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
-
cation transporter [Lactobacillus sp. HMSC17G08]
cation transporter [Lactobacillus sp. HMSC17G08]gi|1081166191|gb|OFT12657.1||gnl|WG O|HMPREF3068_12820Protein
-
hypothetical protein HMPREF3068_00080 [Lactobacillus sp. HMSC17G08]
hypothetical protein HMPREF3068_00080 [Lactobacillus sp. HMSC17G08]gi|1081173579|gb|OFT19688.1||gnl|WG O|HMPREF3068_00080Protein
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asparagine synthetase B [Lactobacillus sp. HMSC17G08]
asparagine synthetase B [Lactobacillus sp. HMSC17G08]gi|1081166182|gb|OFT12648.1||gnl|WG O|HMPREF3068_12775Protein
-
Homo sapiens sterile alpha motif domain containing 14, mRNA (cDNA clone MGC:1680...
Homo sapiens sterile alpha motif domain containing 14, mRNA (cDNA clone MGC:168097 IMAGE:9020474), complete cdsgi|223459645|gb|BC136485.1|Nucleotide
-
LOC127397875 [Homo sapiens]
LOC127397875 [Homo sapiens]Gene ID:127397875Gene
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Last Updated: May 1, 2024