NM_001953.5(TYMP):c.1126C>T (p.Arg376Trp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003251745.9
Allele description [Variation Report for NM_001953.5(TYMP):c.1126C>T (p.Arg376Trp)]
NM_001953.5(TYMP):c.1126C>T (p.Arg376Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus thymidylate synthase (Tyms), mRNA
Mus musculus thymidylate synthase (Tyms), mRNAgi|46358061|ref|NM_021288.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024