NM_006493.4(CLN5):c.87C>G (p.Ala29=) AND not specified
- Germline classification:
- Benign (7 submissions)
- Last evaluated:
- Jul 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000081416.31
Allele description [Variation Report for NM_006493.4(CLN5):c.87C>G (p.Ala29=)]
NM_006493.4(CLN5):c.87C>G (p.Ala29=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens c-Maf inducing protein (CMIP), transcript variant X3, mR...
PREDICTED: Homo sapiens c-Maf inducing protein (CMIP), transcript variant X3, mRNAgi|2217307664|ref|XM_005256179.6|Nucleotide
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Last Updated: Jun 9, 2024