NM_020366.4(RPGRIP1):c.127C>T (p.Arg43Trp) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001856476.4
Allele description [Variation Report for NM_020366.4(RPGRIP1):c.127C>T (p.Arg43Trp)]
NM_020366.4(RPGRIP1):c.127C>T (p.Arg43Trp)
Condition(s)
-
Homo sapiens proopiomelanocortin (POMC), transcript variant 1, mRNA
Homo sapiens proopiomelanocortin (POMC), transcript variant 1, mRNAgi|1889539314|ref|NM_001035256.3|Nucleotide
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Last Updated: Sep 29, 2024