ClinVar Miner

List of variants in gene FKRP reported as likely benign for not provided

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Gene type:
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Total variants: 24
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HGVS dbSNP
NM_024301.5(FKRP):c.-206G>T rs1263835324
NM_024301.5(FKRP):c.-39-243A>G rs184686014
NM_024301.5(FKRP):c.1041G>A (p.Leu347=) rs1599938600
NM_024301.5(FKRP):c.1167G>A (p.Glu389=) rs771708277
NM_024301.5(FKRP):c.1233C>T (p.Asn411=) rs1451916862
NM_024301.5(FKRP):c.1368C>T (p.Gly456=) rs1599940206
NM_024301.5(FKRP):c.1386T>G (p.Pro462=) rs776825755
NM_024301.5(FKRP):c.18C>T (p.Cys6=) rs373388363
NM_024301.5(FKRP):c.235G>A (p.Val79Met) rs104894683
NM_024301.5(FKRP):c.321C>T (p.Ala107=) rs1599934722
NM_024301.5(FKRP):c.336C>T (p.Ala112=) rs1054339656
NM_024301.5(FKRP):c.345G>A (p.Ser115=) rs1356142931
NM_024301.5(FKRP):c.351G>A (p.Pro117=) rs1060504470
NM_024301.5(FKRP):c.360C>T (p.Tyr120=) rs781576638
NM_024301.5(FKRP):c.375T>C (p.Phe125=) rs1599934927
NM_024301.5(FKRP):c.427C>A (p.Arg143Ser) rs148206382
NM_024301.5(FKRP):c.474C>G (p.Ala158=) rs963599756
NM_024301.5(FKRP):c.522C>T (p.Ser174=) rs1599935593
NM_024301.5(FKRP):c.526C>A (p.Arg176=) rs1555738502
NM_024301.5(FKRP):c.561C>G (p.Ala187=) rs771770302
NM_024301.5(FKRP):c.576C>T (p.Asp192=) rs1366277135
NM_024301.5(FKRP):c.678C>G (p.Thr226=) rs1060504471
NM_024301.5(FKRP):c.822C>G (p.Ile274Met) rs77138370
NM_024301.5(FKRP):c.885C>T (p.Arg295=) rs769005880

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