"Ambry Genetics"[submitter] AND "IL36G"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109413	NM_019618.4(IL36G):c.38G>C (p.Arg13Thr)	IL36G (R13T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554874	NM_019618.4(IL36G):c.92A>C (p.Asn31Thr)	IL36G (N31T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489134	NM_019618.4(IL36G):c.140G>A (p.Arg47Gln)	IL36G (R47Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399283	NM_019618.4(IL36G):c.178A>G (p.Thr60Ala)	IL36G (T25A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109411	NM_019618.4(IL36G):c.184A>G (p.Lys62Glu)	IL36G (K62E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324143	NM_019618.4(IL36G):c.217G>A (p.Asp73Asn)	IL36G (D73N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354904	NM_019618.4(IL36G):c.259T>C (p.Tyr87His)	IL36G (Y87H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109412	NM_019618.4(IL36G):c.340G>A (p.Val114Met)	IL36G (V114M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530775	NM_019618.4(IL36G):c.361C>T (p.Arg121Cys)	IL36G (R121C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109414	NM_019618.4(IL36G):c.419T>C (p.Ile140Thr)	IL36G (I140T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance