NM_003844.4(TNFRSF10A):c.891C>T (p.Asn297=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000884440.5
Allele description [Variation Report for NM_003844.4(TNFRSF10A):c.891C>T (p.Asn297=)]
NM_003844.4(TNFRSF10A):c.891C>T (p.Asn297=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024