"Ambry Genetics"[submitter] AND "IL17RC"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 57

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 933528	NM_153460.4(IL17RC):c.41G>A (p.Arg14Gln)	IL17RC (R14Q)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1359308	NM_153460.4(IL17RC):c.69G>T (p.Arg23Ser)	IL17RC (R23S)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 581719	NM_153460.4(IL17RC):c.88G>T (p.Ala30Ser)	IL17RC (A30S)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2230650	NM_153460.4(IL17RC):c.105+33G>T	IL17RC (R46S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109165	NM_153460.4(IL17RC):c.105+52G>C	IL17RC (A53P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319079	NM_153460.4(IL17RC):c.105+119C>G	IL17RC (S75C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277213	NM_153460.4(IL17RC):c.105+131G>A	IL17RC (G79D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1060817	NM_153460.4(IL17RC):c.105+145C>T	IL17RC (R84W)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GConflicting classifications of pathogenicity
Select item 2618774	NM_153460.4(IL17RC):c.157A>G (p.Ile53Val)	IL17RC (I124V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1004864	NM_153460.4(IL17RC):c.160G>A (p.Val54Met)	IL17RC (V125M +1 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GConflicting classifications of pathogenicity
Select item 2218859	NM_153460.4(IL17RC):c.175C>G (p.Pro59Ala)	IL17RC (P59A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1357681	NM_153460.4(IL17RC):c.178G>A (p.Val60Met)	IL17RC (V60M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2379690	NM_153460.4(IL17RC):c.185C>T (p.Ala62Val)	IL17RC (A133V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 565492	NM_153460.4(IL17RC):c.274G>T (p.Val92Leu)	IL17RC (V163L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2309471	NM_153460.4(IL17RC):c.298G>A (p.Glu100Lys)	IL17RC (E100K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 643162	NM_153460.4(IL17RC):c.376G>A (p.Val126Met)	IL17RC (V197M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 998838	NM_153460.4(IL17RC):c.406C>T (p.Arg136Cys)	IL17RC (R111C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2235133	NM_153460.4(IL17RC):c.578A>G (p.Asp193Gly)	IL17RC (D264G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396437	NM_153460.4(IL17RC):c.586G>T (p.Gly196Trp)	IL17RC (G267W +1 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 570464	NM_153460.4(IL17RC):c.587G>T (p.Gly196Val)	IL17RC (G267V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2290431	NM_153460.4(IL17RC):c.666T>A (p.His222Gln)	IL17RC (H222Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1447457	NM_153460.4(IL17RC):c.687G>C (p.Glu229Asp)	IL17RC (E189D +3 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2844463	NM_153460.4(IL17RC):c.728A>C (p.Gln243Pro)	IL17RC (Q203P +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 1062758	NM_153460.4(IL17RC):c.737C>A (p.Pro246Gln)	IL17RC (P206Q +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 2084207	NM_153460.4(IL17RC):c.745C>T (p.Arg249Trp)	IL17RC (R249W +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2152840	NM_153460.4(IL17RC):c.754A>G (p.Lys252Glu)	IL17RC (K237E +3 more)	Single nucleotide variant (missense variant +2 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2788993	NM_153460.4(IL17RC):c.757A>C (p.Asn253His)	IL17RC (N238H +3 more)	Single nucleotide variant (missense variant +2 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2609526	NM_153460.4(IL17RC):c.811C>T (p.Leu271Phe)	IL17RC (L271F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 849815	NM_153460.4(IL17RC):c.823G>A (p.Val275Met)	IL17RC (V235M +4 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +2 more	GUncertain significance
Select item 2103030	NM_153460.4(IL17RC):c.874G>A (p.Glu292Lys)	IL17RC (E292K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 664224	NM_153460.4(IL17RC):c.883C>T (p.Arg295Cys)	IL17RC (R295C +4 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +2 more	GUncertain significance
Select item 1371542	NM_153460.4(IL17RC):c.914G>A (p.Arg305Gln)	IL17RC (R265Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 665792	NM_153460.4(IL17RC):c.991C>T (p.Arg331Trp)	IL17RC (R331W +4 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2311310	NM_153460.4(IL17RC):c.1072T>A (p.Phe358Ile)	IL17RC (F429I +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 542530	NM_153460.4(IL17RC):c.1099C>G (p.Leu367Val)	IL17RC (L438V +4 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 1503651	NM_153460.4(IL17RC):c.1121C>T (p.Ser374Leu)	IL17RC (S334L +6 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1495067	NM_153460.4(IL17RC):c.1240C>T (p.Pro414Ser)	IL17RC (P374S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2287175	NM_153460.4(IL17RC):c.1312G>T (p.Asp438Tyr)	IL17RC (D406Y +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109163	NM_153460.4(IL17RC):c.1314C>A (p.Asp438Glu)	IL17RC (D406E +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109164	NM_153460.4(IL17RC):c.1325G>A (p.Gly442Asp)	IL17RC (G427D +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 475923	NM_153460.4(IL17RC):c.1439C>T (p.Ala480Val)	IL17RC (A551V +6 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 648232	NM_153460.4(IL17RC):c.1471G>A (p.Asp491Asn)	IL17RC (D459N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1429834	NM_153460.4(IL17RC):c.1519G>A (p.Gly507Arg)	IL17RC, LOC129936143 (G507R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 944363	NM_153460.4(IL17RC):c.1519G>C (p.Gly507Arg)	IL17RC, LOC129936143 (G475R +3 more)	Single nucleotide variant (missense variant +2 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2475034	NM_153460.4(IL17RC):c.1617G>C (p.Gln539His)	IL17RC (Q507H +9 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 3014433	NM_153460.4(IL17RC):c.1681G>A (p.Ala561Thr)	IL17RC (A529T +9 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 850104	NM_153460.4(IL17RC):c.1703G>T (p.Arg568Leu)	IL17RC (R536L +8 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2054607	NM_153460.4(IL17RC):c.1867G>A (p.Gly623Ser)	IL17RC (G591S +9 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 3109166	NM_153460.4(IL17RC):c.1873G>A (p.Ala625Thr)	IL17RC (A580T +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 966925	NM_153460.4(IL17RC):c.1948G>C (p.Val650Leu)	IL17RC (V618L +8 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GUncertain significance
Select item 2201268	NM_153460.4(IL17RC):c.2057G>A (p.Arg686Gln)	IL17RC, LOC129936144 (R633Q +9 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GConflicting classifications of pathogenicity
Select item 3285774	NM_153460.4(IL17RC):c.2059G>T (p.Ala687Ser)	IL17RC, LOC129936144 (A634S +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2996418	NM_153460.4(IL17RC):c.2107G>A (p.Ala703Thr)	IL17RC, LOC129936144 (A677T +9 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1518140	NM_153460.4(IL17RC):c.2137G>A (p.Gly713Arg)	IL17RC, LOC129936144 (G660R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 542529	NM_153460.4(IL17RC):c.2144G>A (p.Gly715Glu)	IL17RC, LOC129936144 (G786E +8 more)	Single nucleotide variant (missense variant +1 more)	Candidiasis, familial, 9 +1 more	GConflicting classifications of pathogenicity
Select item 567761	NM_153460.4(IL17RC):c.2152G>A (p.Asp718Asn)	IL17RC, LOC129936144 (D789N +8 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2383051	NM_153460.4(IL17RC):c.2155G>C (p.Gly719Arg)	IL17RC, LOC129936144 (G693R +9 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 57