NM_000324.3(RHAG):c.1165G>A (p.Gly389Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003130409.3
Allele description [Variation Report for NM_000324.3(RHAG):c.1165G>A (p.Gly389Arg)]
NM_000324.3(RHAG):c.1165G>A (p.Gly389Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens Nik related kinase (NRK), transcript variant X1, mRNA
PREDICTED: Homo sapiens Nik related kinase (NRK), transcript variant X1, mRNAgi|2462628628|ref|XM_054326657.1|Nucleotide
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Last Updated: Mar 16, 2024