"Genome-Nilou Lab"[submitter] AND "GEMIN4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1182789	NM_015721.3(GEMIN4):c.3097C>T (p.Arg1033Cys)	GEMIN4 (R1033C)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1185306	NM_015721.3(GEMIN4):c.2785G>A (p.Asp929Asn)	GEMIN4 (D929N)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1185307	NM_015721.3(GEMIN4):c.2216T>C (p.Ile739Thr)	GEMIN4 (I739T)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1185308	NM_015721.3(GEMIN4):c.2051G>A (p.Arg684Gln)	GEMIN4 (R684Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1185309	NM_015721.3(GEMIN4):c.1736C>G (p.Ala579Gly)	GEMIN4 (A579G)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1185310	NM_015721.3(GEMIN4):c.1348C>G (p.Gln450Glu)	GEMIN4 (Q450E)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1185311	NM_015721.3(GEMIN4):c.765C>T (p.Asp255=)	GEMIN4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1185312	NM_015721.3(GEMIN4):c.10+80C>T	GEMIN4, LOC130059866	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar