ASB13[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2537908	NM_024701.4(ASB13):c.806C>T (p.Pro269Leu)	ASB13 (P269L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479572	NM_024701.4(ASB13):c.752G>T (p.Arg251Met)	ASB13 (R251M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130105	NM_024701.4(ASB13):c.632G>A (p.Arg211Gln)	ASB13 (R211Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130104	NM_024701.4(ASB13):c.568G>T (p.Ala190Ser)	ASB13 (A190S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359144	NM_024701.4(ASB13):c.565G>A (p.Ala189Thr)	ASB13 (A189T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130103	NM_024701.4(ASB13):c.502G>A (p.Val168Met)	ASB13 (V168M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130102	NM_024701.4(ASB13):c.418G>A (p.Gly140Arg)	ASB13 (G140R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130101	NM_024701.4(ASB13):c.376A>C (p.Met126Leu)	ASB13 (M126L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130100	NM_024701.4(ASB13):c.371C>T (p.Ala124Val)	ASB13 (A124V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130099	NM_024701.4(ASB13):c.291C>G (p.Ser97Arg)	ASB13 (S97R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276158	NM_024701.4(ASB13):c.188G>A (p.Gly63Asp)	ASB13 (G63D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130106	NM_024701.4(ASB13):c.94A>T (p.Ser32Cys)	ASB13 (S32C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315285	NM_024701.4(ASB13):c.52G>T (p.Val18Leu)	ASB13 (V18L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance