"Ambry Genetics"[submitter] AND "IL25"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2556691	NM_172314.2(IL25):c.44A>C (p.His15Pro)	IL25 (H15P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206167	NM_172314.2(IL25):c.55C>T (p.His19Tyr)	IL25 (H19Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203934	NM_172314.2(IL25):c.65G>A (p.Ser22Asn)	IL25 (S22N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285847	NM_172314.2(IL25):c.106C>A (p.Leu36Met)	IL25 (L36M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109339	NM_172314.2(IL25):c.121G>C (p.Val41Leu)	IL25 (V41L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285846	NM_172314.2(IL25):c.157C>T (p.Arg53Cys)	IL25 (R53C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109340	NM_172314.2(IL25):c.170C>A (p.Ser57Tyr)	IL25 (S57Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109341	NM_172314.2(IL25):c.241G>T (p.Asp81Tyr)	IL25 (D81Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241620	NM_172314.2(IL25):c.265C>G (p.Leu89Val)	IL25 (L105V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109342	NM_172314.2(IL25):c.277C>T (p.Arg93Cys)	IL25 (R93C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391621	NM_172314.2(IL25):c.349C>G (p.Leu117Val)	IL25 (L133V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293240	NM_172314.2(IL25):c.382C>G (p.Pro128Ala)	IL25 (P144A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463290	NM_172314.2(IL25):c.394G>A (p.Glu132Lys)	IL25 (E132K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2241330	NM_172314.2(IL25):c.410A>G (p.Lys137Arg)	IL25 (K137R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295733	NM_172314.2(IL25):c.428G>T (p.Arg143Leu)	IL25 (R143L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330582	NM_172314.2(IL25):c.440G>A (p.Arg147His)	IL25 (R147H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211994	NM_172314.2(IL25):c.458T>C (p.Val153Ala)	IL25 (V153A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109343	NM_172314.2(IL25):c.467G>A (p.Arg156Gln)	IL25 (R156Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance