NM_014141.6(CNTNAP2):c.1145G>A (p.Ser382Asn) AND History of neurodevelopmental disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000718421.2
Allele description
NM_014141.6(CNTNAP2):c.1145G>A (p.Ser382Asn)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
-
PREDICTED: Homo sapiens NCK adaptor protein 2 (NCK2), transcript variant X3, mRN...
PREDICTED: Homo sapiens NCK adaptor protein 2 (NCK2), transcript variant X3, mRNAgi|1034617124|ref|XM_017005104.1|Nucleotide
-
XM_039106778 (0)
GEO Profiles
-
XM_008771887 (0)
GEO Profiles
-
PREDICTED: Homo sapiens Fli-1 proto-oncogene, ETS transcription factor (FLI1), t...
PREDICTED: Homo sapiens Fli-1 proto-oncogene, ETS transcription factor (FLI1), transcript variant X2, mRNAgi|2217281855|ref|XM_017017406.2|Nucleotide
-
PREDICTED: Rattus norvegicus kinesin family member 16B (Kif16b), transcript vari...
PREDICTED: Rattus norvegicus kinesin family member 16B (Kif16b), transcript variant X2, mRNAgi|2678929566|ref|XM_006235108.5|Nucleotide
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Last Updated: Aug 23, 2022