ClinVar Miner

List of variants in gene ZDHHC9 reported as uncertain significance for developmental disorder of mental health

Included ClinVar conditions (728):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_016032.4(ZDHHC9):c.881+3G>A rs775743190 0.00004
NM_016032.4(ZDHHC9):c.929G>A (p.Arg310Gln) rs753387074 0.00003
NM_016032.4(ZDHHC9):c.1001C>T (p.Ser334Leu) rs748573163 0.00002
NM_016032.4(ZDHHC9):c.160G>A (p.Ala54Thr) rs1003990057 0.00002
NM_016032.4(ZDHHC9):c.331G>T (p.Ala111Ser) rs753548428 0.00002
NM_016032.4(ZDHHC9):c.344C>T (p.Ala115Val) rs1413588337 0.00002
NM_016032.4(ZDHHC9):c.1013C>T (p.Pro338Leu) rs753807510 0.00001
NM_016032.4(ZDHHC9):c.1025G>A (p.Ser342Asn) rs1242322529 0.00001
NM_016032.4(ZDHHC9):c.1045C>T (p.Pro349Ser) rs755700206 0.00001
NM_016032.4(ZDHHC9):c.1054C>A (p.Pro352Thr) rs745341099 0.00001
NM_016032.4(ZDHHC9):c.20G>C (p.Arg7Thr) rs1488428088 0.00001
NM_016032.4(ZDHHC9):c.329-2dup rs763845850 0.00001
NM_016032.4(ZDHHC9):c.362G>A (p.Arg121Gln) rs1159950184 0.00001
NM_016032.4(ZDHHC9):c.778A>G (p.Ile260Val) rs1927640133 0.00001
NM_016032.4(ZDHHC9):c.893G>A (p.Arg298Gln) rs869312679 0.00001
NM_016032.4(ZDHHC9):c.989A>G (p.Glu330Gly) rs1370221742 0.00001
NM_016032.4(ZDHHC9):c.98G>A (p.Arg33Gln) rs767597857 0.00001
NM_016032.4(ZDHHC9):c.1003A>T (p.Asn335Tyr)
NM_016032.4(ZDHHC9):c.1021A>G (p.Ser341Gly)
NM_016032.4(ZDHHC9):c.1028C>T (p.Thr343Ile) rs2124096171
NM_016032.4(ZDHHC9):c.1034A>C (p.Glu345Ala)
NM_016032.4(ZDHHC9):c.1055C>G (p.Pro352Arg) rs893901934
NM_016032.4(ZDHHC9):c.1075G>A (p.Ala359Thr) rs1927515432
NM_016032.4(ZDHHC9):c.1084G>C (p.Ala362Pro)
NM_016032.4(ZDHHC9):c.180G>A (p.Leu60=)
NM_016032.4(ZDHHC9):c.184G>A (p.Val62Ile)
NM_016032.4(ZDHHC9):c.197C>T (p.Pro66Leu)
NM_016032.4(ZDHHC9):c.220A>G (p.Met74Val)
NM_016032.4(ZDHHC9):c.222G>A (p.Met74Ile)
NM_016032.4(ZDHHC9):c.23A>G (p.Lys8Arg)
NM_016032.4(ZDHHC9):c.244A>G (p.Thr82Ala) rs2124124631
NM_016032.4(ZDHHC9):c.266G>C (p.Ser89Thr)
NM_016032.4(ZDHHC9):c.274G>A (p.Gly92Arg) rs2124124576
NM_016032.4(ZDHHC9):c.313A>G (p.Ile105Val) rs2124124514
NM_016032.4(ZDHHC9):c.328G>A (p.Glu110Lys)
NM_016032.4(ZDHHC9):c.373C>T (p.Arg125Cys)
NM_016032.4(ZDHHC9):c.397A>C (p.Asn133His) rs1556006445
NM_016032.4(ZDHHC9):c.399C>A (p.Asn133Lys) rs911311531
NM_016032.4(ZDHHC9):c.412C>A (p.Leu138Met) rs142944444
NM_016032.4(ZDHHC9):c.421T>C (p.Cys141Arg) rs1927945327
NM_016032.4(ZDHHC9):c.443G>A (p.Arg148Gln) rs2124117199
NM_016032.4(ZDHHC9):c.491G>A (p.Arg164His)
NM_016032.4(ZDHHC9):c.496G>A (p.Asp166Asn) rs2124105757
NM_016032.4(ZDHHC9):c.516G>A (p.Val172=)
NM_016032.4(ZDHHC9):c.523T>G (p.Cys175Gly) rs2124105731
NM_016032.4(ZDHHC9):c.53C>G (p.Pro18Arg) rs1928391209
NM_016032.4(ZDHHC9):c.544C>T (p.Arg182Cys) rs2124105703
NM_016032.4(ZDHHC9):c.562A>G (p.Ile188Val)
NM_016032.4(ZDHHC9):c.566T>C (p.Leu189Pro)
NM_016032.4(ZDHHC9):c.586A>G (p.Ile196Val)
NM_016032.4(ZDHHC9):c.601T>C (p.Phe201Leu) rs2124105600
NM_016032.4(ZDHHC9):c.614A>G (p.Tyr205Cys) rs2124105555
NM_016032.4(ZDHHC9):c.673A>G (p.Thr225Ala) rs1927697408
NM_016032.4(ZDHHC9):c.698T>C (p.Phe233Ser)
NM_016032.4(ZDHHC9):c.715G>A (p.Val239Ile)
NM_016032.4(ZDHHC9):c.718G>A (p.Val240Met)
NM_016032.4(ZDHHC9):c.718G>C (p.Val240Leu) rs770589013
NM_016032.4(ZDHHC9):c.764C>A (p.Thr255Lys) rs1927670769
NM_016032.4(ZDHHC9):c.76G>A (p.Asp26Asn)
NM_016032.4(ZDHHC9):c.770A>G (p.Asn257Ser)
NM_016032.4(ZDHHC9):c.790T>C (p.Trp264Arg)
NM_016032.4(ZDHHC9):c.805C>T (p.Arg269Cys)
NM_016032.4(ZDHHC9):c.913G>C (p.Glu305Gln)
NM_016032.4(ZDHHC9):c.925A>G (p.Ser309Gly) rs1927626006
NM_016032.4(ZDHHC9):c.949A>T (p.Thr317Ser) rs1927624839
NM_016032.4(ZDHHC9):c.952A>T (p.Ser318Cys)
NM_016032.4(ZDHHC9):c.961C>T (p.Leu321Phe)
NM_016032.4(ZDHHC9):c.978+6T>G
NM_016032.4(ZDHHC9):c.979G>A (p.Ala327Thr)
NM_016032.4(ZDHHC9):c.984del (p.Thr329fs) rs779289842

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