NM_000831.4(GRIK3):c.17G>A (p.Arg6Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004393825.1
Allele description [Variation Report for NM_000831.4(GRIK3):c.17G>A (p.Arg6Gln)]
NM_000831.4(GRIK3):c.17G>A (p.Arg6Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens purinergic receptor P2Y14 (P2RY14), transcript variant X...
PREDICTED: Homo sapiens purinergic receptor P2Y14 (P2RY14), transcript variant X2, mRNAgi|2462594236|ref|XM_054348644.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024