NM_019109.5(ALG1):c.766G>A (p.Glu256Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004027412.1
Allele description [Variation Report for NM_019109.5(ALG1):c.766G>A (p.Glu256Lys)]
NM_019109.5(ALG1):c.766G>A (p.Glu256Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
JGI_XZG15045.fwd NIH_XGC_tropGas7 Xenopus tropicalis cDNA clone IMAGE:7531099 5'...
JGI_XZG15045.fwd NIH_XGC_tropGas7 Xenopus tropicalis cDNA clone IMAGE:7531099 5', mRNA sequencegi|73751487|gnl|dbEST|31012702|gb|C 39.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024