"Fulgent Genetics, Fulgent Genetics"[submitter] AND "ZDHHC24"[gene] - ClinVar

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Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 552356	NM_024649.5(BBS1):c.724-1G>C	BBS1, ZDHHC24	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome +1 more	GPathogenic/Likely pathogenic
Select item 969824	NM_024649.5(BBS1):c.725T>C (p.Met242Thr)	BBS1, ZDHHC24 (M242T)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome +2 more	GUncertain significance
Select item 283883	NM_024649.5(BBS1):c.726G>A (p.Met242Ile)	BBS1, ZDHHC24 (M242I)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome 1 +2 more	GUncertain significance
Select item 970728	NM_024649.5(BBS1):c.734C>T (p.Pro245Leu)	BBS1, ZDHHC24 (P245L)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome +2 more	GUncertain significance
Select item 863198	NM_024649.5(BBS1):c.739G>A (p.Val247Ile)	ZDHHC24, BBS1 (V247I)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 990065	NM_024649.5(BBS1):c.742C>A (p.Pro248Thr)	BBS1, ZDHHC24 (P248T)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome 1	GUncertain significance
Select item 966229	NM_024649.5(BBS1):c.751C>G (p.Leu251Val)	BBS1, ZDHHC24 (L251V)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 289320	NM_024649.5(BBS1):c.772G>C (p.Asp258His)	BBS1, ZDHHC24 (D258H)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome 1 +3 more	GUncertain significance
Select item 1336076	NM_024649.5(BBS1):c.802C>T (p.Arg268Cys)	ZDHHC24, BBS1 (R268C)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome 1 +2 more	GUncertain significance
Select item 1490603	NM_024649.5(BBS1):c.808G>A (p.Gly270Arg)	BBS1, ZDHHC24 (G270R)	Single nucleotide variant (3 prime UTR variant +1 more)	Bardet-Biedl syndrome 1 +2 more	GUncertain significance
Select item 1578915	NM_024649.5(BBS1):c.830+12del	BBS1, ZDHHC24	Deletion (3 prime UTR variant +1 more)	Bardet-Biedl syndrome +1 more	GLikely benign
Select item 371274	NM_024649.5(BBS1):c.871C>T (p.Gln291Ter)	BBS1, ZDHHC24 (Q291*)	Single nucleotide variant (nonsense +1 more)	Bardet-Biedl syndrome 1 +2 more	GPathogenic
Select item 305463	NM_024649.5(BBS1):c.877G>A (p.Val293Met)	BBS1, ZDHHC24 (V293M)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +3 more	GUncertain significance
Select item 574647	NM_024649.5(BBS1):c.887T>C (p.Ile296Thr)	BBS1, ZDHHC24 (I296T)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +3 more	GUncertain significance
Select item 193740	NM_024649.5(BBS1):c.887del (p.Ile296fs)	BBS1, ZDHHC24 (I296fs)	Deletion (frameshift variant +1 more)	Retinal dystrophy +3 more	GPathogenic
Select item 842189	NM_024649.5(BBS1):c.901G>A (p.Val301Ile)	BBS1, ZDHHC24 (V301I)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 1051033	NM_024649.5(BBS1):c.910G>T (p.Val304Leu)	ZDHHC24, BBS1 (V304L)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 917920	NM_024649.5(BBS1):c.951+58C>T	BBS1, ZDHHC24	Single nucleotide variant (intron variant)	Bardet-Biedl syndrome +2 more	GPathogenic
Select item 695359	NM_024649.5(BBS1):c.1020C>G (p.Ser340=)	BBS1, ZDHHC24	Single nucleotide variant (synonymous variant +1 more)	Bardet-Biedl syndrome 1 +2 more	GBenign/Likely benign
Select item 944920	NM_024649.5(BBS1):c.1021C>T (p.Arg341Trp)	BBS1, ZDHHC24 (R341W)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 1026513	NM_024649.5(BBS1):c.1054A>G (p.Asn352Asp)	BBS1, ZDHHC24 (N352D)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +1 more	GUncertain significance
