NM_000914.5(OPRM1):c.515G>A (p.Cys172Tyr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004104048.1
Allele description [Variation Report for NM_000914.5(OPRM1):c.515G>A (p.Cys172Tyr)]
NM_000914.5(OPRM1):c.515G>A (p.Cys172Tyr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
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Homo sapiens solute carrier family 30 member 8 (SLC30A8), transcript variant 1, ...
Homo sapiens solute carrier family 30 member 8 (SLC30A8), transcript variant 1, mRNAgi|64762488|ref|NM_173851.2|Nucleotide
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Leviprora inops
Leviprora inopsLeviprora inops (Longhead Flathead), fLevIno1, sequence dataBioProject
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024