Table 7.

Juvenile Hemochromatosis: Notable Pathogenic Variants by Gene

Gene 1

Reference SequencesDNA Nucleotide ChangePredicted Protein Change
(Alias 2)
Comment [Reference]
HAMP NM_021175​.4
NP_066998​.1
c.166C>Tp.Arg56TerPathogenic variants that occur in known functional domains [Roetto et al 2003; Delatycki et al 2004; Jacolot et al 2004; Roetto et al 2004; Badar et al 2016; Author, unpublished data]
c.175C>Gp.Arg59Gly
c.175C>Tp.Arg59Ter
c.176G>Cp.Arg59Pro
c.208T>Cp.Cys70Arg
c.233G>Ap.Cys78Tyr
HJV NM_213653​.3
NP_998818​.1
c.959G>Tp.Gly320ValMost prevalent pathogenic variant reported to date [Kong et al 2019]
c.295G>Ap.Gly99ArgRecurrent pathogenic variants in northern European individuals [Lanzara et al 2004, Hamdi-Rozé et al 2019]
c.302T>Cp.Leu101Pro
c.445delGp.Asp149fs
(p.Asp149ThrfsTer97)
Recurrent pathogenic variant in Italian individuals [Lanzara et al 2004]
c.526C>Tp.Arg176CysPathogenic variant recurrent in French individuals [Hamdi-Rozé et al 2019]
c.745G>Cp.Asp249HisMost common pathogenic variant in Japanese individuals [Ikuta et al 2017]
c.934C>Tp.Gln312TerPredominant pathogenic variant in Japanese; recurrent in Chinese individuals [Ikuta et al 2017]
c.962_963delGCinsAAp.Cys321TerMost common pathogenic variant in Chinese population [Lv et al 2018]
c.1006G>Tp.Gly336TerPathogenic variant recurrent in Indian population [Dhillon et al 2018]

Variants listed in the table have been provided by the authors. GeneReviews staff have not independently verified the classification of variants.

GeneReviews follows the standard naming conventions of the Human Genome Variation Society (varnomen​.hgvs.org). See Quick Reference for an explanation of nomenclature.

1.

Genes from Table 1 in alphabetic order

2.

Variant designation that does not conform to current naming conventions

From: Juvenile Hemochromatosis

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