NM_001271208.2(NEB):c.18431A>G (p.His6144Arg) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 24, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000606436.1
Allele description
NM_001271208.2(NEB):c.18431A>G (p.His6144Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 13, 2021