NM_001130987.2(DYSF):c.5410G>A (p.Val1804Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002546124.2
Allele description [Variation Report for NM_001130987.2(DYSF):c.5410G>A (p.Val1804Met)]
NM_001130987.2(DYSF):c.5410G>A (p.Val1804Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
dnaJ homolog subfamily B member 6a [Trematomus bernacchii]
dnaJ homolog subfamily B member 6a [Trematomus bernacchii]gi|1838102309|ref|XP_033975783.1|Protein
-
Mus musculus tribbles homolog 1 (Drosophila) (Trib1), mRNA
Mus musculus tribbles homolog 1 (Drosophila) (Trib1), mRNAgi|142374770|ref|NM_144549.3|Nucleotide
-
hypothetical protein AXG93_638s1510 [Marchantia polymorpha subsp. ruderalis]
hypothetical protein AXG93_638s1510 [Marchantia polymorpha subsp. ruderalis]gi|1026767933|gb|OAE28161.1||gnl|WG J|AXG93_638s1510Protein
-
Interferon-induced protein with tetratricopeptide repeats 1 [Mus musculus]
Interferon-induced protein with tetratricopeptide repeats 1 [Mus musculus]gi|13277747|gb|AAH03768.1|Protein
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Last Updated: Sep 29, 2024