ClinVar Miner

List of variants reported as not provided by Leiden Muscular Dystrophy (TPM1)

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Total variants: 32
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HGVS dbSNP
NM_001018005.2(TPM1):c.109A>G (p.Lys37Glu) rs199476303
NM_001018005.2(TPM1):c.118G>A (p.Glu40Lys) rs104894501
NM_001018005.2(TPM1):c.160G>A (p.Glu54Lys) rs104894505
NM_001018005.2(TPM1):c.172G>C (p.Asp58His) rs199476304
NM_001018005.2(TPM1):c.184G>C (p.Glu62Gln) rs199476305
NM_001018005.2(TPM1):c.188C>T (p.Ala63Val) rs199476306
NM_001018005.2(TPM1):c.209A>C (p.Lys70Thr) rs199476307
NM_001018005.2(TPM1):c.240+4470G>T rs199476308
NM_001018005.2(TPM1):c.241-12_241-11delinsTG rs199476309
NM_001018005.2(TPM1):c.275T>C (p.Ile92Thr) rs199476310
NM_001018005.2(TPM1):c.284T>C (p.Val95Ala) rs104894504
NM_001018005.2(TPM1):c.403C>A (p.Gln135Lys) rs11558749
NM_001018005.2(TPM1):c.453C>A (p.Ala151=) rs1071646
NM_001018005.2(TPM1):c.45G>T (p.Lys15Asn) rs199476301
NM_001018005.2(TPM1):c.479G>A (p.Arg160His) rs199476311
NM_001018005.2(TPM1):c.486T>C (p.Tyr162=) rs11558747
NM_001018005.2(TPM1):c.515T>C (p.Ile172Thr) rs199476312
NM_001018005.2(TPM1):c.523G>A (p.Asp175Asn) rs104894503
NM_001018005.2(TPM1):c.539A>G (p.Glu180Gly) rs104894502
NM_001018005.2(TPM1):c.539A>T (p.Glu180Val) rs104894502
NM_001018005.2(TPM1):c.549T>G (p.Ala183=) rs199476313
NM_001018005.2(TPM1):c.554T>G (p.Leu185Arg) rs199476314
NM_001018005.2(TPM1):c.574G>A (p.Glu192Lys) rs199476315
NM_001018005.2(TPM1):c.61= (p.Arg21=) rs1437698471
NM_001018005.2(TPM1):c.644C>T (p.Ser215Leu) rs199476316
NM_001018005.2(TPM1):c.67G>C (p.Glu23Gln) rs199476302
NM_001018005.2(TPM1):c.688G>A (p.Asp230Asn) rs199476317
NM_001018005.2(TPM1):c.715G>A (p.Ala239Thr) rs199476318
NM_001018005.2(TPM1):c.742A>G (p.Lys248Glu) rs199476319
NM_001018005.2(TPM1):c.830C>T (p.Ala277Val) rs199476320
NM_001018005.2(TPM1):c.842T>C (p.Met281Thr) rs199476321
NM_001018005.2(TPM1):c.850A>G (p.Ile284Val) rs199476322

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