IL22RA2[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 3109331	NM_052962.3(IL22RA2):c.775T>C (p.Cys259Arg)	IL22RA2 (C259R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543406	NM_052962.3(IL22RA2):c.737C>T (p.Pro246Leu)	IL22RA2 (P214L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109330	NM_052962.3(IL22RA2):c.734A>G (p.Gln245Arg)	IL22RA2 (Q213R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285842	NM_052962.3(IL22RA2):c.729A>G (p.Ile243Met)	IL22RA2 (I211M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558368	NM_052962.3(IL22RA2):c.697C>T (p.Pro233Ser)	IL22RA2 (P201S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109329	NM_052962.3(IL22RA2):c.683T>C (p.Ile228Thr)	IL22RA2 (I228T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620092	NM_052962.3(IL22RA2):c.676G>T (p.Val226Phe)	IL22RA2 (V226F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544877	NM_052962.3(IL22RA2):c.674C>T (p.Ala225Val)	IL22RA2 (A225V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2477867	NM_052962.3(IL22RA2):c.470A>C (p.Glu157Ala)	IL22RA2 (E125A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381885	NM_052962.3(IL22RA2):c.452G>A (p.Arg151Gln)	IL22RA2 (R119Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402289	NM_052962.3(IL22RA2):c.449C>T (p.Pro150Leu)	IL22RA2 (P150L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316998	NM_052962.3(IL22RA2):c.410C>T (p.Ala137Val)	IL22RA2 (A105V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109328	NM_052962.3(IL22RA2):c.397G>A (p.Gly133Arg)	IL22RA2 (G101R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285843	NM_052962.3(IL22RA2):c.389C>T (p.Pro130Leu)	IL22RA2 (P130L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109327	NM_052962.3(IL22RA2):c.158T>A (p.Leu53His)	IL22RA2 (L53H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357330	NM_052962.3(IL22RA2):c.116G>A (p.Arg39Gln)	IL22RA2 (R39Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1321338	NM_052962.3(IL22RA2):c.115C>T (p.Arg39Ter)	IL22RA2 (R39*)	Single nucleotide variant (nonsense)	Multisystem inflammatory syndrome in children	Grisk factor
Select item 2236620	NM_052962.3(IL22RA2):c.107T>A (p.Phe36Tyr)	IL22RA2 (F36Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336343	NM_052962.3(IL22RA2):c.77A>G (p.His26Arg)	IL22RA2 (H26R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance