NM_001077418.3(TMEM231):c.140-15C>T AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000878145.9
Allele description [Variation Report for NM_001077418.3(TMEM231):c.140-15C>T]
NM_001077418.3(TMEM231):c.140-15C>T
Condition(s)
-
Homo sapiens chromosome 12, whole genome shotgun sequence
Homo sapiens chromosome 12, whole genome shotgun sequencegi|512322331|gnl|WGS:AMYH|chr12|gb| 620.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024