Select item 462951	NM_024649.5(BBS1):c.1088T>C (p.Leu363Pro)	BBS1, ZDHHC24 (L363P)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +2 more	GUncertain significance
Select item 843339	NM_024649.5(BBS1):c.1109C>T (p.Pro370Leu)	BBS1, ZDHHC24 (P370L)	Single nucleotide variant (missense variant +1 more)	BBS1-related condition +2 more	GUncertain significance
Select item 834889	NM_024649.5(BBS1):c.1111-2A>G	BBS1, ZDHHC24	Single nucleotide variant (splice acceptor variant +1 more)	Bardet-Biedl syndrome +1 more	GLikely pathogenic
Select item 216740	NM_024649.5(BBS1):c.1139G>A (p.Arg380Gln)	BBS1, ZDHHC24 (R380Q)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +3 more	GUncertain significance
Select item 806695	NM_024649.5(BBS1):c.1144G>A (p.Gly382Arg)	BBS1, ZDHHC24 (G382R)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +2 more	GUncertain significance
Select item 12143	NM_024649.5(BBS1):c.1169T>G (p.Met390Arg)	BBS1, ZDHHC24 (M390R)	Single nucleotide variant (missense variant +1 more)	Retinal dystrophy +6 more	GPathogenic/Likely pathogenic
Select item 1434361	NM_024649.5(BBS1):c.1175C>A (p.Thr392Asn)	BBS1, ZDHHC24 (T392N)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +2 more	GUncertain significance
Select item 840928	NM_024649.5(BBS1):c.1243G>A (p.Val415Met)	BBS1, ZDHHC24 (V415M)	Single nucleotide variant (missense variant +1 more)	BBS1-related condition +3 more	GUncertain significance
Select item 462952	NM_024649.5(BBS1):c.1277A>G (p.Asn426Ser)	BBS1, ZDHHC24 (N426S)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +3 more	GConflicting classifications of pathogenicity
Select item 188983	NM_024649.5(BBS1):c.1285C>T (p.Arg429Ter)	BBS1, ZDHHC24 (R429*)	Single nucleotide variant (nonsense +1 more)	Bardet-Biedl syndrome +2 more	GPathogenic/Likely pathogenic
Select item 1440266	NM_024649.5(BBS1):c.1294C>T (p.Arg432Trp)	BBS1, ZDHHC24 (R432W)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 840005	NM_024649.5(BBS1):c.1310A>T (p.Gln437Leu)	BBS1, ZDHHC24 (Q437L)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +1 more	GUncertain significance
Select item 531824	NM_024649.5(BBS1):c.1339G>A (p.Ala447Thr)	BBS1, ZDHHC24 (A447T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +3 more	GPathogenic/Likely pathogenic
Select item 305470	NM_024649.5(BBS1):c.1394G>A (p.Arg465His)	BBS1, ZDHHC24 (R465H)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 531828	NM_024649.5(BBS1):c.1439C>A (p.Thr480Lys)	BBS1, ZDHHC24 (T480K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 649714	NM_024649.5(BBS1):c.1447C>T (p.Arg483Ter)	BBS1, ZDHHC24 (R483*)	Single nucleotide variant (nonsense +1 more)	not provided +3 more	GPathogenic
Select item 1444932	NM_024649.5(BBS1):c.1448G>A (p.Arg483Gln)	BBS1, ZDHHC24 (R483Q)	Single nucleotide variant (missense variant +1 more)	Retinal dystrophy +2 more	GUncertain significance
Select item 1136978	NM_024649.5(BBS1):c.1470C>T (p.Ala490=)	BBS1, ZDHHC24	Single nucleotide variant (synonymous variant +1 more)	Bardet-Biedl syndrome 1 +2 more	GLikely benign
Select item 1419919	NM_024649.5(BBS1):c.1471G>A (p.Val491Met)	BBS1, ZDHHC24 (V491M)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +1 more	GUncertain significance
