NM_000037.4(ANK1):c.2960+1G>A AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Nov 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001509341.5
Allele description [Variation Report for NM_000037.4(ANK1):c.2960+1G>A]
NM_000037.4(ANK1):c.2960+1G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens complement C6 (C6), transcript variant X2, mRNA
PREDICTED: Homo sapiens complement C6 (C6), transcript variant X2, mRNAgi|2217357219|ref|XM_011514115.4|Nucleotide
-
PREDICTED: Homo sapiens complement C6 (C6), transcript variant X1, mRNA
PREDICTED: Homo sapiens complement C6 (C6), transcript variant X1, mRNAgi|2217357218|ref|XM_011514114.4|Nucleotide
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Last Updated: Mar 16, 2024