List of variants in gene AP2M1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004068.4(AP2M1):c.423+7G>A	rs115561047	0.00230
NM_004068.4(AP2M1):c.1182C>T (p.Phe394=)	rs202236381	0.00064
NM_004068.4(AP2M1):c.237C>T (p.Phe79=)	rs11539598	0.00041
NM_004068.4(AP2M1):c.438A>G (p.Glu146=)	rs550065852	0.00006
NM_004068.4(AP2M1):c.1023G>A (p.Lys341=)	rs189182155	0.00002
NM_004068.4(AP2M1):c.1054G>A (p.Val352Met)
NM_004068.4(AP2M1):c.1242C>T (p.Ser414=)
NM_004068.4(AP2M1):c.423+4C>A	rs372570685
NM_004068.4(AP2M1):c.75-643G>A
NM_004068.4(AP2M1):c.963+8C>T

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