ClinVar Miner

List of variants in gene HDAC8 reported as likely benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_018486.3(HDAC8):c.384C>T (p.Asp128=) rs1250641302 0.00008
NM_018486.3(HDAC8):c.213C>T (p.His71=) rs782349794 0.00006
NM_018486.3(HDAC8):c.629-14C>T rs1164078285 0.00005
NM_018486.3(HDAC8):c.834C>T (p.Asn278=) rs781878660 0.00004
NM_018486.3(HDAC8):c.915C>G (p.Gly305=) rs782121649 0.00003
NM_018486.3(HDAC8):c.281T>C (p.Ile94Thr) rs1452290404 0.00002
NM_018486.3(HDAC8):c.318A>G (p.Glu106=) rs1388554395 0.00002
NM_018486.3(HDAC8):c.429T>C (p.His143=) rs374885534 0.00002
NM_018486.3(HDAC8):c.561C>T (p.Asp187=) rs931276707 0.00002
NM_018486.3(HDAC8):c.756C>T (p.Tyr252=) rs368682006 0.00002
NM_018486.3(HDAC8):c.1052G>C (p.Ser351Thr) rs782558250 0.00001
NM_018486.3(HDAC8):c.135T>C (p.Ile45=) rs1556159779 0.00001
NM_018486.3(HDAC8):c.342T>C (p.Ala114=) rs1324464792 0.00001
NM_018486.3(HDAC8):c.1053C>T (p.Ser351=)
NM_018486.3(HDAC8):c.1058G>A (p.Arg353Gln)
NM_018486.3(HDAC8):c.1066C>T (p.Arg356Cys)
NM_018486.3(HDAC8):c.1068C>A (p.Arg356=)
NM_018486.3(HDAC8):c.1104C>T (p.Tyr368=)
NM_018486.3(HDAC8):c.1105A>G (p.Ile369Val)
NM_018486.3(HDAC8):c.111+10G>A
NM_018486.3(HDAC8):c.111+14G>C rs2147618204
NM_018486.3(HDAC8):c.111+20A>G
NM_018486.3(HDAC8):c.111+7G>A rs2147618283
NM_018486.3(HDAC8):c.1111+13C>T
NM_018486.3(HDAC8):c.1111+17del
NM_018486.3(HDAC8):c.1112-10_1112-9del
NM_018486.3(HDAC8):c.1112-11C>G
NM_018486.3(HDAC8):c.1112-5T>G
NM_018486.3(HDAC8):c.112-11G>T
NM_018486.3(HDAC8):c.112-14G>A
NM_018486.3(HDAC8):c.141A>T (p.Ala47=)
NM_018486.3(HDAC8):c.164+9T>C
NM_018486.3(HDAC8):c.165-11G>A
NM_018486.3(HDAC8):c.21G>C (p.Pro7=) rs1603246257
NM_018486.3(HDAC8):c.225T>C (p.Tyr75=)
NM_018486.3(HDAC8):c.296-13T>C
NM_018486.3(HDAC8):c.296-6C>T
NM_018486.3(HDAC8):c.306C>T (p.Cys102=)
NM_018486.3(HDAC8):c.330C>T (p.Asp110=) rs2051865907
NM_018486.3(HDAC8):c.381T>A (p.Ile127=)
NM_018486.3(HDAC8):c.437+13C>G
NM_018486.3(HDAC8):c.437+16_437+19del
NM_018486.3(HDAC8):c.477C>T (p.Val159=)
NM_018486.3(HDAC8):c.487T>C (p.Leu163=)
NM_018486.3(HDAC8):c.491G>T (p.Arg164Leu)
NM_018486.3(HDAC8):c.499C>T (p.Arg167Trp)
NM_018486.3(HDAC8):c.510G>A (p.Glu170=)
NM_018486.3(HDAC8):c.525G>A (p.Val175=)
NM_018486.3(HDAC8):c.550+7C>T
NM_018486.3(HDAC8):c.550+9T>G
NM_018486.3(HDAC8):c.551-17G>A
NM_018486.3(HDAC8):c.558A>G (p.Glu186=) rs2148131646
NM_018486.3(HDAC8):c.603C>T (p.His201=)
NM_018486.3(HDAC8):c.615A>G (p.Pro205=)
NM_018486.3(HDAC8):c.628+20G>A rs2148131378
NM_018486.3(HDAC8):c.628+7G>A
NM_018486.3(HDAC8):c.629-11C>G
NM_018486.3(HDAC8):c.629-16C>T
NM_018486.3(HDAC8):c.629-18T>C
NM_018486.3(HDAC8):c.657A>C (p.Leu219=)
NM_018486.3(HDAC8):c.666A>G (p.Gly222=)
NM_018486.3(HDAC8):c.66C>G (p.Pro22=)
NM_018486.3(HDAC8):c.66C>T (p.Pro22=)
NM_018486.3(HDAC8):c.737+16_737+28del
NM_018486.3(HDAC8):c.738-17del
NM_018486.3(HDAC8):c.738-4A>G rs782294776
NM_018486.3(HDAC8):c.747G>A (p.Lys249=)
NM_018486.3(HDAC8):c.767A>T (p.Asn256Ile)
NM_018486.3(HDAC8):c.828C>T (p.Ser276=)
NM_018486.3(HDAC8):c.894A>G (p.Thr298=)
NM_018486.3(HDAC8):c.910+20A>G rs2148045760
NM_018486.3(HDAC8):c.911-13T>C
NM_018486.3(HDAC8):c.927C>T (p.Ala309=)
NM_018486.3(HDAC8):c.930C>T (p.Asn310=)
NM_018486.3(HDAC8):c.951C>T (p.Tyr317=) rs1555991936
NM_018486.3(HDAC8):c.957C>T (p.Thr319=) rs782144834

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