NM_001184.4(ATR):c.588G>T (p.Leu196Phe) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 7, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003301095.2
Allele description [Variation Report for NM_001184.4(ATR):c.588G>T (p.Leu196Phe)]
NM_001184.4(ATR):c.588G>T (p.Leu196Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Rattus norvegicus interleukin 11 (Il11), mRNA
Rattus norvegicus interleukin 11 (Il11), mRNAgi|2708392194|ref|NM_133519.6|Nucleotide
-
NT5M [Onychostruthus taczanowskii]
NT5M [Onychostruthus taczanowskii]Gene ID:121334457Gene
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Last Updated: May 7, 2024