NM_001876.4(CPT1A):c.1461C>T (p.Tyr487=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 30, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000424215.1
Allele description [Variation Report for NM_001876.4(CPT1A):c.1461C>T (p.Tyr487=)]
NM_001876.4(CPT1A):c.1461C>T (p.Tyr487=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens coiled-coil domain containing 115 (CCDC115), transcript variant 5, ...
Homo sapiens coiled-coil domain containing 115 (CCDC115), transcript variant 5, non-coding RNAgi|1676452991|ref|NR_135548.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024