NM_000424.4(KRT5):c.1439+6T>C AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003739256.1
Allele description [Variation Report for NM_000424.4(KRT5):c.1439+6T>C]
NM_000424.4(KRT5):c.1439+6T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
transcription factor Gibbin isoform X1 [Homo sapiens]
transcription factor Gibbin isoform X1 [Homo sapiens]gi|767903789|ref|XP_011539557.1|Protein
-
Human DNA sequence from clone RP1-159A19 on chromosome 1p36.13, complete sequenc...
Human DNA sequence from clone RP1-159A19 on chromosome 1p36.13, complete sequencegi|5262302|emb|AL031729.16|Nucleotide
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Last Updated: Feb 28, 2024