NM_015272.5(RPGRIP1L):c.999T>G (p.Ser333=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 11, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002499486.1
Allele description [Variation Report for NM_015272.5(RPGRIP1L):c.999T>G (p.Ser333=)]
NM_015272.5(RPGRIP1L):c.999T>G (p.Ser333=)
Condition(s)
-
Homo sapiens DMRT like family C1 (DMRTC1), transcript variant 4, non-coding RNA
Homo sapiens DMRT like family C1 (DMRTC1), transcript variant 4, non-coding RNAgi|1904926806|ref|NR_170342.1|Nucleotide
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Last Updated: Oct 13, 2024