ClinVar Miner

List of variants reported as uncertain significance for Primary hyperoxaluria, type III by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 55
Download table as spreadsheet
HGVS dbSNP
NM_138413.4(HOGA1):c.*101C>T rs41290458
NM_138413.4(HOGA1):c.*1047T>C rs537101942
NM_138413.4(HOGA1):c.*1059A>C rs886047524
NM_138413.4(HOGA1):c.*109C>T
NM_138413.4(HOGA1):c.*186C>A rs576078709
NM_138413.4(HOGA1):c.*186C>T rs576078709
NM_138413.4(HOGA1):c.*288A>C rs886047520
NM_138413.4(HOGA1):c.*289C>T rs540860054
NM_138413.4(HOGA1):c.*290G>A rs144890621
NM_138413.4(HOGA1):c.*291C>T
NM_138413.4(HOGA1):c.*292C>T rs771988623
NM_138413.4(HOGA1):c.*352T>C rs545072905
NM_138413.4(HOGA1):c.*360C>T
NM_138413.4(HOGA1):c.*391T>C
NM_138413.4(HOGA1):c.*425T>C rs189957405
NM_138413.4(HOGA1):c.*427G>A
NM_138413.4(HOGA1):c.*485C>T rs553100036
NM_138413.4(HOGA1):c.*550A>G
NM_138413.4(HOGA1):c.*55T>C
NM_138413.4(HOGA1):c.*592C>G
NM_138413.4(HOGA1):c.*592C>T
NM_138413.4(HOGA1):c.*593G>A
NM_138413.4(HOGA1):c.*665C>T
NM_138413.4(HOGA1):c.*68C>T
NM_138413.4(HOGA1):c.*733C>T rs764120248
NM_138413.4(HOGA1):c.*803A>G
NM_138413.4(HOGA1):c.*850G>T rs560555907
NM_138413.4(HOGA1):c.*887C>G
NM_138413.4(HOGA1):c.*937C>T
NM_138413.4(HOGA1):c.*950G>A rs190392004
NM_138413.4(HOGA1):c.-224G>A
NM_138413.4(HOGA1):c.134C>G (p.Pro45Arg)
NM_138413.4(HOGA1):c.153G>T (p.Glu51Asp)
NM_138413.4(HOGA1):c.185A>T (p.His62Leu) rs150812556
NM_138413.4(HOGA1):c.208C>T (p.Arg70Ter) rs758304537
NM_138413.4(HOGA1):c.212-6T>C rs372066473
NM_138413.4(HOGA1):c.237C>T (p.Gly79=) rs148094180
NM_138413.4(HOGA1):c.269T>A (p.Leu90His)
NM_138413.4(HOGA1):c.39G>A (p.Gly13=) rs200127255
NM_138413.4(HOGA1):c.424C>T (p.Arg142Cys)
NM_138413.4(HOGA1):c.448C>T (p.Leu150Phe)
NM_138413.4(HOGA1):c.538G>A (p.Val180Met) rs114177505
NM_138413.4(HOGA1):c.554C>T (p.Thr185Met) rs115282699
NM_138413.4(HOGA1):c.604-4G>T
NM_138413.4(HOGA1):c.661G>A (p.Ala221Thr)
NM_138413.4(HOGA1):c.700+9C>T rs375091787
NM_138413.4(HOGA1):c.708G>T (p.Val236=) rs61731946
NM_138413.4(HOGA1):c.752G>C (p.Cys251Ser) rs886047518
NM_138413.4(HOGA1):c.764G>A (p.Arg255Gln)
NM_138413.4(HOGA1):c.776C>T (p.Thr259Met)
NM_138413.4(HOGA1):c.828C>T (p.Asn276=) rs201683794
NM_138413.4(HOGA1):c.834G>T (p.Ala278=)
NM_138413.4(HOGA1):c.909C>T (p.Arg303=) rs764469579
NM_138413.4(HOGA1):c.910G>A (p.Ala304Thr) rs116527624
NM_138413.4(HOGA1):c.933C>T (p.Pro311=)

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.