NM_138408.4(GTF3C6):c.399C>G (p.Phe133Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004183022.1
Allele description [Variation Report for NM_138408.4(GTF3C6):c.399C>G (p.Phe133Leu)]
NM_138408.4(GTF3C6):c.399C>G (p.Phe133Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens KCTD21 antisense RNA 1 (KCTD21-AS1), transcript variant 1, long non...
Homo sapiens KCTD21 antisense RNA 1 (KCTD21-AS1), transcript variant 1, long non-coding RNAgi|459447377|ref|NR_102280.1|Nucleotide
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Last Updated: Oct 13, 2024