NM_016356.5(DCDC2):c.1313G>T (p.Ser438Ile) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002796214.2
Allele description [Variation Report for NM_016356.5(DCDC2):c.1313G>T (p.Ser438Ile)]
NM_016356.5(DCDC2):c.1313G>T (p.Ser438Ile)
Condition(s)
-
nesprin-2 isoform X19 [Homo sapiens]
nesprin-2 isoform X19 [Homo sapiens]gi|767980098|ref|XP_011534886.1|Protein
-
txid4577[orgn] AND "cultivar IL101"[All Fields] (31)
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Last Updated: Feb 28, 2024