NM_024334.3(TMEM43):c.51T>G (p.Val17=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 10, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000039384.5
Allele description [Variation Report for NM_024334.3(TMEM43):c.51T>G (p.Val17=)]
NM_024334.3(TMEM43):c.51T>G (p.Val17=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024