CARD9[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 365830	NM_052813.5(CARD9):c.*139G>A	CARD9	Single nucleotide variant (splice acceptor variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 365831	NM_052813.5(CARD9):c.*130G>A	CARD9	Single nucleotide variant (3 prime UTR variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 914319	NM_052813.5(CARD9):c.*57C>T	CARD9	Single nucleotide variant (3 prime UTR variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 632538	NM_052813.5(CARD9):c.1609T>C (p.Ter537Gln)	CARD9	Single nucleotide variant (stop lost +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1907523	NM_052813.5(CARD9):c.1605C>T (p.Gly535=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 2182479	NM_052813.5(CARD9):c.1598C>T (p.Thr533Ile)	CARD9 (T533I)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 467796	NM_052813.5(CARD9):c.1596C>T (p.Asp532=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency +1 more	GBenign/Likely benign
Select item 2894330	NM_052813.5(CARD9):c.1593C>T (p.Thr531=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1996192	NM_052813.5(CARD9):c.1592C>T (p.Thr531Ile)	CARD9 (T531I)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 841108	NM_052813.5(CARD9):c.1586ACA[1] (p.Asn530del)	CARD9 (N530del)	Microsatellite (inframe_deletion +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2179651	NM_052813.5(CARD9):c.1590C>T (p.Asn530=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 799048	NM_052813.5(CARD9):c.1578G>A (p.Thr526=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1461407	NM_052813.5(CARD9):c.1577C>G (p.Thr526Arg)	CARD9 (T526R)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1517165	NM_052813.5(CARD9):c.1576A>G (p.Thr526Ala)	CARD9 (T526A)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 976604	NM_052813.5(CARD9):c.1574C>T (p.Thr525Ile)	CARD9 (T525I)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 535814	NM_052813.5(CARD9):c.1571A>C (p.Asn524Thr)	CARD9 (N524T)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency +1 more	GUncertain significance
Select item 646780	NM_052813.5(CARD9):c.1567G>C (p.Glu523Gln)	CARD9 (E523Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1036833	NM_052813.5(CARD9):c.1565G>A (p.Arg522Gln)	CARD9 (R522Q)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency +1 more	GConflicting classifications of pathogenicity
Select item 1509981	NM_052813.5(CARD9):c.1563C>G (p.Asp521Glu)	CARD9 (D521E)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1476736	NM_052813.5(CARD9):c.1554GGA[2] (p.Glu520del)	CARD9 (E520del)	Microsatellite (inframe_deletion +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1345984	NM_052813.5(CARD9):c.1562A>C (p.Asp521Ala)	CARD9 (D521A)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2135129	NM_052813.5(CARD9):c.1561G>C (p.Asp521His)	CARD9 (D521H)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1922685	NM_052813.5(CARD9):c.1561G>A (p.Asp521Asn)	CARD9 (D521N)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1034644	NM_052813.5(CARD9):c.1552G>T (p.Gly518Trp)	CARD9 (G518W)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2143178	NM_052813.5(CARD9):c.1551G>C (p.Gln517His)	CARD9 (Q517H)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 709540	NM_052813.5(CARD9):c.1551G>A (p.Gln517=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 858155	NM_052813.5(CARD9):c.1546C>T (p.Arg516Trp)	CARD9 (R516W)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1345605	NM_052813.5(CARD9):c.1545G>A (p.Trp515Ter)	CARD9 (W515*)	Single nucleotide variant (nonsense +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1015140	NM_052813.5(CARD9):c.1541G>C (p.Gly514Ala)	CARD9 (G514A)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1431821	NM_052813.5(CARD9):c.1540G>A (p.Gly514Arg)	CARD9 (G514R)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency +1 more	GUncertain significance
Select item 1554506	NM_052813.5(CARD9):c.1536G>A (p.Gln512=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 2889459	NM_052813.5(CARD9):c.1530G>A (p.Lys510=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency +1 more	GLikely benign
Select item 1936440	NM_052813.5(CARD9):c.1526G>A (p.Arg509Lys)	CARD9 (R509K)	Single nucleotide variant (intron variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2474438	NM_052813.5(CARD9):c.1525A>G (p.Arg509Gly)	CARD9 (R509G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1479315	NM_052813.5(CARD9):c.1520C>T (p.Ala507Val)	CARD9 (A507V)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1438789	NM_052813.5(CARD9):c.1517G>A (p.Arg506His)	CARD9 (R506H)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2103411	NM_052813.5(CARD9):c.1512-9T>C	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1629484	NM_052813.5(CARD9):c.1512-18A>G	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1584057	NM_052813.5(CARD9):c.1512-20T>C	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1537403	NM_052813.5(CARD9):c.1511+19G>A	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1977374	NM_052813.5(CARD9):c.1511+17del	CARD9	Deletion (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GBenign
Select item 1125476	NM_052813.5(CARD9):c.1511+7G>A	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 2060413	NM_052813.5(CARD9):c.1511+5G>A	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 961742	NM_052813.5(CARD9):c.1507_1509del (p.Arg504del)	CARD9 (R504del)	Deletion (inframe_deletion +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1921481	NM_052813.5(CARD9):c.1507C>T (p.Arg503Cys)	CARD9 (R503C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1138850	NM_052813.5(CARD9):c.1500G>A (p.Glu500=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 2323573	NM_052813.5(CARD9):c.1492A>G (p.Ser498Gly)	CARD9 (S498G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1006746	NM_052813.5(CARD9):c.1492A>T (p.Ser498Cys)	CARD9 (S498C)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1346662	NM_052813.5(CARD9):c.1489G>A (p.Glu497Lys)	CARD9 (E497K)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 976605	