NM_006031.6(PCNT):c.7404G>C (p.Gln2468His) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Mar 4, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000147199.7
Allele description [Variation Report for NM_006031.6(PCNT):c.7404G>C (p.Gln2468His)]
NM_006031.6(PCNT):c.7404G>C (p.Gln2468His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: May 19, 2024