NM_018993.4(RIN2):c.217C>T (p.Arg73Trp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 28, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004027200.1
Allele description [Variation Report for NM_018993.4(RIN2):c.217C>T (p.Arg73Trp)]
NM_018993.4(RIN2):c.217C>T (p.Arg73Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Parcubacteria group bacterium GW2011_GWF2_42_7 16S ribosomal RNA gene, partial s...
Parcubacteria group bacterium GW2011_GWF2_42_7 16S ribosomal RNA gene, partial sequencegi|1118703787|gb|KX123700.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024