312C>G (p.Thr104=) rs45582433 0.01721
NM_003476.4(CSRP3):c.-252G>A rs59444364 0.01356
NM_003476.5(CSRP3):c.213C>T (p.Ile71=) rs45476991 0.00499
NM_003476.5(CSRP3):c.*450T>G rs45479995 0.00318
NM_003476.5(CSRP3):c.10T>C (p.Trp4Arg) rs45550635 0.00271
NM_003476.5(CSRP3):c.*12G>A rs45607943 0.00108
NM_003476.5(CSRP3):c.162G>A (p.Ser54=) rs112848043 0.00104
NM_003476.5(CSRP3):c.299G>A (p.Arg100His) rs138218523 0.00097
NM_003476.5(CSRP3):c.16G>A (p.Gly6Arg) rs185980145 0.00006
NM_003476.5(CSRP3):c.294G>A (p.Pro98=) rs142832902 0.00006
NM_003476.5(CSRP3):c.415-9G>C rs761203242 0.00006
NM_003476.5(CSRP3):c.258G>A (p.Glu86=) rs182798086 0.00005
NM_003476.5(CSRP3):c.300C>T (p.Arg100=) rs146290726 0.00004
NM_003476.5(CSRP3):c.21C>T (p.Gly7=) rs151177504 0.00003
NM_003476.5(CSRP3):c.282-16C>A rs757074408 0.00003
NM_003476.5(CSRP3):c.99G>A (p.Thr33=) rs147549410 0.00003
NM_003476.5(CSRP3):c.252G>A (p.Thr84=) rs755614464 0.00002
NM_003476.5(CSRP3):c.282-16C>T rs757074408 0.00002
NM_003476.5(CSRP3):c.141G>A (p.Thr47=) rs758842207 0.00001
NM_003476.5(CSRP3):c.15C>T (p.Gly5=) rs747959696 0.00001
NM_003476.5(CSRP3):c.201C>T (p.Gly67=) rs557643642 0.00001
NM_003476.5(CSRP3):c.210G>A (p.Gly70=) rs1330897950 0.00001
NM_003476.5(CSRP3):c.228C>T (p.Gly76=) rs768767452 0.00001
NM_003476.5(CSRP3):c.261T>C (p.His87=) rs773476497 0.00001
NM_003476.5(CSRP3):c.264C>A (p.Leu88=) rs758256351 0.00001
NM_003476.5(CSRP3):c.279A>G (p.Gln93=) rs1394545167 0.00001
NM_003476.5(CSRP3):c.309C>G (p.Thr103=) rs1273565241 0.00001
NM_003476.5(CSRP3):c.339G>A (p.Lys113=) rs1394465819 0.00001
NM_003476.5(CSRP3):c.351C>T (p.Ser117=) rs766621810 0.00001
NM_003476.5(CSRP3):c.414+16T>C rs778831593 0.00001
NM_003476.5(CSRP3):c.465G>A (p.Glu155=) rs200334242 0.00001
NM_003476.5(CSRP3):c.48C>T (p.Thr16=) rs753120437 0.00001
NM_003476.5(CSRP3):c.501T>C (p.Tyr167=) rs1161551238 0.00001
NM_003476.5(CSRP3):c.509-16C>T rs371700321 0.00001
NM_003476.5(CSRP3):c.513C>T (p.Cys171=) rs376799144 0.00001
NM_003476.5(CSRP3):c.516T>C (p.Tyr172=) rs727504575 0.00001
NM_003476.5(CSRP3):c.538G>T (p.Gly180Cys) rs547374738 0.00001
NM_003476.5(CSRP3):c.90C>T (p.Phe30=) rs772727223 0.00001
NM_003476.5(CSRP3):c.108C>T (p.His36=) rs763193066
NM_003476.5(CSRP3):c.112+11T>C
NM_003476.5(CSRP3):c.112+12G>A
NM_003476.5(CSRP3):c.112+19C>T
