NM_015516.4(TSKU):c.671C>T (p.Ala224Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004476565.1
Allele description [Variation Report for NM_015516.4(TSKU):c.671C>T (p.Ala224Val)]
NM_015516.4(TSKU):c.671C>T (p.Ala224Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens Gfo/Idh/MocA-like oxidoreductase domain containing 3, pseudogene (G...
Homo sapiens Gfo/Idh/MocA-like oxidoreductase domain containing 3, pseudogene (GFOD3P), transcript variant 4, non-coding RNAgi|297747264|ref|NR_033708.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024