"Ambry Genetics"[submitter] AND "IL17RE"[gene] - ClinVar

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Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2363904	NM_153480.2(IL17RE):c.-38G>A	IL17RE (C28Y)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2332941	NM_153480.2(IL17RE):c.-29T>C	IL17RE (V31A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3109182	NM_153480.2(IL17RE):c.3G>A (p.Met1Ile)	IL17RE (M1I +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2409945	NM_153480.2(IL17RE):c.55G>A (p.Asp19Asn)	IL17RE (D19N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109184	NM_153480.2(IL17RE):c.85C>T (p.Arg29Cys)	IL17RE (R29C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2242608	NM_153480.2(IL17RE):c.86G>A (p.Arg29His)	IL17RE (R69H +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 2537920	NM_153480.2(IL17RE):c.94C>A (p.Pro32Thr)	IL17RE (P32T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109185	NM_153480.2(IL17RE):c.107C>T (p.Thr36Ile)	IL17RE (T76I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2525757	NM_153480.2(IL17RE):c.137A>G (p.Asp46Gly)	IL17RE (D46G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285779	NM_153480.2(IL17RE):c.152G>A (p.Ser51Asn)	IL17RE (S51N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2392582	NM_153480.2(IL17RE):c.172C>T (p.Arg58Cys)	IL17RE (R98C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3285782	NM_153480.2(IL17RE):c.199A>G (p.Lys67Glu)	IL17RE (K67E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109186	NM_153480.2(IL17RE):c.215G>A (p.Arg72Gln)	IL17RE (R112Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2286289	NM_153480.2(IL17RE):c.286T>C (p.Phe96Leu)	IL17RE (F96L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109188	NM_153480.2(IL17RE):c.333C>A (p.Phe111Leu)	IL17RE (F151L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3285781	NM_153480.2(IL17RE):c.408T>A (p.His136Gln)	IL17RE (H136Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309352	NM_153480.2(IL17RE):c.421C>T (p.Pro141Ser)	IL17RE (P141S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109189	NM_153480.2(IL17RE):c.496C>A (p.Leu166Ile)	IL17RE (L206I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377634	NM_153480.2(IL17RE):c.563G>A (p.Arg188Gln)	IL17RE (R188Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292544	NM_153480.2(IL17RE):c.604G>A (p.Val202Met)	IL17RE (V202M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109190	NM_153480.2(IL17RE):c.665A>T (p.Gln222Leu)	IL17RE (Q222L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531199	NM_153480.2(IL17RE):c.680G>A (p.Gly227Glu)	IL17RE (G111E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109191	NM_153480.2(IL17RE):c.692T>C (p.Val231Ala)	IL17RE (V115A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295569	NM_153480.2(IL17RE):c.809C>T (p.Ser270Leu)	IL17RE (S154L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109192	NM_153480.2(IL17RE):c.835A>G (p.Thr279Ala)	IL17RE (T279A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493855	NM_153480.2(IL17RE):c.926G>C (p.Trp309Ser)	IL17RE (W349S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593586	NM_153480.2(IL17RE):c.932C>T (p.Thr311Ile)	IL17RE (T195I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109181	NM_153480.2(IL17RE):c.986T>C (p.Val329Ala)	IL17RE (V329A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273235	NM_153480.2(IL17RE):c.1232G>A (p.Arg411Gln)	IL17RE (R451Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2314807	NM_153480.2(IL17RE):c.1235G>A (p.Gly412Asp)	IL17RE (G296D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359669	NM_153480.2(IL17RE):c.1278G>T (p.Arg426Ser)	IL17RE (R310S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609632	NM_153480.2(IL17RE):c.1393C>G (p.Leu465Val)	IL17RE (L465V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264971	NM_153480.2(IL17RE):c.1409G>A (p.Gly470Asp)	IL17RE (G510D +2 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2550869	NM_153480.2(IL17RE):c.1467A>C (p.Pro489=)	IL17RE (S514R)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2543843	NM_153480.2(IL17RE):c.1471C>T (p.Leu491Phe)	IL17RE, LOC129936140 (L531F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244148	NM_153480.2(IL17RE):c.1474C>T (p.Leu492Phe)	IL17RE, LOC129936140 (L492F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464041	NM_153480.2(IL17RE):c.1508G>A (p.Arg503His)	IL17RE, LOC129936140 (R543H +2 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 3109183	NM_153480.2(IL17RE):c.1558C>T (p.Arg520Cys)	IL17RE (R520C +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2513025	NM_153480.2(IL17RE):c.1697C>G (p.Pro566Arg)	IL17RE, LOC129936141 (P450R +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2399839	NM_153480.2(IL17RE):c.1709C>T (p.Pro570Leu)	IL17RE, LOC129936141 (P454L +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2286828	NM_153480.2(IL17RE):c.1715C>T (p.Pro572Leu)	IL17RE, LOC129936141 (P612L +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2387472	NM_153480.2(IL17RE):c.1817C>T (p.Pro606Leu)	IL17RE (P646L +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3285780	NM_153480.2(IL17RE):c.1832C>T (p.Pro611Leu)	IL17RE (P611L +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2265122	NM_153480.2(IL17RE):c.1903A>T (p.Thr635Ser)	IL17RE, LOC129936142 (T519S +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2562964	NM_153480.2(IL17RE):c.1954C>G (p.Leu652Val)	IL17RE, LOC129936142 (L652V +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 45