NM_001034853.2(RPGR):c.2777_2778del (p.Glu926fs) AND Retinitis pigmentosa 3
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Dec 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002463461.3
Allele description [Variation Report for NM_001034853.2(RPGR):c.2777_2778del (p.Glu926fs)]
NM_001034853.2(RPGR):c.2777_2778del (p.Glu926fs)
Condition(s)
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Homo sapiens cDNA clone IMAGE:4388353
Homo sapiens cDNA clone IMAGE:4388353gi|21707482|gb|BC033834.1|Nucleotide
-
AGENCOURT_6542488 NIH_MGC_119 Homo sapiens cDNA clone IMAGE:5742683 5', mRNA seq...
AGENCOURT_6542488 NIH_MGC_119 Homo sapiens cDNA clone IMAGE:5742683 5', mRNA sequencegi|18791048|gnl|dbEST|11125227|gb|B 40.1|Nucleotide
-
Homo sapiens solute carrier family 25, member 37, mRNA (cDNA clone MGC:164430 IM...
Homo sapiens solute carrier family 25, member 37, mRNA (cDNA clone MGC:164430 IMAGE:40146821), complete cdsgi|124376585|gb|BC132799.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024