NM_012210.4(TRIM32):c.474A>G (p.Glu158=) AND Bardet-Biedl syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001505827.7
Allele description [Variation Report for NM_012210.4(TRIM32):c.474A>G (p.Glu158=)]
NM_012210.4(TRIM32):c.474A>G (p.Glu158=)
Condition(s)
-
Homo sapiens calsenilin, presenilin binding protein, EF hand transcription facto...
Homo sapiens calsenilin, presenilin binding protein, EF hand transcription factor (CSEN), mRNAgi|21361445|ref|NM_013434.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024