"Ambry Genetics"[submitter] AND "LOC130058985"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2534391	NM_001365324.3(TENT4B):c.356G>C (p.Gly119Ala)	LOC130058985, TENT4B (G99A +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3325384	NM_001365324.3(TENT4B):c.403G>C (p.Ala135Pro)	LOC130058985, TENT4B (A120P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325385	NM_001365324.3(TENT4B):c.416C>T (p.Pro139Leu)	LOC130058985, TENT4B (P139L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325383	NM_001365324.3(TENT4B):c.421C>T (p.Pro141Ser)	LOC130058985, TENT4B (P126S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3176032	NM_001365324.3(TENT4B):c.449C>T (p.Pro150Leu)	LOC130058985, TENT4B (P135L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176033	NM_001365324.3(TENT4B):c.472A>G (p.Ser158Gly)	LOC130058985, TENT4B (S143G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176034	NM_001365324.3(TENT4B):c.520T>C (p.Tyr174His)	LOC130058985, TENT4B (Y174H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar