ClinVar Miner

List of variants reported as uncertain significance for Bifunctional peroxisomal enzyme deficiency by Counsyl

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000414.4(HSD17B4):c.743G>A (p.Arg248His) rs748057401 0.00003
NM_000414.4(HSD17B4):c.2116C>T (p.Gln706Ter) rs771510541 0.00001
NM_000414.4(HSD17B4):c.2122-2A>G rs1341761252 0.00001
NM_000414.4(HSD17B4):c.58+121A>G rs775377217 0.00001
NM_000414.4(HSD17B4):c.58+123G>C rs762157656 0.00001
NM_000414.4(HSD17B4):c.1517G>A (p.Arg506His) rs1554068136
NM_000414.4(HSD17B4):c.1538C>T (p.Pro513Leu) rs587777444
NM_000414.4(HSD17B4):c.1574G>T (p.Gly525Val) rs1554068261
NM_000414.4(HSD17B4):c.1586C>T (p.Pro529Leu) rs1554068269
NM_000414.4(HSD17B4):c.1595A>G (p.His532Arg) rs1554068272
NM_000414.4(HSD17B4):c.178GAA[1] (p.Glu61del) rs1554062119
NM_000414.4(HSD17B4):c.2130dup (p.Ser711Ter) rs1554070146
NM_000414.4(HSD17B4):c.216C>A (p.Asn72Lys) rs1554062124
NM_000414.4(HSD17B4):c.298G>T (p.Ala100Ser) rs1554062352
NM_000414.4(HSD17B4):c.523G>A (p.Ala175Thr) rs1554062814
NM_000414.4(HSD17B4):c.58+189del rs1554059560
NM_000414.4(HSD17B4):c.661C>T (p.Leu221Phe) rs1554064092
NM_000414.4(HSD17B4):c.739+2dup rs1554064396

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.