NM_002139.4(RBMX):c.891A>G (p.Thr297=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000455488.4
Allele description [Variation Report for NM_002139.4(RBMX):c.891A>G (p.Thr297=)]
NM_002139.4(RBMX):c.891A>G (p.Thr297=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 26, 2023