NM_001142966.3(GREB1L):c.1062A>G (p.Ser354=) AND GREB1L-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 10, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003916707.2
Allele description [Variation Report for NM_001142966.3(GREB1L):c.1062A>G (p.Ser354=)]
NM_001142966.3(GREB1L):c.1062A>G (p.Ser354=)
Condition(s)
- Name:
- GREB1L-related disorder
- Synonyms:
- GREB1L-related condition
- Identifiers:
-
neurotrophin-3 isoform 2 preproprotein [Homo sapiens]
neurotrophin-3 isoform 2 preproprotein [Homo sapiens]gi|4505469|ref|NP_002518.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 8, 2024