NM_000271.5(NPC1):c.1221G>C (p.Gln407His) AND Niemann-Pick disease, type C1
- Germline classification:
- Uncertain significance (3 submissions)
- Last evaluated:
- Oct 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000765408.9
Allele description [Variation Report for NM_000271.5(NPC1):c.1221G>C (p.Gln407His)]
NM_000271.5(NPC1):c.1221G>C (p.Gln407His)
Condition(s)
- Name:
- Niemann-Pick disease, type C1
- Synonyms:
- NIEMANN-PICK DISEASE WITHOUT SPHINGOMYELINASE DEFICIENCY; Niemann-Pick disease with cholesterol esterification block; Niemann-Pick disease, chronic neuronopathic form; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009757; MedGen: C3179455; Orphanet: 646; OMIM: 257220
Assertion and evidence details
Last Updated: Apr 1, 2023