NM_000410.4(HFE):c.474A>G (p.Ala158=) AND Hereditary hemochromatosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003588682.1
Allele description [Variation Report for NM_000410.4(HFE):c.474A>G (p.Ala158=)]
NM_000410.4(HFE):c.474A>G (p.Ala158=)
Condition(s)
-
Homo sapiens
Homo sapiensThe Human Genome Project, currently maintained by the Genome Reference Consortium (GRC)BioProject
-
BioProject Links for Nucleotide (Select 568335875) (1)
BioProject
-
Homo sapiens Sharpr-MPRA regulatory region 5385 (LOC123956282) on chromosome 7
Homo sapiens Sharpr-MPRA regulatory region 5385 (LOC123956282) on chromosome 7gi|2184285389|ref|NG_078473.1|Nucleotide
-
eggc.vipeEx (0)
BioProject
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Last Updated: May 19, 2024