NM_000827.4(GRIA1):c.1453-4_1453-3insTTTC AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002678700.2
Allele description [Variation Report for NM_000827.4(GRIA1):c.1453-4_1453-3insTTTC]
NM_000827.4(GRIA1):c.1453-4_1453-3insTTTC
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Pseudoalteromonas sp. PY145D 16S ribosomal RNA gene, partial sequence
Pseudoalteromonas sp. PY145D 16S ribosomal RNA gene, partial sequencegi|225032586|gb|FJ799030.1|Nucleotide
-
eggc.vipXje (0)
BioProject
-
zinc finger protein 42 (myeloid-specific retinoic acid-responsive), isoform CRA_...
zinc finger protein 42 (myeloid-specific retinoic acid-responsive), isoform CRA_a [Homo sapiens]gi|119593022|gb|EAW72616.1||gnl|WGS |hCP1875100Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024