Related gene-specific medical variations for Gene (Select 3290) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284840	NM_005525.4(HSD11B1):c.361A>G (p.Ile121Val)	HSD11B1, HSD11B1-AS1 (I121V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107072	NM_005525.4(HSD11B1):c.845C>T (p.Thr282Met)	HSD11B1, HSD11B1-AS1 (T282M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107071	NM_005525.4(HSD11B1):c.407T>A (p.Val136Glu)	HSD11B1, HSD11B1-AS1 (V136E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107070	NM_005525.4(HSD11B1):c.289A>T (p.Thr97Ser)	HSD11B1, HSD11B1-AS1 (T97S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107069	NM_005525.4(HSD11B1):c.262T>C (p.Tyr88His)	HSD11B1, HSD11B1-AS1 (Y88H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3048552	NM_005525.4(HSD11B1):c.165G>A (p.Ala55=)	HSD11B1, HSD11B1-AS1	Single nucleotide variant (synonymous variant)	HSD11B1-related disorder	GBenign
Select item 2627999	NM_005525.4(HSD11B1):c.678_679insT (p.Val227fs)	HSD11B1, HSD11B1-AS1 (V227fs)	Insertion (frameshift variant)	Exstrophy-epispadias complex	GUncertain significance
Select item 2608489	NM_005525.4(HSD11B1):c.647G>C (p.Gly216Ala)	HSD11B1, HSD11B1-AS1 (G216A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553534	NM_005525.4(HSD11B1):c.320G>C (p.Gly107Ala)	HSD11B1, HSD11B1-AS1 (G107A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483854	NM_005525.4(HSD11B1):c.29C>T (p.Pro10Leu)	HSD11B1, HSD11B1-AS1 (P10L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384299	NM_005525.4(HSD11B1):c.502G>A (p.Val168Ile)	HSD11B1, HSD11B1-AS1 (V168I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305550	NM_005525.4(HSD11B1):c.482G>A (p.Ser161Asn)	HSD11B1, HSD11B1-AS1 (S161N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295063	NM_005525.4(HSD11B1):c.707C>T (p.Ala236Val)	HSD11B1, HSD11B1-AS1 (A236V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1678195	NM_005525.4(HSD11B1):c.517+8G>A	HSD11B1, HSD11B1-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 787221	NM_005525.4(HSD11B1):c.518-9G>A	HSD11B1, HSD11B1-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 743453	NM_005525.4(HSD11B1):c.117C>T (p.Val39=)	HSD11B1, HSD11B1-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 435467	NM_005525.4(HSD11B1):c.744G>C (p.Gly248=)	HSD11B1, HSD11B1-AS1	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 375731	NM_005525.4(HSD11B1):c.331+53dup	HSD11B1, HSD11B1-AS1	Duplication (intron variant)	Cortisone reductase deficiency 2	GBenign
Select item 375729	NM_005525.4(HSD11B1):c.332-29T>G	HSD11B1-AS1, HSD11B1	Single nucleotide variant (intron variant)	Cortisone reductase deficiency 2 +1 more	GBenign
Select item 31589	NM_005525.4(HSD11B1):c.561G>T (p.Lys187Asn)	HSD11B1, HSD11B1-AS1 (K187N)	Single nucleotide variant (missense variant)	Cortisone reductase deficiency 2	GPathogenic
Select item 31588	NM_005525.4(HSD11B1):c.409C>T (p.Arg137Cys)	HSD11B1, HSD11B1-AS1 (R137C)	Single nucleotide variant (missense variant)	Cortisone reductase deficiency 2	GPathogenic
Select item 8911	NM_181755.2(HSD11B1):c.[331+53_331+54insA;332-29T>G]	HSD11B1-AS1, HSD11B1	Single nucleotide variant (intron variant)	Cortisone reductase deficiency 2	GUncertain significance

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Items: 22