"Ambry Genetics"[submitter] AND "IL20RA"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2405063	NM_014432.4(IL20RA):c.1637G>C (p.Gly546Ala)	IL20RA (G413A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109293	NM_014432.4(IL20RA):c.1628A>G (p.Glu543Gly)	IL20RA (E432G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109292	NM_014432.4(IL20RA):c.1558A>G (p.Arg520Gly)	IL20RA (R387G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344792	NM_014432.4(IL20RA):c.1537G>A (p.Gly513Arg)	IL20RA (G402R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468470	NM_014432.4(IL20RA):c.1498G>A (p.Asp500Asn)	IL20RA (D451N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509160	NM_014432.4(IL20RA):c.1355C>G (p.Pro452Arg)	IL20RA (P341R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109289	NM_014432.4(IL20RA):c.1340A>G (p.Gln447Arg)	IL20RA (Q314R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464035	NM_014432.4(IL20RA):c.1289C>T (p.Thr430Ile)	IL20RA (T297I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457841	NM_014432.4(IL20RA):c.1286G>A (p.Gly429Glu)	IL20RA (G429E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330666	NM_014432.4(IL20RA):c.1222A>T (p.Thr408Ser)	IL20RA (T408S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390798	NM_014432.4(IL20RA):c.1181C>T (p.Pro394Leu)	IL20RA (P261L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593698	NM_014432.4(IL20RA):c.1120G>A (p.Glu374Lys)	IL20RA (E241K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539262	NM_014432.4(IL20RA):c.1106T>G (p.Ile369Ser)	IL20RA (I258S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333573	NM_014432.4(IL20RA):c.962A>G (p.Lys321Arg)	IL20RA (K321R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109297	NM_014432.4(IL20RA):c.836T>C (p.Val279Ala)	IL20RA (V168A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243559	NM_014432.4(IL20RA):c.705G>T (p.Gln235His)	IL20RA (Q102H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512856	NM_014432.4(IL20RA):c.679C>T (p.Arg227Cys)	IL20RA (R116C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224641	NM_014432.4(IL20RA):c.664G>A (p.Val222Ile)	IL20RA (V111I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109296	NM_014432.4(IL20RA):c.632A>G (p.Asn211Ser)	IL20RA (N100S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109295	NM_014432.4(IL20RA):c.343A>G (p.Ile115Val)	IL20RA (I115V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310027	NM_014432.4(IL20RA):c.278C>G (p.Thr93Ser)	IL20RA (T44S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558840	NM_014432.4(IL20RA):c.277A>G (p.Thr93Ala)	IL20RA (T44A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109294	NM_014432.4(IL20RA):c.268A>G (p.Ile90Val)	IL20RA (I90V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308833	NM_014432.4(IL20RA):c.206A>T (p.Tyr69Phe)	IL20RA, LOC132089353 (Y69F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569128	NM_014432.4(IL20RA):c.170C>T (p.Thr57Ile)	IL20RA, LOC132089353 (T57I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285827	NM_014432.4(IL20RA):c.131C>T (p.Thr44Ile)	IL20RA, LOC132089353 (T44I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2521572	NM_014432.4(IL20RA):c.55C>A (p.Leu19Met)	IL20RA, LOC129997246 (L19M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2618391	NM_014432.4(IL20RA):c.47C>T (p.Pro16Leu)	IL20RA, LOC129997246 (P16L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2213745	NM_014432.4(IL20RA):c.44C>A (p.Pro15Gln)	IL20RA, LOC129997246 (P15Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 29