NM_006269.2(RP1):c.1732G>T (p.Glu578Ter) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Aug 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001953777.3
Allele description [Variation Report for NM_006269.2(RP1):c.1732G>T (p.Glu578Ter)]
NM_006269.2(RP1):c.1732G>T (p.Glu578Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
H.sapiens CMRF35 mRNA, complete CDS
H.sapiens CMRF35 mRNA, complete CDSgi|396169|emb|X66171.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024