ClinVar Miner

List of variants in gene VCP reported as uncertain significance by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_007126.5(VCP):c.1584C>T (p.Ala528=) rs147623367 0.00064
NM_007126.5(VCP):c.954C>T (p.Gly318=) rs377316335 0.00018
NM_007126.5(VCP):c.811+2T>C rs539851936 0.00012
NM_007126.5(VCP):c.340A>G (p.Ile114Val) rs549915384 0.00009
NM_007126.5(VCP):c.1194+3G>A rs183223259 0.00008
NM_007126.5(VCP):c.1242G>A (p.Leu414=) rs375262833 0.00004
NM_007126.5(VCP):c.2121T>G (p.Ile707Met) rs1000496477 0.00003
NM_007126.5(VCP):c.1863C>T (p.Gly621=) rs376510669 0.00002
NM_007126.5(VCP):c.426G>A (p.Ala142=) rs577812326 0.00001
NM_007126.5(VCP):c.1121C>A (p.Ala374Asp) rs886043471
NM_007126.5(VCP):c.1156A>G (p.Lys386Glu) rs1563977665
NM_007126.5(VCP):c.1197A>G (p.Val399=) rs886044575
NM_007126.5(VCP):c.1433A>G (p.Asp478Gly) rs1554668345
NM_007126.5(VCP):c.1483-5C>T rs760031814
NM_007126.5(VCP):c.1488T>C (p.Pro496=) rs1563976866
NM_007126.5(VCP):c.1896C>A (p.Ala632=) rs141275388
NM_007126.5(VCP):c.1929C>T (p.Ile643=) rs1554668168
NM_007126.5(VCP):c.2283C>T (p.Thr761=) rs758596783
NM_007126.5(VCP):c.258A>G (p.Arg86=) rs1563980979
NM_007126.5(VCP):c.284G>C (p.Arg95Pro) rs758169026
NM_007126.5(VCP):c.555A>C (p.Glu185Asp) rs1333833979

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