NM_198488.5(FAM83H):c.1435G>C (p.Gly479Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003207944.2
Allele description [Variation Report for NM_198488.5(FAM83H):c.1435G>C (p.Gly479Arg)]
NM_198488.5(FAM83H):c.1435G>C (p.Gly479Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
eggc.vipo45 (0)
BioProject
-
(eggc.vip) AND TxO (0)
BioProject
-
eggc.vipRov (0)
BioProject
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Last Updated: May 1, 2024