List of variants in gene MICAL1 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_022765.4(MICAL1):c.2062C>A (p.His688Asn)	rs41288558	0.00618
NM_022765.4(MICAL1):c.1599G>A (p.Leu533=)	rs142979809	0.00219
NM_022765.4(MICAL1):c.2982-8C>T	rs199700552	0.00175
NM_022765.4(MICAL1):c.347G>A (p.Arg116His)	rs144411949	0.00175
NM_022765.4(MICAL1):c.571+1G>T	rs138930729	0.00036
NM_022765.4(MICAL1):c.2167C>T (p.Arg723Cys)	rs149976085	0.00026
NM_022765.4(MICAL1):c.1937G>A (p.Arg646Gln)	rs150285580	0.00004
NM_022765.4(MICAL1):c.2514C>T (p.Ser838=)	rs770153820	0.00004
NM_022765.4(MICAL1):c.1004G>A (p.Arg335Gln)
NM_022765.4(MICAL1):c.1063G>A (p.Ala355Thr)
NM_022765.4(MICAL1):c.1414C>T (p.Arg472Trp)
NM_022765.4(MICAL1):c.1578G>A (p.Pro526=)
NM_022765.4(MICAL1):c.1635C>T (p.Ala545=)
NM_022765.4(MICAL1):c.2291_2300del (p.Gly764fs)	rs1447618526
NM_022765.4(MICAL1):c.2348C>G (p.Ser783Ter)
NM_022765.4(MICAL1):c.422A>C (p.Lys141Thr)

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