List of variants in gene NCAPH studied for microcephaly 23, primary, autosomal recessive

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_015341.5(NCAPH):c.1616T>C (p.Val539Ala)	rs2305935	0.30067
NM_015341.5(NCAPH):c.1131T>C (p.Asp377=)	rs3731935	0.20690
NM_015341.5(NCAPH):c.1867G>A (p.Ala623Thr)	rs111936698	0.00106
NM_015341.5(NCAPH):c.1952T>C (p.Met651Thr)	rs2064714077	0.00001
NM_015341.5(NCAPH):c.19+1G>C
NM_015341.5(NCAPH):c.728C>T (p.Pro243Leu)	rs1553446603

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