NM_000188.3(HK1):c.1348G>C (p.Gly450Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001880139.5
Allele description [Variation Report for NM_000188.3(HK1):c.1348G>C (p.Gly450Arg)]
NM_000188.3(HK1):c.1348G>C (p.Gly450Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Homo sapiens opsin 1 (cone pigments), long-wave-sensitive (color blindness, protan) (OPN1LW), mRNAgi|56550111|ref|NM_020061.2|Nucleotide
-
Rattus norvegicus cDNA clone IMAGE:7382543
Rattus norvegicus cDNA clone IMAGE:7382543gi|71051907|gb|BC099171.1|Nucleotide
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Last Updated: May 1, 2024