NM_020989.4(CRYGC):c.220G>A (p.Asp74Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002924787.2
Allele description [Variation Report for NM_020989.4(CRYGC):c.220G>A (p.Asp74Asn)]
NM_020989.4(CRYGC):c.220G>A (p.Asp74Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Mus musculus olfactory receptor family 5 subfamily P member 55 (Or5p55), mRNA
Mus musculus olfactory receptor family 5 subfamily P member 55 (Or5p55), mRNAgi|49227562|ref|NM_146924.1|Nucleotide
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CIT-HSP-2379D16.TR CIT-HSP Homo sapiens genomic clone 2379D16, genomic survey se...
CIT-HSP-2379D16.TR CIT-HSP Homo sapiens genomic clone 2379D16, genomic survey sequencegi|3489628|gnl|dbGSS|213744|gb|AQ11 1|Nucleotide
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NCSC5A10T3 Subtracted Conidial Neurospora crassa cDNA clone SC5A10 5', mRNA sequ...
NCSC5A10T3 Subtracted Conidial Neurospora crassa cDNA clone SC5A10 5', mRNA sequencegi|4240646|gnl|dbEST|2205288|gb|AI3 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024