Related gene-specific medical variations for Gene (Select 100505635) - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3079863	NM_001201427.2(DAAM2):c.2599C>T (p.Pro867Ser)	DAAM2, DAAM2-AS1 (P867S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3079862	NM_001201427.2(DAAM2):c.2578C>T (p.Pro860Ser)	DAAM2, DAAM2-AS1 (P860S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3059968	NM_001201427.2(DAAM2):c.2484C>T (p.Ile828=)	DAAM2, DAAM2-AS1	Single nucleotide variant (synonymous variant)	DAAM2-related condition	GBenign
Select item 3059909	NM_001201427.2(DAAM2):c.2607T>C (p.Ala869=)	DAAM2, DAAM2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DAAM2-related condition	GBenign
Select item 3050220	NM_001201427.2(DAAM2):c.2327A>C (p.Lys776Thr)	DAAM2, DAAM2-AS1 (K776T)	Single nucleotide variant (non-coding transcript variant +1 more)	DAAM2-related condition	GLikely benign
Select item 3044201	NM_001201427.2(DAAM2):c.2258A>G (p.Asp753Gly)	DAAM2, DAAM2-AS1 (D753G)	Single nucleotide variant (non-coding transcript variant +1 more)	DAAM2-related condition	GLikely benign
Select item 3042452	NM_001201427.2(DAAM2):c.2342-10C>T	DAAM2, DAAM2-AS1	Single nucleotide variant (intron variant)	DAAM2-related condition	GLikely benign
Select item 3038271	NM_001201427.2(DAAM2):c.2567T>C (p.Ile856Thr)	DAAM2, DAAM2-AS1 (I856T)	Single nucleotide variant (non-coding transcript variant +1 more)	DAAM2-related condition	GLikely benign
Select item 2622497	NM_001201427.2(DAAM2):c.2491A>G (p.Thr831Ala)	DAAM2, DAAM2-AS1 (T831A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2606028	NM_001201427.2(DAAM2):c.2323G>C (p.Ala775Pro)	DAAM2, DAAM2-AS1 (A775P)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2582484	NM_001201427.2(DAAM2):c.2279A>G (p.Gln760Arg)	DAAM2, DAAM2-AS1 (Q760R)	Single nucleotide variant (non-coding transcript variant +1 more)	Nephrotic syndrome, type 24	GUncertain significance
Select item 2582404	NM_001201427.2(DAAM2):c.2203G>A (p.Glu735Lys)	DAAM2, DAAM2-AS1 (E735K)	Single nucleotide variant (missense variant)	Nephrotic syndrome, type 24	GUncertain significance
Select item 2554664	NM_001201427.2(DAAM2):c.2446G>A (p.Gly816Ser)	DAAM2, DAAM2-AS1 (G816S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533016	NM_001201427.2(DAAM2):c.2578C>G (p.Pro860Ala)	DAAM2, DAAM2-AS1 (P860A)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2519736	NM_001201427.2(DAAM2):c.2222G>A (p.Arg741His)	DAAM2, DAAM2-AS1 (R741H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351935	NM_001201427.2(DAAM2):c.2380C>T (p.Arg794Cys)	DAAM2, DAAM2-AS1 (R794C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2327549	NM_001201427.2(DAAM2):c.2372G>A (p.Arg791His)	DAAM2, DAAM2-AS1 (R791H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2320777	NM_001201427.2(DAAM2):c.2512A>C (p.Asn838His)	DAAM2, DAAM2-AS1 (N838H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2276348	NM_001201427.2(DAAM2):c.2473C>T (p.Leu825Phe)	DAAM2, DAAM2-AS1 (L825F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 780622	NM_001201427.2(DAAM2):c.2510+8C>T	DAAM2, DAAM2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign

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Items: 20