List of variants in gene PKHD1 reported as uncertain significance by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_138694.4(PKHD1):c.9925A>G (p.Ile3309Val)	rs45627337	0.00036
NM_138694.4(PKHD1):c.12142C>T (p.Gln4048Ter)	rs201812542	0.00022
NM_138694.4(PKHD1):c.4009G>A (p.Asp1337Asn)	rs373255125	0.00008
NM_138694.4(PKHD1):c.11881C>T (p.Arg3961Ter)	rs144193508	0.00001
NM_138694.4(PKHD1):c.12225A>T (p.Ter4075Cys)	rs1347911533	0.00001
NM_138694.4(PKHD1):c.2167C>T (p.Arg723Cys)	rs794727366	0.00001
NM_138694.4(PKHD1):c.10075G>C (p.Gly3359Arg)
NM_138694.4(PKHD1):c.1166C>T (p.Thr389Ile)
NM_138694.4(PKHD1):c.166T>C (p.Ser56Pro)
NM_138694.4(PKHD1):c.2179A>G (p.Asn727Asp)
NM_138694.4(PKHD1):c.2948G>A (p.Cys983Tyr)	rs1554208064
NM_138694.4(PKHD1):c.3373A>G (p.Thr1125Ala)	rs144365187
NM_138694.4(PKHD1):c.5358C>G (p.Ser1786Arg)
NM_138694.4(PKHD1):c.619G>T (p.Asp207Tyr)
NM_138694.4(PKHD1):c.6332+2T>A	rs1783090781
NM_138694.4(PKHD1):c.712A>G (p.Met238Val)
NM_138694.4(PKHD1):c.9705T>A (p.Asn3235Lys)	rs759568939

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.