List of variants in gene CLP1 reported as uncertain significance for central nervous system malformation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006831.3(CLP1):c.178G>T (p.Gly60Cys)	rs200305079	0.00011
NM_006831.3(CLP1):c.310C>G (p.Arg104Gly)	rs994445804	0.00002
NM_006831.3(CLP1):c.427C>T (p.Arg143Cys)	rs957840738	0.00001
NM_006831.3(CLP1):c.1214C>T (p.Ala405Val)
NM_006831.3(CLP1):c.159_161del (p.Lys54del)	rs758902215
NM_006831.3(CLP1):c.293C>G (p.Thr98Arg)
NM_006831.3(CLP1):c.422T>A (p.Leu141Ter)	rs1945858355
NM_006831.3(CLP1):c.784C>G (p.Leu262Val)	rs952926202

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