"Ambry Genetics"[submitter] AND "TTC7B-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2356759	NM_001010854.2(TTC7B):c.1726C>G (p.Leu576Val)	TTC7B, TTC7B-AS1 (L576V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383502	NM_001010854.2(TTC7B):c.1717G>A (p.Asp573Asn)	TTC7B, TTC7B-AS1 (D471N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372491	NM_001010854.2(TTC7B):c.1714A>G (p.Ile572Val)	TTC7B, TTC7B-AS1 (I470V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184395	NM_001010854.2(TTC7B):c.1601C>G (p.Ala534Gly)	TTC7B, TTC7B-AS1 (A432G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311868	NM_001010854.2(TTC7B):c.1579A>G (p.Ile527Val)	LOC126862023, TTC7B +1 more (I527V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2377766	NM_001010854.2(TTC7B):c.1565C>G (p.Ala522Gly)	LOC126862023, TTC7B +1 more (A420G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

ClinVar