C0039585[trait identifier] AND "Mendelics"[submitter] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 958035	NM_000044.6(AR):c.161TGC[5] (p.Leu57dup)	AR	Microsatellite (inframe_insertion +1 more)	Malignant tumor of prostate +2 more	GPathogenic
Select item 434257	NM_000044.6(AR):c.171GCA[24] (p.Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Kennedy disease +3 more	GBenign/Likely benign
Select item 804018	NM_000044.6(AR):c.528C>A (p.Ser176Arg)	AR (S176R)	Single nucleotide variant (missense variant +1 more)	AR-related condition +6 more	GBenign/Likely benign
Select item 1685533	NM_000044.6(AR):c.1063G>C (p.Glu355Gln)	AR (E355Q)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate +2 more	GConflicting classifications of pathogenicity
Select item 216890	NM_000044.6(AR):c.1174C>T (p.Pro392Ser)	AR (P392S)	Single nucleotide variant (missense variant +1 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 1167626	NM_000044.6(AR):c.1301C>T (p.Ser434Phe)	AR (S434F)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +4 more	GConflicting classifications of pathogenicity
Select item 804019	NM_000044.6(AR):c.1424C>T (p.Ala475Val)	AR (A475V)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +5 more	GConflicting classifications of pathogenicity
Select item 1685538	NM_000044.6(AR):c.1644G>T (p.Leu548Phe)	AR (L16F +1 more)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1685539	NM_000044.6(AR):c.1651G>C (p.Asp551His)	AR (D19H +1 more)	Single nucleotide variant (missense variant +1 more)	Androgen resistance syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1244234	NM_000044.6(AR):c.1792A>G (p.Ser598Gly)	AR (Q570R +2 more)	Single nucleotide variant (missense variant)	Male infertility +4 more	GConflicting classifications of pathogenicity
Select item 254736	NM_000044.6(AR):c.1886-60G>A	AR	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1686481	NM_000044.6(AR):c.1960G>A (p.Glu654Lys)	AR (E122K +1 more)	Single nucleotide variant (missense variant)	Androgen resistance syndrome +2 more	GBenign
Select item 9849	NM_000044.6(AR):c.2180G>T (p.Arg727Leu)	AR (R195L +1 more)	Single nucleotide variant (missense variant)	Androgen resistance syndrome +2 more	GConflicting classifications of pathogenicity
Select item 9817	NM_000044.6(AR):c.2191G>A (p.Val731Met)	AR (V199M +1 more)	Single nucleotide variant (missense variant)	Androgen resistance syndrome +2 more	GConflicting classifications of pathogenicity
Select item 9846	NM_000044.6(AR):c.2395C>G (p.Gln799Glu)	AR (Q267E +1 more)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity