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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9825	NM_000044.6(AR):c.178C>T (p.Gln60Ter)	AR, LOC109504725 (Q60*)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2439148	NM_000044.6(AR):c.194A>T (p.Gln65Leu)	AR, LOC109504725 (Q65L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2688588	NM_000044.6(AR):c.458C>T (p.Pro153Leu)	AR (P153L)	Single nucleotide variant (missense variant +1 more)	Kennedy disease +2 more	GConflicting classifications of pathogenicity
Select item 1323926	NM_000044.6(AR):c.649del (p.Ala217fs)	AR (A217fs)	Deletion (frameshift variant +1 more)	not provided	GLikely pathogenic
Select item 9819	NM_000044.6(AR):c.2324G>A (p.Arg775His)	AR (R243H +1 more)	Single nucleotide variant (missense variant)	Androgen resistance syndrome +2 more	GPathogenic
Select item 1025856	NM_000044.6(AR):c.2334G>T (p.Lys778Asn)	AR (K246N +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 9847	NM_000044.6(AR):c.2423T>C (p.Met808Thr)	AR (M276T +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 654813	NM_000044.6(AR):c.2678C>T (p.Pro893Leu)	AR (P893L +1 more)	Single nucleotide variant (missense variant)	Androgen resistance syndrome +2 more	GPathogenic/Likely pathogenic

ClinVar