NM_001184.4(ATR):c.838C>A (p.Leu280Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004508157.1
Allele description [Variation Report for NM_001184.4(ATR):c.838C>A (p.Leu280Ile)]
NM_001184.4(ATR):c.838C>A (p.Leu280Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mixture/Component Compounds for PubChem Compound (Select 70392941... (2)
Mixture/Component Compounds for PubChem Compound (Select 70392941)SearchPubChem Compound
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024