NM_007327.4(GRIN1):c.2723C>G (p.Ala908Gly) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 26, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001755194.2
Allele description [Variation Report for NM_007327.4(GRIN1):c.2723C>G (p.Ala908Gly)]
NM_007327.4(GRIN1):c.2723C>G (p.Ala908Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Menin is a ‘reader’ of histone H3 lysine 79 methylation (ChIP-Seq)
Menin is a ‘reader’ of histone H3 lysine 79 methylation (ChIP-Seq)Menin is a ‘reader’ of histone H3 lysine 79 methylation (ChIP-Seq)BioProject
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023