NM_001385641.1(SAMD11):c.1049C>T (p.Ser350Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001221928.4
Allele description [Variation Report for NM_001385641.1(SAMD11):c.1049C>T (p.Ser350Leu)]
NM_001385641.1(SAMD11):c.1049C>T (p.Ser350Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
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Last Updated: Feb 7, 2023