NM_001164277.2(SLC37A4):c.497G>A (p.Arg166His) AND SLC37A4-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003955196.2
Allele description [Variation Report for NM_001164277.2(SLC37A4):c.497G>A (p.Arg166His)]
NM_001164277.2(SLC37A4):c.497G>A (p.Arg166His)
Condition(s)
- Name:
- SLC37A4-related disorder
- Synonyms:
- SLC37A4-related condition
- Identifiers:
-
Homo sapiens ZFP14 zinc finger protein (ZFP14), transcript variant 2, mRNA
Homo sapiens ZFP14 zinc finger protein (ZFP14), transcript variant 2, mRNAgi|307133708|ref|NM_020917.2|Nucleotide
-
Homo sapiens cDNA FLJ54557 complete cds, highly similar to helicase MOV-10 (EC 3...
Homo sapiens cDNA FLJ54557 complete cds, highly similar to helicase MOV-10 (EC 3.6.1.-)gi|221043517|dbj|AK301229.1|Nucleotide
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Last Updated: Oct 13, 2024