NM_001366385.1(CARD14):c.2544C>G (p.Leu848=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003804427.2
Allele description [Variation Report for NM_001366385.1(CARD14):c.2544C>G (p.Leu848=)]
NM_001366385.1(CARD14):c.2544C>G (p.Leu848=)
Condition(s)
-
NADH dehydrogenase subunit II (mitochondrion) [Sturnella sp.]
NADH dehydrogenase subunit II (mitochondrion) [Sturnella sp.]gi|2065956455|gb|QXM27334.1|Protein
-
PREDICTED: Homo sapiens mediator complex subunit 13L (MED13L), transcript varian...
PREDICTED: Homo sapiens mediator complex subunit 13L (MED13L), transcript variant X3, mRNAgi|2217288309|ref|XM_047428607.1|Nucleotide
-
muscle-specific tyrosine kinase, partial [Sturnella loyca]
muscle-specific tyrosine kinase, partial [Sturnella loyca]gi|343202239|gb|AEM06261.1|Protein
-
cytochrome oxidase subunit I, partial (mitochondrion) [Sturnella loyca]
cytochrome oxidase subunit I, partial (mitochondrion) [Sturnella loyca]gi|1131508550|gb|APU89666.1|Protein
-
ATP synthase F0 subunit 6 (mitochondrion) [Sturnella neglecta]
ATP synthase F0 subunit 6 (mitochondrion) [Sturnella neglecta]gi|208964795|gb|ACI31614.1|Protein
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Last Updated: Sep 29, 2024