NM_000261.2(MYOC):c.855G>T (p.Thr285=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 6, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000177024.12
Allele description [Variation Report for NM_000261.2(MYOC):c.855G>T (p.Thr285=)]
NM_000261.2(MYOC):c.855G>T (p.Thr285=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens phosphodiesterase 6B (PDE6B), transcript variant X11, mR...
PREDICTED: Homo sapiens phosphodiesterase 6B (PDE6B), transcript variant X11, mRNAgi|2462597508|ref|XM_054350170.1|Nucleotide
-
Homo sapiens phosphodiesterase 6B (PDE6B), transcript variant 1, mRNA
Homo sapiens phosphodiesterase 6B (PDE6B), transcript variant 1, mRNAgi|1824670925|ref|NM_000283.4|Nucleotide
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Last Updated: Oct 13, 2024