NM_178857.6(RP1L1):c.498G>A (p.Gln166=) AND RP1L1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003968830.2
Allele description [Variation Report for NM_178857.6(RP1L1):c.498G>A (p.Gln166=)]
NM_178857.6(RP1L1):c.498G>A (p.Gln166=)
Condition(s)
- Name:
- RP1L1-related disorder
- Synonyms:
- RP1L1-related condition
- Identifiers:
-
Homo sapiens hypothetical protein FLJ10251 (FLJ10251), mRNA
Homo sapiens hypothetical protein FLJ10251 (FLJ10251), mRNAgi|8922310|ref|NM_018039.1|Nucleotide
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Last Updated: Oct 13, 2024