Select item 1121939	NM_024649.5(BBS1):c.1474-14C>T	BBS1, ZDHHC24	Single nucleotide variant (intron variant)	Bardet-Biedl syndrome +1 more	GLikely benign
Select item 1450459	NM_024649.5(BBS1):c.1474G>T (p.Val492Phe)	BBS1, ZDHHC24 (V492F)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +2 more	GUncertain significance
Select item 700439	NM_024649.5(BBS1):c.1485T>C (p.Leu495=)	BBS1, ZDHHC24	Single nucleotide variant (synonymous variant +1 more)	BBS1-related condition +2 more	GLikely benign
Select item 990494	NM_024649.5(BBS1):c.1489C>A (p.Pro497Thr)	BBS1, ZDHHC24 (P497T)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1	GUncertain significance
Select item 990495	NM_024649.5(BBS1):c.1528A>G (p.Thr510Ala)	BBS1, ZDHHC24 (T510A)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1	GUncertain significance
Select item 969583	NM_024649.5(BBS1):c.1534C>A (p.Arg512Ser)	BBS1, ZDHHC24 (R512S)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 1103931	NM_024649.5(BBS1):c.1554G>T (p.Leu518=)	ZDHHC24, BBS1	Single nucleotide variant (synonymous variant +1 more)	Bardet-Biedl syndrome +1 more	GLikely benign
Select item 879584	NM_024649.5(BBS1):c.1592C>T (p.Pro531Leu)	BBS1, ZDHHC24 (P531L)	Single nucleotide variant (missense variant +1 more)	BBS1-related condition +3 more	GUncertain significance
Select item 393063	NM_024649.5(BBS1):c.1594C>T (p.Arg532Trp)	BBS1, ZDHHC24 (R532W)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +3 more	GUncertain significance
Select item 862497	NM_024649.5(BBS1):c.1595G>T (p.Arg532Leu)	BBS1, ZDHHC24 (R532L)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +1 more	GUncertain significance
Select item 285977	NM_024649.5(BBS1):c.1595G>A (p.Arg532Gln)	BBS1, ZDHHC24 (R532Q)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 813017	NM_024649.5(BBS1):c.1608+1G>A	BBS1, ZDHHC24	Single nucleotide variant (splice donor variant +1 more)	Bardet-Biedl syndrome 1 +1 more	GPathogenic/Likely pathogenic
Select item 12144	NM_024649.5(BBS1):c.1645G>T (p.Glu549Ter)	BBS1, ZDHHC24 (E549*)	Single nucleotide variant (nonsense +1 more)	Inborn genetic diseases +5 more	GPathogenic/Likely pathogenic
Select item 636150	NM_024649.5(BBS1):c.1660A>T (p.Ser554Cys)	BBS1, ZDHHC24 (S554C)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +2 more	GUncertain significance
Select item 305473	NM_024649.5(BBS1):c.1744G>A (p.Val582Ile)	BBS1, ZDHHC24 (V582I)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +2 more	GUncertain significance
Select item 1379366	NM_024649.5(BBS1):c.1752G>A (p.Met584Ile)	BBS1, ZDHHC24 (M584I)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +1 more	GUncertain significance
Select item 391252	NM_024649.5(BBS1):c.1772C>T (p.Ala591Val)	ZDHHC24, BBS1 (A591V)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome +3 more	GUncertain significance
Select item 697719	NM_024649.5(BBS1):c.1773G>A (p.Ala591=)	BBS1, ZDHHC24	Single nucleotide variant (synonymous variant +1 more)	BBS1-related condition +2 more	GLikely benign
Select item 1110464	NM_024649.5(BBS1):c.1776C>T (p.Ala592=)	BBS1, ZDHHC24	Single nucleotide variant (synonymous variant +1 more)	BBS1-related condition +2 more	GLikely benign
Select item 1417809	NM_024649.5(BBS1):c.1777G>A (p.Ala593Thr)	BBS1, ZDHHC24 (A593T)	Single nucleotide variant (missense variant +1 more)	Bardet-Biedl syndrome 1 +1 more	GUncertain significance

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Items: 60