"Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan"[submitte - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688539	NM_021258.4(IL22RA1):c.*81C>T	IL22RA1, LOC122056794	Single nucleotide variant (3 prime UTR variant)	not specified	GBenign
Select item 2688377	NM_021258.4(IL22RA1):c.1552C>G (p.Arg518Gly)	IL22RA1 (R518G)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 2688433	NM_021258.4(IL22RA1):c.936C>T (p.Pro312=)	IL22RA1	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688472	NM_021258.4(IL22RA1):c.613G>A (p.Val205Ile)	IL22RA1 (V205I)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 2688374	NM_021258.4(IL22RA1):c.435A>C (p.Pro145=)	IL22RA1	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688450	NM_021258.4(IL22RA1):c.355+58G>A	IL22RA1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688503	NM_021258.4(IL22RA1):c.177-55G>A	IL22RA1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688368	NM_021258.4(IL22RA1):c.135G>A (p.Pro45=)	IL22RA1	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688372	NM_021258.4(IL22RA1):c.44-105G>A	IL22RA1	Single nucleotide variant (intron variant)	not specified	GBenign

ClinVar