NM_199334.5(THRA):c.302A>G (p.Lys101Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004668593.1
Allele description [Variation Report for NM_199334.5(THRA):c.302A>G (p.Lys101Arg)]
NM_199334.5(THRA):c.302A>G (p.Lys101Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
FCF1P4 FCF1 pseudogene 4 [Homo sapiens]
FCF1P4 FCF1 pseudogene 4 [Homo sapiens]Gene ID:106480799Gene
-
LOC127898088 [Homo sapiens]
LOC127898088 [Homo sapiens]Gene ID:127898088Gene
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024