NM_001397246.1(PVRIG):c.445C>T (p.Arg149Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004215024.1
Allele description [Variation Report for NM_001397246.1(PVRIG):c.445C>T (p.Arg149Trp)]
NM_001397246.1(PVRIG):c.445C>T (p.Arg149Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
LOC107986463 [Homo sapiens]
LOC107986463 [Homo sapiens]Gene ID:107986463Gene
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Last Updated: Oct 8, 2024