NM_003742.4(ABCB11):c.3767C>T (p.Thr1256Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003320963.1
Allele description [Variation Report for NM_003742.4(ABCB11):c.3767C>T (p.Thr1256Met)]
NM_003742.4(ABCB11):c.3767C>T (p.Thr1256Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 19, 2023