NM_001037.5(SCN1B):c.448+112G>A AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 24, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000171024.7
Allele description [Variation Report for NM_001037.5(SCN1B):c.448+112G>A]
NM_001037.5(SCN1B):c.448+112G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Xenopus laevis elongin C L homeolog (eloc.L), transcript variant X1, ...
PREDICTED: Xenopus laevis elongin C L homeolog (eloc.L), transcript variant X1, mRNAgi|2038224768|ref|XM_041565273.1|Nucleotide
-
PREDICTED: Homo sapiens C1q and TNF related 7 (C1QTNF7), transcript variant X3, ...
PREDICTED: Homo sapiens C1q and TNF related 7 (C1QTNF7), transcript variant X3, mRNAgi|2217348751|ref|XM_011513773.2|Nucleotide
-
dynein light chain 1, cytoplasmic isoform X2 [Cherax quadricarinatus]
dynein light chain 1, cytoplasmic isoform X2 [Cherax quadricarinatus]gi|2449285959|ref|XP_053650295.1|Protein
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Last Updated: Sep 29, 2024