NM_014000.3(VCL):c.20G>T (p.Arg7Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003442073.1
Allele description [Variation Report for NM_014000.3(VCL):c.20G>T (p.Arg7Leu)]
NM_014000.3(VCL):c.20G>T (p.Arg7Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Similar studies for GEO DataSets (Select 200029578) (19)
GEO DataSets
-
erbin isoform X6 [Homo sapiens]
erbin isoform X6 [Homo sapiens]gi|2217356387|ref|XP_047273337.1|Protein
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See more...Assertion and evidence details
Last Updated: Jun 2, 2024