ClinVar Miner

List of variants in gene MYLK reported as uncertain significance for not provided

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Total variants: 65
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HGVS dbSNP
NC_000003.12:g.123657354_123657356delCAT
NM_053025.3(MYLK):c.1170G>C (p.Gly390=) rs1553822363
NM_053025.3(MYLK):c.1340G>C (p.Trp447Ser) rs886043581
NM_053025.3(MYLK):c.149C>T (p.Ala50Val) rs369576521
NM_053025.3(MYLK):c.1569C>T (p.Cys523=) rs150378280
NM_053025.3(MYLK):c.159dupA (p.Gly54Argfs) rs1553850067
NM_053025.3(MYLK):c.1613G>A (p.Arg538Gln) rs368509953
NM_053025.3(MYLK):c.1640G>A (p.Trp547Ter) rs779212460
NM_053025.3(MYLK):c.1991A>G (p.Gln664Arg) rs200273207
NM_053025.3(MYLK):c.2009A>T (p.His670Leu) rs1057524740
NM_053025.3(MYLK):c.2069C>T (p.Thr690Met)
NM_053025.3(MYLK):c.2120A>G (p.Gln707Arg) rs201615936
NM_053025.3(MYLK):c.2125G>A (p.Val709Met) rs112537316
NM_053025.3(MYLK):c.2132C>T (p.Thr711Met) rs531232445
NM_053025.3(MYLK):c.2149G>A (p.Asp717Asn) rs150936840
NM_053025.3(MYLK):c.2183G>A (p.Arg728His) rs370154845
NM_053025.3(MYLK):c.226G>A (p.Gly76Arg) rs368413008
NM_053025.3(MYLK):c.2326G>A (p.Val776Met) rs372707781
NM_053025.3(MYLK):c.2398G>T (p.Val800Phe) rs758697820
NM_053025.3(MYLK):c.2429T>A (p.Met810Lys) rs1553805024
NM_053025.3(MYLK):c.2462+5G>A rs374003770
NM_053025.3(MYLK):c.2474C>T (p.Pro825Leu) rs201332554
NM_053025.3(MYLK):c.2481C>G (p.Ser827Arg) rs1131691270
NM_053025.3(MYLK):c.256C>T (p.Arg86Trp) rs368822172
NM_053025.3(MYLK):c.257G>A (p.Arg86Gln) rs138265409
NM_053025.3(MYLK):c.2584G>C (p.Glu862Gln) rs770667051
NM_053025.3(MYLK):c.2598C>T (p.Gly866=) rs144654396
NM_053025.3(MYLK):c.2629G>A (p.Val877Met) rs34542174
NM_053025.3(MYLK):c.2643G>A (p.Gln881=) rs765727285
NM_053025.3(MYLK):c.2663G>A (p.Arg888His) rs528507616
NM_053025.3(MYLK):c.2740G>T (p.Asp914Tyr)
NM_053025.3(MYLK):c.2791_2792delCGinsAT (p.Arg931Met) rs1553803967
NM_053025.3(MYLK):c.2921C>G (p.Pro974Arg) rs1553803753
NM_053025.3(MYLK):c.3184G>T (p.Ala1062Ser) rs11558550
NM_053025.3(MYLK):c.3193G>C (p.Glu1065Gln) rs1064797009
NM_053025.3(MYLK):c.3380_3382delCCAinsGCC (p.Ala1127_Thr1128delinsGlyPro) rs886043880
NM_053025.3(MYLK):c.344G>A (p.Arg115His) rs141131535
NM_053025.3(MYLK):c.3615G>T (p.Arg1205Ser)
NM_053025.3(MYLK):c.3637G>A (p.Val1213Met) rs368390254
NM_053025.3(MYLK):c.374-3C>A rs1473632768
NM_053025.3(MYLK):c.3824G>A (p.Arg1275Gln) rs564792567
NM_053025.3(MYLK):c.4110C>G (p.Ile1370Met) rs199971683
NM_053025.3(MYLK):c.4336G>A (p.Glu1446Lys) rs146682969
NM_053025.3(MYLK):c.4343A>T (p.Asp1448Val) rs757392371
NM_053025.3(MYLK):c.4425T>G (p.Phe1475Leu) rs1064797297
NM_053025.3(MYLK):c.4538T>C (p.Met1513Thr)
NM_053025.3(MYLK):c.4565T>C (p.Val1522Ala) rs763880352
NM_053025.3(MYLK):c.4681G>C (p.Glu1561Gln) rs1114167363
NM_053025.3(MYLK):c.474G>T (p.Glu158Asp) rs370158852
NM_053025.3(MYLK):c.4915G>A (p.Gly1639Ser) rs143900788
NM_053025.3(MYLK):c.5155C>T (p.Leu1719=) rs1057523680
NM_053025.3(MYLK):c.5253T>C (p.Ala1751=) rs1475852496
NM_053025.3(MYLK):c.5369-10T>G rs373584324
NM_053025.3(MYLK):c.5392G>A (p.Glu1798Lys) rs777616795
NM_053025.3(MYLK):c.5477C>T (p.Ala1826Val) rs147187907
NM_053025.3(MYLK):c.5489G>A (p.Cys1830Tyr)
NM_053025.3(MYLK):c.570G>T (p.Pro190=) rs56377408
NM_053025.3(MYLK):c.571C>G (p.Gln191Glu) rs794727880
NM_053025.3(MYLK):c.5742G>T (p.Glu1914Asp) rs1553768506
NM_053025.3(MYLK):c.588+10C>T rs886038709
NM_053025.3(MYLK):c.619G>A (p.Val207Met) rs756560698
NM_053025.3(MYLK):c.830A>G (p.Asn277Ser)
NM_053025.3(MYLK):c.992C>T (p.Thr331Met) rs371825849
NM_053027.3(MYLK):c.2596G>A (p.Gly866Ser) rs587782966
NM_053028.3(MYLK):c.3947G>A (p.Arg1316His)

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