NM_000311.5(PRNP):c.204T>C (p.Pro68=) AND Inherited prion disease
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000383267.5
Allele description [Variation Report for NM_000311.5(PRNP):c.204T>C (p.Pro68=)]
NM_000311.5(PRNP):c.204T>C (p.Pro68=)
Condition(s)
- Name:
- Inherited prion disease
- Identifiers:
- MedGen: C5679775
-
Lepophidium jeannae Zic family member 1 (zic1) gene, partial cds
Lepophidium jeannae Zic family member 1 (zic1) gene, partial cdsgi|482715125|gb|KC831117.1|Nucleotide
-
Lepophidium profundorum isolate MM12 small subunit ribosomal RNA gene, partial s...
Lepophidium profundorum isolate MM12 small subunit ribosomal RNA gene, partial sequence; mitochondrialgi|1788585343|gb|MN883196.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024