NM_019843.4(EIF4ENIF1):c.2159A>T (p.Lys720Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004312746.1
Allele description [Variation Report for NM_019843.4(EIF4ENIF1):c.2159A>T (p.Lys720Ile)]
NM_019843.4(EIF4ENIF1):c.2159A>T (p.Lys720Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens chromosome 16 clone RP11-109D24, complete sequence
Homo sapiens chromosome 16 clone RP11-109D24, complete sequencegi|21954994|gnl|lanlchgs|109D24|gb| 125.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024