NM_130849.4(SLC39A4):c.1240T>C (p.Phe414Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004461555.1
Allele description [Variation Report for NM_130849.4(SLC39A4):c.1240T>C (p.Phe414Leu)]
NM_130849.4(SLC39A4):c.1240T>C (p.Phe414Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Capnocytophaga cynodegmi strain G7591 chromosome, complete genome
Capnocytophaga cynodegmi strain G7591 chromosome, complete genomegi|1242546331|gb|CP022378.1|Nucleotide
-
Capnocytophaga canimorsus strain H3936 chromosome, complete genome
Capnocytophaga canimorsus strain H3936 chromosome, complete genomegi|1242572053|gb|CP022389.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024