NM_001037.5(SCN1B):c.448+88G>A AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000171062.21
Allele description [Variation Report for NM_001037.5(SCN1B):c.448+88G>A]
NM_001037.5(SCN1B):c.448+88G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens ventral anterior homeobox 2 (VAX2), mRNA
Homo sapiens ventral anterior homeobox 2 (VAX2), mRNAgi|7110734|ref|NM_012476.1|Nucleotide
-
txid2848431[Organism:noexp] (1)
SRA
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Last Updated: Sep 8, 2024