NM_001170629.2(CHD8):c.2907+18T>C AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003567528.2
Allele description [Variation Report for NM_001170629.2(CHD8):c.2907+18T>C]
NM_001170629.2(CHD8):c.2907+18T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
BX106051 NCI_CGAP_Co16 Homo sapiens cDNA clone IMAGp998E235947; IMAGE:2394238 5'...
BX106051 NCI_CGAP_Co16 Homo sapiens cDNA clone IMAGp998E235947; IMAGE:2394238 5', mRNA sequencegi|27833866|gnl|dbEST|16739684|emb| 051.1|Nucleotide
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Last Updated: Sep 29, 2024