NM_015473.4(HEATR5A):c.111G>C (p.Leu37Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004240015.1
Allele description [Variation Report for NM_015473.4(HEATR5A):c.111G>C (p.Leu37Phe)]
NM_015473.4(HEATR5A):c.111G>C (p.Leu37Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens EST from clone 27306, 5' end
Homo sapiens EST from clone 27306, 5' endgi|7799116|emb|AL355728.1|Nucleotide
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Last Updated: Oct 13, 2024