NM_052813.5(CARD9):c.1481G>A (p.Arg494His)	CARD9 (R494H)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 535821	NM_052813.5(CARD9):c.1479G>A (p.Arg493=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 2910565	NM_052813.5(CARD9):c.1474C>A (p.Arg492=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1430391	NM_052813.5(CARD9):c.1465G>A (p.Glu489Lys)	CARD9 (E489K)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1948023	NM_052813.5(CARD9):c.1464C>G (p.Pro488=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1429539	NM_052813.5(CARD9):c.1464C>A (p.Pro488=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 2696659	NM_052813.5(CARD9):c.1461G>A (p.Pro487=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1995636	NM_052813.5(CARD9):c.1456G>C (p.Glu486Gln)	CARD9 (E486Q)	Single nucleotide variant (missense variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 3137347	NM_052813.5(CARD9):c.1454G>C (p.Gly485Ala)	CARD9 (G485A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 535817	NM_052813.5(CARD9):c.1452C>T (p.Ser484=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1556344	NM_052813.5(CARD9):c.1446G>C (p.Leu482=)	CARD9	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +1 more	GLikely benign
Select item 1996310	NM_052813.5(CARD9):c.1441G>C (p.Gly481Arg)	CARD9 (G481R)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1957662	NM_052813.5(CARD9):c.1439C>A (p.Ala480Glu)	CARD9 (A480E)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1955896	NM_052813.5(CARD9):c.1438G>A (p.Ala480Thr)	CARD9 (A480T)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 939222	NM_052813.5(CARD9):c.1437C>A (p.Asp479Glu)	CARD9 (D479E)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2008615	NM_052813.5(CARD9):c.1435G>T (p.Asp479Tyr)	CARD9 (D479Y)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1387145	NM_052813.5(CARD9):c.1435G>A (p.Asp479Asn)	CARD9 (D479N)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2174787	NM_052813.5(CARD9):c.1435-6C>T	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency +1 more	GConflicting classifications of pathogenicity
Select item 2916803	NM_052813.5(CARD9):c.1435-20G>A	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1571734	NM_052813.5(CARD9):c.1435-27_1435-20del	CARD9	Deletion (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1486505	NM_052813.5(CARD9):c.1434+14G>A	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1666752	NM_052813.5(CARD9):c.1434+13C>T	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 3018840	NM_052813.5(CARD9):c.1434+10C>A	CARD9	Single nucleotide variant (intron variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 535816	NM_052813.5(CARD9):c.1434+1G>C	CARD9	Single nucleotide variant (splice donor variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1054703	NM_052813.5(CARD9):c.1434T>C (p.His478=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 661511	NM_052813.5(CARD9):c.1433A>G (p.His478Arg)	CARD9 (H478R)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1381833	NM_052813.5(CARD9):c.1432C>G (p.His478Asp)	CARD9 (H478D)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1366984	NM_052813.5(CARD9):c.1424G>A (p.Arg475Gln)	CARD9 (R475Q)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1021343	NM_052813.5(CARD9):c.1424G>T (p.Arg475Leu)	CARD9 (R475L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1122391	NM_052813.5(CARD9):c.1423C>T (p.Arg475Trp)	CARD9 (R475W)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1036323	NM_052813.5(CARD9):c.1421T>C (p.Leu474Ser)	CARD9 (L474S)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2140376	NM_052813.5(CARD9):c.1410G>A (p.Gln470=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 945012	NM_052813.5(CARD9):c.1407C>A (p.His469Gln)	CARD9 (H469Q)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 858941	NM_052813.5(CARD9):c.1405C>T (p.His469Tyr)	CARD9 (H469Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2810619	NM_052813.5(CARD9):c.1404G>A (p.Leu468=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 2707373	NM_052813.5(CARD9):c.1395T>G (p.Phe465Leu)	CARD9 (F465L)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1607946	NM_052813.5(CARD9):c.1395T>C (p.Phe465=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 365832	NM_052813.5(CARD9):c.1393T>C (p.Phe465Leu)	CARD9 (F465L)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency +1 more	GUncertain significance
Select item 1713423	NM_052813.5(CARD9):c.1391C>G (p.Pro464Arg)	CARD9 (P464R)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1063101	NM_052813.5(CARD9):c.1391C>T (p.Pro464Leu)	CARD9 (P464L)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 2707374	NM_052813.5(CARD9):c.1389G>C (p.Gln463His)	CARD9 (Q463H)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1139400	NM_052813.5(CARD9):c.1389G>A (p.Gln463=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 365833	NM_052813.5(CARD9):c.1383G>A (p.Pro461=)	CARD9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 365834	NM_052813.5(CARD9):c.1382C>T (p.Pro461Leu)	CARD9 (P461L)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 1159643	NM_052813.5(CARD9):c.1377G>A (p.Gly459=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 1148642	NM_052813.5(CARD9):c.1374G>C (p.Gly458=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 3137346	NM_052813.5(CARD9):c.1373G>T (p.Gly458Val)	CARD9 (G458V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 735201	NM_052813.5(CARD9):c.1373G>C (p.Gly458Ala)	CARD9 (G458A)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign
Select item 849328	NM_052813.5(CARD9):c.1369G>A (p.Gly457Ser)	CARD9 (G457S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1021548	NM_052813.5(CARD9):c.1361G>A (p.Cys454Tyr)	CARD9 (C454Y)	Single nucleotide variant (missense variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GUncertain significance
Select item 535822	NM_052813.5(CARD9):c.1359C>A (p.Gly453=)	CARD9	Single nucleotide variant (synonymous variant)	Predisposition to invasive fungal disease due to CARD9 deficiency	GLikely benign

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