NM_001395002.1(MAP4K4):c.3232G>T (p.Ala1078Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002891669.2
Allele description [Variation Report for NM_001395002.1(MAP4K4):c.3232G>T (p.Ala1078Ser)]
NM_001395002.1(MAP4K4):c.3232G>T (p.Ala1078Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens family with sequence similarity 72 member A (FAM72A), transcript va...
Homo sapiens family with sequence similarity 72 member A (FAM72A), transcript variant 5, mRNAgi|1869284215|ref|NM_001385241.1|Nucleotide
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Last Updated: May 1, 2024