NM_000062.3(SERPING1):c.1499C>T (p.Ala500Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002022672.3
Allele description [Variation Report for NM_000062.3(SERPING1):c.1499C>T (p.Ala500Val)]
NM_000062.3(SERPING1):c.1499C>T (p.Ala500Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Rhinolophus hipposideros genome assembly, chromosome: 25
Rhinolophus hipposideros genome assembly, chromosome: 25gi|2750966755|emb|OZ077442.1|Nucleotide
-
Rhinolophus hipposideros genome assembly, organelle: mitochondrion
Rhinolophus hipposideros genome assembly, organelle: mitochondriongi|2750966768|emb|OZ077446.1|Nucleotide
-
Rhinolophus hipposideros genome assembly, chromosome: 10
Rhinolophus hipposideros genome assembly, chromosome: 10gi|2750966413|emb|OZ077427.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024