NM_005560.6(LAMA5):c.10960G>A (p.Val3654Met) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003240862.2
Allele description [Variation Report for NM_005560.6(LAMA5):c.10960G>A (p.Val3654Met)]
NM_005560.6(LAMA5):c.10960G>A (p.Val3654Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
uncharacterized protein [Danio rerio]
uncharacterized protein [Danio rerio]gi|528507831|ref|XP_005159145.1|Protein
-
PREDICTED: Homo sapiens solute carrier family 1 member 1 (SLC1A1), transcript va...
PREDICTED: Homo sapiens solute carrier family 1 member 1 (SLC1A1), transcript variant X4, mRNAgi|2462625953|ref|XM_054363569.1|Nucleotide
-
MAG: hypothetical protein AUJ31_00060 [Parcubacteria group bacterium CG1_02_39_1...
MAG: hypothetical protein AUJ31_00060 [Parcubacteria group bacterium CG1_02_39_15]gi|1101087424|gb|OIO47236.1||gnl|WG E|AUJ31_00060Protein
-
Chain f, NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrial
Chain f, NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrialgi|2431413579|pdb|7W4Q|fProtein
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Last Updated: May 1, 2024