NM_001010915.5(HACD4):c.292C>T (p.Leu98Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 12, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004627372.1
Allele description [Variation Report for NM_001010915.5(HACD4):c.292C>T (p.Leu98Phe)]
NM_001010915.5(HACD4):c.292C>T (p.Leu98Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
protein FAM3A isoform X1 [Rattus norvegicus]
protein FAM3A isoform X1 [Rattus norvegicus]gi|2678976569|ref|XP_063136329.1|Protein
-
NEDD8-conjugating enzyme Ubc12 [Homo sapiens]
NEDD8-conjugating enzyme Ubc12 [Homo sapiens]gi|4507791|ref|NP_003960.1|Protein
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024