NM_015475.5(FAM98A):c.774C>T (p.Ser258=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003425576.7
Allele description
NM_015475.5(FAM98A):c.774C>T (p.Ser258=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cDNA, FLJ98934
Homo sapiens cDNA, FLJ98934gi|164697210|dbj|AK308893.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jul 15, 2024