NM_014847.4(UBAP2L):c.655G>A (p.Gly219Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004170713.1
Allele description [Variation Report for NM_014847.4(UBAP2L):c.655G>A (p.Gly219Ser)]
NM_014847.4(UBAP2L):c.655G>A (p.Gly219Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
SCHIP1 schwannomin interacting protein 1 [Homo sapiens]
SCHIP1 schwannomin interacting protein 1 [Homo sapiens]Gene ID:29970Gene
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Last Updated: May 26, 2024