NM_006015.6(ARID1A):c.299T>C (p.Leu100Pro) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003318913.1
Allele description [Variation Report for NM_006015.6(ARID1A):c.299T>C (p.Leu100Pro)]
NM_006015.6(ARID1A):c.299T>C (p.Leu100Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
sorting nexin-22 isoform X1 [Homo sapiens]
sorting nexin-22 isoform X1 [Homo sapiens]gi|530406470|ref|XP_005254734.1|Protein
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Last Updated: Aug 5, 2023