NM_003476.5(CSRP3):c.112+9G>A rs2133516226
NM_003476.5(CSRP3):c.113-17C>A
NM_003476.5(CSRP3):c.113-17C>T
NM_003476.5(CSRP3):c.113-20A>T
NM_003476.5(CSRP3):c.120C>T (p.Cys40=)
NM_003476.5(CSRP3):c.123G>A (p.Arg41=) rs1590104476
NM_003476.5(CSRP3):c.126G>A (p.Lys42=)
NM_003476.5(CSRP3):c.141G>T (p.Thr47=)
NM_003476.5(CSRP3):c.144A>C (p.Thr48=)
NM_003476.5(CSRP3):c.147C>T (p.Val49=) rs576346189
NM_003476.5(CSRP3):c.156T>C (p.His52=)
NM_003476.5(CSRP3):c.15C>A (p.Gly5=) rs747959696
NM_003476.5(CSRP3):c.162G>T (p.Ser54=)
NM_003476.5(CSRP3):c.198T>C (p.Tyr66=) rs779421059
NM_003476.5(CSRP3):c.201C>A (p.Gly67=) rs557643642
NM_003476.5(CSRP3):c.216G>T (p.Gly72=) rs751348376
NM_003476.5(CSRP3):c.222A>C (p.Gly74=)
NM_003476.5(CSRP3):c.231T>C (p.Ala77=)
NM_003476.5(CSRP3):c.240C>G (p.Leu80=)
NM_003476.5(CSRP3):c.240C>T (p.Leu80=)
NM_003476.5(CSRP3):c.255C>A (p.Gly85=) rs752338221
NM_003476.5(CSRP3):c.264C>T (p.Leu88=) rs758256351
NM_003476.5(CSRP3):c.270G>C (p.Leu90=)
NM_003476.5(CSRP3):c.273G>A (p.Gln91=)
NM_003476.5(CSRP3):c.282-15G>A
NM_003476.5(CSRP3):c.282-19A>G
NM_003476.5(CSRP3):c.285C>A (p.Ser95=) rs45483799
NM_003476.5(CSRP3):c.285C>T (p.Ser95=)
NM_003476.5(CSRP3):c.294G>C (p.Pro98=) rs142832902
NM_003476.5(CSRP3):c.324C>T (p.Ser108=)
NM_003476.5(CSRP3):c.345A>G (p.Gly115=)
NM_003476.5(CSRP3):c.348G>A (p.Glu116=) rs2133508450
NM_003476.5(CSRP3):c.36C>T (p.Ala12=) rs2133516477
NM_003476.5(CSRP3):c.381C>A (p.Val127=) rs2133508364
NM_003476.5(CSRP3):c.411C>A (p.Gly137=) rs1411552973
NM_003476.5(CSRP3):c.414+7C>A
NM_003476.5(CSRP3):c.414+7C>T
NM_003476.5(CSRP3):c.414+8C>T
NM_003476.5(CSRP3):c.415-11G>A
NM_003476.5(CSRP3):c.415-11G>T rs886048097
NM_003476.5(CSRP3):c.415-16T>C rs2133507025
NM_003476.5(CSRP3):c.415-18C>G
NM_003476.5(CSRP3):c.415-6C>T
NM_003476.5(CSRP3):c.480T>C (p.Thr160=) rs2133506829
NM_003476.5(CSRP3):c.508+17A>G rs373822409
NM_003476.5(CSRP3):c.508+17A>T rs373822409
NM_003476.5(CSRP3):c.508+7G>T
NM_003476.5(CSRP3):c.508+9_508+15dup
NM_003476.5(CSRP3):c.509-20C>T
NM_003476.5(CSRP3):c.509-3_509-2del rs397516858
NM_003476.5(CSRP3):c.509-5C>T rs1447306323
NM_003476.5(CSRP3):c.509-8A>G rs2133503964
NM_003476.5(CSRP3):c.51C>A (p.Val17=)
NM_003476.5(CSRP3):c.76A>G (p.Asn26Asp) rs1408098337

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