NM_003798.4(CTNNAL1):c.983G>T (p.Arg328Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004374939.1
Allele description [Variation Report for NM_003798.4(CTNNAL1):c.983G>T (p.Arg328Leu)]
NM_003798.4(CTNNAL1):c.983G>T (p.Arg328Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens small NF90 (ILF3) associated RNA A14 (SNAR-A14), small nuclear RNA
Homo sapiens small NF90 (ILF3) associated RNA A14 (SNAR-A14), small nuclear RNAgi|209915631|ref|NR_024242.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024