NM_001927.4(DES):c.1411T>C (p.Ter471Gln) AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Aug 4, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000296486.4
Allele description [Variation Report for NM_001927.4(DES):c.1411T>C (p.Ter471Gln)]
NM_001927.4(DES):c.1411T>C (p.Ter471Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens wingless-type MMTV integration site family, member 5B, mRNA (cDNA c...
Homo sapiens wingless-type MMTV integration site family, member 5B, mRNA (cDNA clone MGC:2648 IMAGE:3528819), complete cdsgi|12804648|gb|BC001749.1|Nucleotide
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Last Updated: Sep 29, 2024