"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ARV1"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 777986	NM_022786.3(ARV1):c.64A>T (p.Thr22Ser)	ARV1, LOC129932761 (T22S)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign/Likely benign
Select item 734292	NM_022786.3(ARV1):c.73G>T (p.Ala25Ser)	ARV1, LOC129932761 (A25S)	Single nucleotide variant (missense variant +1 more)	ARV1-related condition +1 more	GLikely benign
Select item 2640073	NM_022786.3(ARV1):c.81G>T (p.Ser27=)	ARV1, LOC129932761	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640074	NM_022786.3(ARV1):c.214G>A (p.Asp72Asn)	ARV1 (D72N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2640075	NM_022786.3(ARV1):c.295-5A>G	ARV1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3026922	NM_022786.3(ARV1):c.655A>C (p.Asn219His)	ARV1 (N219H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1176857	NM_022786.3(ARV1):c.732G>A (p.Leu244=)	ARV1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

ClinVar