NM_000258.3(MYL3):c.69C>T (p.Pro23=) AND not specified
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Oct 28, 2006
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000036033.14
Allele description [Variation Report for NM_000258.3(MYL3):c.69C>T (p.Pro23=)]
NM_000258.3(MYL3):c.69C>T (p.Pro23=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
OMIM Links for GEO Profiles (Select 105779324) (1)
OMIM
-
Nucleotide INSDC for Assembly (Select 46519058) (0)
Nucleotide
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Last Updated: May 7, 2024