NM_000018.4(ACADVL):c.1827+8T>C AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 7, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000440947.1
Allele description [Variation Report for NM_000018.4(ACADVL):c.1827+8T>C]
NM_000018.4(ACADVL):c.1827+8T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
LOC102724612 [Homo sapiens]
LOC102724612 [Homo sapiens]Gene ID:102724612Gene
-
102724612[uid] AND (alive[prop]) (1)
Gene
-
C19orf48 AND (alive[prop]) (46)
Gene
-
ZNF569 zinc finger protein 569 [Homo sapiens]
ZNF569 zinc finger protein 569 [Homo sapiens]Gene ID:148266Gene
-
148266[uid] AND (alive[prop]) (1)
Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Feb 28, 2024