NM_001614.5(ACTG1):c.735C>T (p.Gly245=) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 21, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001088638.7
Allele description [Variation Report for NM_001614.5(ACTG1):c.735C>T (p.Gly245=)]
NM_001614.5(ACTG1):c.735C>T (p.Gly245=)
Condition(s)
-
Homo sapiens AT rich interactive domain 1A (SWI- like) (ARID1A), transcript vari...
Homo sapiens AT rich interactive domain 1A (SWI- like) (ARID1A), transcript variant 2, mRNAgi|21264574|ref|NM_139135.1|Nucleotide
-
Mecodium gollmeri (0)
Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024