NM_000322.5(PRPH2):c.483C>T (p.Ile161=) AND Patterned macular dystrophy 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001161379.5
Allele description [Variation Report for NM_000322.5(PRPH2):c.483C>T (p.Ile161=)]
NM_000322.5(PRPH2):c.483C>T (p.Ile161=)
Condition(s)
-
os15h06.x5 NCI_CGAP_Kid5 Homo sapiens cDNA clone IMAGE:1605467 3', mRNA sequence
os15h06.x5 NCI_CGAP_Kid5 Homo sapiens cDNA clone IMAGE:1605467 3', mRNA sequencegi|5439734|gnl|dbEST|2908275|gb|AI8 .1|Nucleotide
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Last Updated: Sep 29, 2024