NM_018451.5(CENPJ):c.*639T>C AND Microcephaly 6, primary, autosomal recessive
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000364613.5
Allele description [Variation Report for NM_018451.5(CENPJ):c.*639T>C]
NM_018451.5(CENPJ):c.*639T>C
Condition(s)
-
LOC107985532 [Homo sapiens]
LOC107985532 [Homo sapiens]Gene ID:107985532Gene
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023