"Eurofins Ntd Llc (ga)"[submitter] AND "HGF"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 289922	NM_000601.6(HGF):c.2019T>C (p.Tyr673=)	HGF	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 194607	NM_000601.6(HGF):c.1832G>C (p.Ser611Thr)	HGF (S611T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 194608	NM_000601.6(HGF):c.1814C>T (p.Thr605Ile)	HGF (T605I +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 593391	NM_000601.6(HGF):c.1675G>A (p.Glu559Lys)	HGF (E559K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 43606	NM_000601.6(HGF):c.1008G>A (p.Glu336=)	HGF	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 43611	NM_000601.6(HGF):c.910G>A (p.Glu304Lys)	HGF (E304K +1 more)	Single nucleotide variant (missense variant)	Nonsyndromic Hearing Loss, Mixed +2 more	GBenign/Likely benign
Select item 597018	NM_000601.6(HGF):c.717A>G (p.Thr239=)	HGF	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 196285	NM_000601.6(HGF):c.270T>C (p.Asp90=)	HGF	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity

ClinVar