NM_000183.3(HADHB):c.1389+10A>G AND Mitochondrial trifunctional protein deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003621192.2
Allele description [Variation Report for NM_000183.3(HADHB):c.1389+10A>G]
NM_000183.3(HADHB):c.1389+10A>G
Condition(s)
-
PREDICTED: similar to allantoicase, partial [Strongylocentrotus purpuratus]
PREDICTED: similar to allantoicase, partial [Strongylocentrotus purpuratus]gi|115679015|ref|XP_781878.2|Protein
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Last Updated: Sep 29, 2024