NM_000110.4(DPYD):c.1390G>A (p.Val464Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002751796.2
Allele description [Variation Report for NM_000110.4(DPYD):c.1390G>A (p.Val464Ile)]
NM_000110.4(DPYD):c.1390G>A (p.Val464Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
HAMP domain-containing methyl-accepting chemotaxis protein (plasmid) [Shinella o...
HAMP domain-containing methyl-accepting chemotaxis protein (plasmid) [Shinella oryzae]gi|2225498808|gnl|PRJNA756894|K6301 0|gb|UPA27813.1|Protein
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PTS system, cellobiose-specific IIC component [Clostridium isatidis]
PTS system, cellobiose-specific IIC component [Clostridium isatidis]gi|1239644592|gnl|PRJNA335982|BEN51 5|gb|ASW42403.1|Protein
-
LOC115199972 [Salmo trutta]
LOC115199972 [Salmo trutta]Gene ID:115199972Gene
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Last Updated: May 1, 2024