NM_000423.3(KRT2):c.150C>T (p.Gly50=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001636881.8
Allele description [Variation Report for NM_000423.3(KRT2):c.150C>T (p.Gly50=)]
NM_000423.3(KRT2):c.150C>T (p.Gly50=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens coiled-coil domain containing 66 (CCDC66), transcript variant 24, n...
Homo sapiens coiled-coil domain containing 66 (CCDC66), transcript variant 24, non-coding RNAgi|1212990912|ref|NR_148374.1|Nucleotide
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Last Updated: Feb 28, 2024