NM_001370466.1(NOD2):c.2693A>G (p.Asp898Gly) AND Inborn genetic diseases
- 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:
- RCV002534429.9
Allele description [Variation Report for NM_001370466.1(NOD2):c.2693A>G (p.Asp898Gly)]
NM_001370466.1(NOD2):c.2693A>G (p.Asp898Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus calmodulin regulated spectrin-associated protein 1-like 1, mRNA (cD...
Mus musculus calmodulin regulated spectrin-associated protein 1-like 1, mRNA (cDNA clone IMAGE:30729835)gi|72679433|gb|BC100407.1|Nucleotide
-
PGM1 phosphoglucomutase 1 [Bos taurus]
PGM1 phosphoglucomutase 1 [Bos taurus]Gene ID:534402Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 20, 2024