NM_032861.4(SERAC1):c.439A>C (p.Thr147Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002788961.2
Allele description [Variation Report for NM_032861.4(SERAC1):c.439A>C (p.Thr147Pro)]
NM_032861.4(SERAC1):c.439A>C (p.Thr147Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
hypothetical protein TGPRC2_203250 [Toxoplasma gondii TgCatPRC2]
hypothetical protein TGPRC2_203250 [Toxoplasma gondii TgCatPRC2]gi|1008944965|gb|KYK63637.1||gnl|WG P|cds.TGPRC2_203250Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024