NM_016284.5(CNOT1):c.5895+4T>C AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002829992.2
Allele description [Variation Report for NM_016284.5(CNOT1):c.5895+4T>C]
NM_016284.5(CNOT1):c.5895+4T>C
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
mospd1 motile sperm domain containing 1 [Danio rerio]
mospd1 motile sperm domain containing 1 [Danio rerio]Gene ID:406678Gene
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uncharacterized protein LOC101214681 [Cucumis sativus]
uncharacterized protein LOC101214681 [Cucumis sativus]gi|449469466|ref|XP_004152441.1|Protein
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peroxisomal adenine nucleotide carrier 1-like [Cucumis melo var. makuwa]
peroxisomal adenine nucleotide carrier 1-like [Cucumis melo var. makuwa]gi|1735219918|gb|KAA0061712.1||gnl| STE|E6C27_scaffold212G00860Protein
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hypothetical protein F3B15_25050, partial [Salmonella enterica subsp. enterica s...
hypothetical protein F3B15_25050, partial [Salmonella enterica subsp. enterica serovar Typhi]gb|NRJ45860.1||gnl|WGS:VZQR|F3B15_2Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024