"Ambry Genetics"[submitter] AND "LOC126860802"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 452493	NM_001370100.5(ZMYND11):c.1282C>T (p.Pro428Ser)	LOC126860802, ZMYND11 (P428S +15 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2322461	NM_001370100.5(ZMYND11):c.1375A>C (p.Asn459His)	LOC126860802, ZMYND11 (N302H +15 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2471280	NM_001370100.5(ZMYND11):c.1394G>A (p.Ser465Asn)	LOC126860802, ZMYND11 (S410N +15 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 1391336	NM_001370100.5(ZMYND11):c.1474C>T (p.Arg492Cys)	LOC126860802, ZMYND11 (R416C +15 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 2532450	NM_001370100.5(ZMYND11):c.1571T>C (p.Met524Thr)	LOC126860802, ZMYND11 (M405T +15 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2257739	NM_001370100.5(ZMYND11):c.1677_1686+38dup	LOC126860802, ZMYND11	Duplication (no sequence alteration +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar