ClinVar Miner

List of variants in gene ZDHHC9 reported as likely benign for X-linked syndromic intellectual disability

Included ClinVar conditions (104):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_016032.4(ZDHHC9):c.328+17G>T rs368495079 0.00014
NM_016032.4(ZDHHC9):c.384T>C (p.Asn128=) rs141113457 0.00004
NM_016032.4(ZDHHC9):c.324G>A (p.Glu108=) rs372929200 0.00003
NM_016032.4(ZDHHC9):c.488-17C>T rs367846813 0.00003
NM_016032.4(ZDHHC9):c.1056C>T (p.Pro352=) rs1381138968 0.00002
NM_016032.4(ZDHHC9):c.598G>A (p.Ala200Thr) rs769527426 0.00002
NM_016032.4(ZDHHC9):c.861G>T (p.Leu287=) rs761777228 0.00002
NM_016032.4(ZDHHC9):c.136C>T (p.Leu46=) rs768836456 0.00001
NM_016032.4(ZDHHC9):c.357C>A (p.Gly119=) rs751652102 0.00001
NM_016032.4(ZDHHC9):c.414G>T (p.Leu138=) rs1240954820 0.00001
NM_016032.4(ZDHHC9):c.429A>G (p.Thr143=) rs377127210 0.00001
NM_016032.4(ZDHHC9):c.489G>A (p.Glu163=) rs1339214564 0.00001
NM_016032.4(ZDHHC9):c.519G>A (p.Gly173=) rs766780497 0.00001
NM_016032.4(ZDHHC9):c.549C>T (p.Tyr183=) rs773907113 0.00001
NM_016032.4(ZDHHC9):c.561C>T (p.Phe187=) rs1328392655 0.00001
NM_016032.4(ZDHHC9):c.579C>T (p.Leu193=) rs748827100 0.00001
NM_016032.4(ZDHHC9):c.666T>A (p.Thr222=) rs1199031410 0.00001
NM_016032.4(ZDHHC9):c.777C>T (p.Asp259=) rs751918374 0.00001
NM_016032.4(ZDHHC9):c.789A>G (p.Ser263=) rs763972982 0.00001
NM_016032.4(ZDHHC9):c.808G>A (p.Val270Ile) rs773050995 0.00001
NM_016032.4(ZDHHC9):c.85G>A (p.Val29Ile) rs773173211 0.00001
NM_016032.4(ZDHHC9):c.881+8G>C rs1295858000 0.00001
NM_016032.4(ZDHHC9):c.888G>A (p.Leu296=) rs944227274 0.00001
NM_016032.4(ZDHHC9):c.936C>T (p.Pro312=) rs371820381 0.00001
NM_016032.4(ZDHHC9):c.954T>C (p.Ser318=) rs1458539537 0.00001
NM_016032.4(ZDHHC9):c.979-6T>C rs374438182 0.00001
NM_016032.4(ZDHHC9):c.981C>T (p.Ala327=) rs1429612573 0.00001
NM_016032.4(ZDHHC9):c.9G>A (p.Val3=) rs752507178 0.00001
NM_016032.4(ZDHHC9):c.1030C>T (p.Pro344Ser)
NM_016032.4(ZDHHC9):c.1032C>G (p.Pro344=)
NM_016032.4(ZDHHC9):c.1038G>A (p.Glu346=)
NM_016032.4(ZDHHC9):c.1064_1065insCCCACAGCC (p.Pro355_Gln357dup) rs1413822794
NM_016032.4(ZDHHC9):c.120G>T (p.Leu40=)
NM_016032.4(ZDHHC9):c.141G>A (p.Gly47=) rs1602966301
NM_016032.4(ZDHHC9):c.144A>G (p.Thr48=) rs145877196
NM_016032.4(ZDHHC9):c.153C>T (p.Leu51=)
NM_016032.4(ZDHHC9):c.159C>T (p.Phe53=) rs2124141125
NM_016032.4(ZDHHC9):c.328+11C>T rs769825368
NM_016032.4(ZDHHC9):c.328+16del rs2124124472
NM_016032.4(ZDHHC9):c.329-11T>C
NM_016032.4(ZDHHC9):c.332C>T (p.Ala111Val) rs1556006489
NM_016032.4(ZDHHC9):c.336C>T (p.Thr112=)
NM_016032.4(ZDHHC9):c.345G>A (p.Ala115=)
NM_016032.4(ZDHHC9):c.36G>A (p.Arg12=)
NM_016032.4(ZDHHC9):c.36G>C (p.Arg12=) rs1602966376
NM_016032.4(ZDHHC9):c.396C>T (p.Asn132=)
NM_016032.4(ZDHHC9):c.411A>G (p.Lys137=)
NM_016032.4(ZDHHC9):c.487+14_487+15inv
NM_016032.4(ZDHHC9):c.487+19A>G
NM_016032.4(ZDHHC9):c.487+19A>T
NM_016032.4(ZDHHC9):c.487+20C>T
NM_016032.4(ZDHHC9):c.487+8A>G rs960379555
NM_016032.4(ZDHHC9):c.488-15C>T rs759659851
NM_016032.4(ZDHHC9):c.488-17C>G
NM_016032.4(ZDHHC9):c.488-19C>T
NM_016032.4(ZDHHC9):c.488-5del rs2124105781
NM_016032.4(ZDHHC9):c.488-9C>A rs113127450
NM_016032.4(ZDHHC9):c.495C>T (p.Phe165=)
NM_016032.4(ZDHHC9):c.51C>T (p.Leu17=) rs2124141410
NM_016032.4(ZDHHC9):c.531A>G (p.Gly177=)
NM_016032.4(ZDHHC9):c.597C>T (p.Phe199=)
NM_016032.4(ZDHHC9):c.612C>T (p.Val204=)
NM_016032.4(ZDHHC9):c.625+10C>T
NM_016032.4(ZDHHC9):c.625+14G>A
NM_016032.4(ZDHHC9):c.626-11C>T rs2124104577
NM_016032.4(ZDHHC9):c.626-16C>T
NM_016032.4(ZDHHC9):c.674+7T>C rs1927697269
NM_016032.4(ZDHHC9):c.718G>C (p.Val240Leu) rs770589013
NM_016032.4(ZDHHC9):c.747C>T (p.Leu249=)
NM_016032.4(ZDHHC9):c.778-11T>G
NM_016032.4(ZDHHC9):c.778-15G>T
NM_016032.4(ZDHHC9):c.778-4G>C
NM_016032.4(ZDHHC9):c.795A>T (p.Thr265=) rs2124101786
NM_016032.4(ZDHHC9):c.807C>A (p.Arg269=)
NM_016032.4(ZDHHC9):c.807C>T (p.Arg269=)
NM_016032.4(ZDHHC9):c.858G>T (p.Val286=) rs1556004572
NM_016032.4(ZDHHC9):c.873G>A (p.Leu291=) rs1556004565
NM_016032.4(ZDHHC9):c.876C>T (p.Pro292=) rs1556004557
NM_016032.4(ZDHHC9):c.881+10G>C rs2124101663
NM_016032.4(ZDHHC9):c.881+17A>G
NM_016032.4(ZDHHC9):c.882-19dup
NM_016032.4(ZDHHC9):c.900T>C (p.Gly300=) rs1556004503
NM_016032.4(ZDHHC9):c.956G>A (p.Ser319Asn)
NM_016032.4(ZDHHC9):c.978+7G>A

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