NM_000424.4(KRT5):c.1440-6T>C AND KRT5-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003913047.1
Allele description [Variation Report for NM_000424.4(KRT5):c.1440-6T>C]
NM_000424.4(KRT5):c.1440-6T>C
Condition(s)
- Name:
- KRT5-related disorder
- Synonyms:
- KRT5-related condition
- Identifiers:
-
Taxonomy Links for BioSample (Select 164232) (1)
Taxonomy
-
Homo sapiens chromosome 21, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 21, GRCh38.p14 Primary Assemblygi|568815577|gnl|ASM:GCF_000001305| f|NC_000021.9||gpp|GPC_000001313.1||gnl|NCBI_GENOMES|21Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 19, 2024