NM_014141.6(CNTNAP2):c.1078A>G (p.Asn360Asp) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003343678.2
Allele description [Variation Report for NM_014141.6(CNTNAP2):c.1078A>G (p.Asn360Asp)]
NM_014141.6(CNTNAP2):c.1078A>G (p.Asn360Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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BLISS_shNT_rep1
BLISS_shNT_rep1biosample
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Nakaseomyces glabratus
Nakaseomyces glabratusNakaseomyces glabratus RefSeq Genome sequencing and assemblyBioProject
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Cardamine graeca isolate M10 internal transcribed spacer 1, partial sequence; 5....
Cardamine graeca isolate M10 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequencegi|215513724|gb|FJ384197.1|Nucleotide
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Cardamine graeca isolate J411 internal transcribed spacer 1, partial sequence; 5...
Cardamine graeca isolate J411 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequencegi|215513722|gb|FJ384195.1|Nucleotide
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Last Updated: Sep 29, 2024