ARB2A[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3235543	NM_032042.6(ARB2A):c.1159A>C (p.Lys387Gln)	ARB2A (K277Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235555	NM_032042.6(ARB2A):c.917G>A (p.Arg306Gln)	ARB2A (R196Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320131	NM_032042.6(ARB2A):c.868G>A (p.Val290Ile)	ARB2A (V244I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468413	NM_032042.6(ARB2A):c.848C>T (p.Ala283Val)	ARB2A (A283V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214866	NM_032042.6(ARB2A):c.835A>G (p.Ile279Val)	ARB2A (I233V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528685	NM_032042.6(ARB2A):c.774A>C (p.Gln258His)	ARB2A (Q212H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527838	NM_032042.6(ARB2A):c.684A>C (p.Glu228Asp)	ARB2A (E182D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540806	NM_032042.6(ARB2A):c.679C>G (p.Arg227Gly)	ARB2A (R117G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235552	NM_032042.6(ARB2A):c.676A>G (p.Lys226Glu)	ARB2A (K116E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235551	NM_032042.6(ARB2A):c.626C>T (p.Pro209Leu)	ARB2A (P163L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235550	NM_032042.6(ARB2A):c.585A>G (p.Ile195Met)	ARB2A (I149M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329381	NM_032042.6(ARB2A):c.411C>G (p.Ile137Met)	ARB2A (I137M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235549	NM_032042.6(ARB2A):c.404G>A (p.Ser135Asn)	ARB2A (S135N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235546	NM_032042.6(ARB2A):c.341A>G (p.Glu114Gly)	ARB2A (E114G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235545	NM_032042.6(ARB2A):c.314T>C (p.Ile105Thr)	ARB2A (I105T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289057	NM_032042.6(ARB2A):c.295G>A (p.Glu99Lys)	ARB2A (E99K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235544	NM_032042.6(ARB2A):c.166T>A (p.Phe56Ile)	ARB2A (F10I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3235553	NM_032042.6(ARB2A):c.78T>A (p.Asp26Glu)	ARB2A (D26E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3235547	NM_032042.6(ARB2A):c.37A>G (p.Ile13Val)	ARB2A (I13V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance