NM_001135196.2(C10orf71):c.633G>T (p.Gln211His) AND not provided
- Germline classification:
- Benign (1 submission)
- 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:
- RCV000959913.4
Allele description [Variation Report for NM_001135196.2(C10orf71):c.633G>T (p.Gln211His)]
NM_001135196.2(C10orf71):c.633G>T (p.Gln211His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
txid1392[orgn] (1)
Genome
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Last Updated: Dec 24, 2023