ClinVar Miner

List of variants reported by National Institute of Mental Health and Neurosciences

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000159.4(GCDH):c.*165A>G rs8012 0.64188
NM_000159.4(GCDH):c.*288G>T rs9384 0.33464
NM_000159.4(GCDH):c.852+223C>T rs11085825 0.30906
NM_000159.4(GCDH):c.*340G>A rs190174770 0.00014
NM_000159.4(GCDH):c.885C>T (p.Tyr295=) rs139192015 0.00006
NM_000159.4(GCDH):c.*331T>C rs869025297
NM_000159.4(GCDH):c.*332C>A rs869025298
NM_000159.4(GCDH):c.1031C>T (p.Thr344Ile) rs869025299
NM_000159.4(GCDH):c.1114A>G (p.Arg372Gly) rs771924230
NM_000159.4(GCDH):c.1167_1168insT (p.Gly390fs) rs1568429257
NM_000159.4(GCDH):c.1173del (p.Asn392fs) rs754002357
NM_000159.4(GCDH):c.1240G>T (p.Glu414Ter) rs147611168
NM_000159.4(GCDH):c.296A>G (p.Glu99Gly) rs1294124984
NM_000159.4(GCDH):c.431A>C (p.Gln144Pro) rs878853154
NM_000159.4(GCDH):c.456C>G (p.Ile152Met) rs878853153
NM_000159.4(GCDH):c.675G>A (p.Trp225Ter) rs786205862
NM_000159.4(GCDH):c.701G>C (p.Arg234Pro) rs1203022386
NM_000159.4(GCDH):c.795_796insCTATGATCATC (p.Met266delinsLeuTer) rs869025300
NM_000159.4(GCDH):c.856C>T (p.Pro286Ser) rs786205861
NM_000159.4(GCDH):c.87G>A (p.Gln29=) rs878853155
NM_000159.4(GCDH):c.999G>A (p.Gln333=) rs878853156

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