"Ambry Genetics"[submitter] AND "IL1R2"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109240	NM_004633.4(IL1R2):c.16G>A (p.Val6Met)	IL1R2 (V6M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2553501	NM_004633.4(IL1R2):c.65C>G (p.Thr22Arg)	IL1R2 (T22R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109245	NM_004633.4(IL1R2):c.98G>A (p.Arg33Lys)	IL1R2 (R33K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2556497	NM_004633.4(IL1R2):c.179C>T (p.Ser60Phe)	IL1R2 (S60F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109241	NM_004633.4(IL1R2):c.263C>A (p.Ala88Asp)	IL1R2 (A88D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220764	NM_004633.4(IL1R2):c.271G>A (p.Gly91Ser)	IL1R2 (G91S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109242	NM_004633.4(IL1R2):c.359C>G (p.Ser120Cys)	IL1R2 (S120C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472050	NM_004633.4(IL1R2):c.401C>T (p.Pro134Leu)	IL1R2 (P134L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109243	NM_004633.4(IL1R2):c.416C>T (p.Pro139Leu)	IL1R2 (P139L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330885	NM_004633.4(IL1R2):c.479G>A (p.Arg160His)	IL1R2 (R160H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109244	NM_004633.4(IL1R2):c.616C>T (p.Arg206Cys)	IL1R2 (R206C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544002	NM_004633.4(IL1R2):c.637C>T (p.His213Tyr)	IL1R2 (H213Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461450	NM_004633.4(IL1R2):c.738A>G (p.Ile246Met)	IL1R2 (I246M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247750	NM_004633.4(IL1R2):c.779T>G (p.Val260Gly)	IL1R2 (V260G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463191	NM_004633.4(IL1R2):c.866G>A (p.Arg289His)	IL1R2 (R289H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361350	NM_004633.4(IL1R2):c.883C>T (p.Arg295Cys)	IL1R2 (R295C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109246	NM_004633.4(IL1R2):c.994C>A (p.Leu332Met)	IL1R2 (L332M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109237	NM_004633.4(IL1R2):c.1087G>A (p.Val363Ile)	IL1R2 (V363I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299023	NM_004633.4(IL1R2):c.1115G>A (p.Arg372Gln)	IL1R2 (R372Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109238	NM_004633.4(IL1R2):c.1144G>C (p.Gly382Arg)	IL1R2 (G382R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109239	NM_004633.4(IL1R2):c.1163C>A (p.Pro388His)	IL1R2 (P388H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 21