NM_000545.8(HNF1A):c.767C>T (p.Ser256Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 14, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000516404.3
Allele description [Variation Report for NM_000545.8(HNF1A):c.767C>T (p.Ser256Phe)]
NM_000545.8(HNF1A):c.767C>T (p.Ser256Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens armadillo repeat containing X-linked 3 (ARMCX3), RefSeqGene on chro...
Homo sapiens armadillo repeat containing X-linked 3 (ARMCX3), RefSeqGene on chromosome Xgi|2296125312|ref|NG_013222.2|Nucleotide
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Last Updated: Jun 23, 2024