List of variants in gene AP4M1 reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_004722.4(AP4M1):c.333A>C (p.Glu111Asp)	rs138437966	0.00066
NM_004722.4(AP4M1):c.380C>T (p.Thr127Met)	rs147261925	0.00023
NM_004722.4(AP4M1):c.1100G>A (p.Arg367Gln)	rs139861201	0.00021
NM_004722.4(AP4M1):c.673+7C>T	rs753446678	0.00003
NM_004722.4(AP4M1):c.1259A>G (p.Gln420Arg)
NM_004722.4(AP4M1):c.1321C>T (p.Arg441Ter)	rs886041126
NM_004722.4(AP4M1):c.58+3A>G	rs2116614199

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