NM_001769.4(CD9):c.286C>T (p.Leu96Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004435579.1
Allele description [Variation Report for NM_001769.4(CD9):c.286C>T (p.Leu96Phe)]
NM_001769.4(CD9):c.286C>T (p.Leu96Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
LRG_1189t1 (0)
Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024