"Revvity Omics, Revvity"[submitter] AND "GREB1L"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2432267	NM_001142966.3(GREB1L):c.203G>T (p.Arg68Leu)	LOC101927521, GREB1L (R68L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2432270	NM_001142966.3(GREB1L):c.226G>A (p.Asp76Asn)	GREB1L, LOC101927521 (D76N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2432266	NM_001142966.3(GREB1L):c.566G>A (p.Arg189Lys)	GREB1L, LOC101927521 (R189K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2440592	NM_001142966.3(GREB1L):c.1729C>T (p.Gln577Ter)	GREB1L, LOC101927521 (Q468* +2 more)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 2634686	NM_001142966.3(GREB1L):c.1901G>C (p.Ser634Thr)	GREB1L (S525T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2432269	NM_001142966.3(GREB1L):c.2938G>A (p.Asp980Asn)	GREB1L (D1023N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2432268	NM_001142966.3(GREB1L):c.5060G>T (p.Arg1687Met)	GREB1L (R1578M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar