NM_014748.4(SNX17):c.644T>C (p.Met215Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004141868.1
Allele description [Variation Report for NM_014748.4(SNX17):c.644T>C (p.Met215Thr)]
NM_014748.4(SNX17):c.644T>C (p.Met215Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Jun 9, 2024