NM_198859.4(PRICKLE2):c.1035C>G (p.Gly345=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Aug 12, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000387366.5
Allele description [Variation Report for NM_198859.4(PRICKLE2):c.1035C>G (p.Gly345=)]
NM_198859.4(PRICKLE2):c.1035C>G (p.Gly345=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024