GRCh38/hg38 1p36.33-36.32(chr1:911300-2963389)x1 AND See cases
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Dec 22, 2010
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000142754.5
Allele description [Variation Report for GRCh38/hg38 1p36.33-36.32(chr1:911300-2963389)x1]
GRCh38/hg38 1p36.33-36.32(chr1:911300-2963389)x1
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
LOC129929165 [Homo sapiens]
LOC129929165 [Homo sapiens]Gene ID:129929165Gene
-
LOC129929092 [Homo sapiens]
LOC129929092 [Homo sapiens]Gene ID:129929092Gene
-
LOC129929170 [Homo sapiens]
LOC129929170 [Homo sapiens]Gene ID:129929170Gene
-
LOC129929133 [Homo sapiens]
LOC129929133 [Homo sapiens]Gene ID:129929133Gene
-
ACAP3 ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 [Homo sapiens]
ACAP3 ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 [Homo sapiens]Gene ID:116983Gene
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See more...Assertion and evidence details
Last Updated: May 7, 2024