NM_000391.4(TPP1):c.1029G>C (p.Glu343Asp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002509307.1
Allele description [Variation Report for NM_000391.4(TPP1):c.1029G>C (p.Glu343Asp)]
NM_000391.4(TPP1):c.1029G>C (p.Glu343Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
homo sapiens[Organism] AND RAB11FIP3 AND (alive[prop]) (28)
Gene
-
homo sapiens[Organism] AND ASB15 AND (alive[prop]) (35)
Gene
-
OMIM Links for GEO Profiles (Select 87938762) (1)
OMIM
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See more...Assertion and evidence details
Last Updated: Mar 10, 2024