NM_212482.4(FN1):c.5798C>G (p.Thr1933Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003266301.2
Allele description [Variation Report for NM_212482.4(FN1):c.5798C>G (p.Thr1933Ser)]
NM_212482.4(FN1):c.5798C>G (p.Thr1933Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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acetylcholine receptor subunit alpha [Scleropages formosus]
acetylcholine receptor subunit alpha [Scleropages formosus]gi|1083447773|ref|XP_018585183.1|Protein
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BJ085053 NIBB Mochii normalized Xenopus tailbud library Xenopus laevis cDNA clon...
BJ085053 NIBB Mochii normalized Xenopus tailbud library Xenopus laevis cDNA clone XL102i20 3', mRNA sequencegi|17580885|gnl|dbEST|10553368|dbj| 053.1|Nucleotide
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Last Updated: May 1, 2024