List of variants in gene NACC1 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_052876.4(NACC1):c.1462G>A (p.Ala488Thr)	rs150928114	0.00199
NM_052876.4(NACC1):c.207G>A (p.Leu69=)	rs149110290	0.00119
NM_052876.4(NACC1):c.1386C>T (p.Asp462=)	rs147213591	0.00093
NM_052876.4(NACC1):c.1540A>G (p.Ser514Gly)	rs140644046	0.00072
NM_052876.4(NACC1):c.651C>T (p.His217=)	rs745755014	0.00009
NM_052876.4(NACC1):c.1128C>T (p.Asn376=)	rs544079071	0.00003
NM_052876.4(NACC1):c.-8-7C>T
NM_052876.4(NACC1):c.156C>T (p.Ser52=)
NM_052876.4(NACC1):c.282G>A (p.Val94=)	rs148939487
NM_052876.4(NACC1):c.335T>G (p.Ile112Ser)
NM_052876.4(NACC1):c.677C>T (p.Pro226Leu)
NM_052876.4(NACC1):c.735G>A (p.Gly245=)
NM_052876.4(NACC1):c.740CAG[2] (p.Ala249del)	rs777103054
NM_052876.4(NACC1):c.783G>A (p.Arg261=)	rs1257138098

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