NC_000016.10:g.8797723G>A AND PMM2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003894510.1
Allele description [Variation Report for NC_000016.10:g.8797723G>A]
NC_000016.10:g.8797723G>A
Condition(s)
- Name:
- PMM2-related disorder
- Synonyms:
- PMM2-related condition
- Identifiers:
-
Imaging practice and involvement of the neurosurgical department - Head Injury
Imaging practice and involvement of the neurosurgical department - Head Injury
-
K-EST0100384 S11SNU1 Homo sapiens cDNA clone S11SNU1-39-H05 5', mRNA sequence
K-EST0100384 S11SNU1 Homo sapiens cDNA clone S11SNU1-39-H05 5', mRNA sequencegi|19184114|gnl|dbEST|11427779|gb|B 05.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 19, 2024