NM_000391.4(TPP1):c.465T>C (p.His155=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 6, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002315415.9
Allele description [Variation Report for NM_000391.4(TPP1):c.465T>C (p.His155=)]
NM_000391.4(TPP1):c.465T>C (p.His155=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
DC189306 Xenopus tropicalis embryo gastrula Xenopus tropicalis cDNA clone st91i1...
DC189306 Xenopus tropicalis embryo gastrula Xenopus tropicalis cDNA clone st91i15 5', mRNA sequencegi|119123151|gnl|dbEST|43388105|dbj 9306.1|Nucleotide
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Last Updated: Aug 18, 2024