NM_015065.3(EXPH5):c.2588A>T (p.Lys863Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003369785.2
Allele description [Variation Report for NM_015065.3(EXPH5):c.2588A>T (p.Lys863Ile)]
NM_015065.3(EXPH5):c.2588A>T (p.Lys863Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Spermophilus parryii UAM:Mamm:35165 chromosomal copy 2 anonymous locus SppaALP6 ...
Spermophilus parryii UAM:Mamm:35165 chromosomal copy 2 anonymous locus SppaALP6 genomic sequencegi|340026733|gb|JF330513.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024