NM_017654.4(SAMD9):c.2071T>C (p.Trp691Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003163910.2
Allele description [Variation Report for NM_017654.4(SAMD9):c.2071T>C (p.Trp691Arg)]
NM_017654.4(SAMD9):c.2071T>C (p.Trp691Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
KH domain-containing protein 3 isoform 1 [Mus musculus]
KH domain-containing protein 3 isoform 1 [Mus musculus]gi|33468985|ref|NP_080166.1|Protein
-
RNA, Transfer, Amino Acid-Specific
RNA, Transfer, Amino Acid-SpecificA group of transfer RNAs which are specific for carrying each one of the 20 amino acids to the ribosome in preparation for protein synthesis.<br/>Year introduced: 1988MeSH
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Last Updated: Aug 25, 2024