NM_000528.4(MAN2B1):c.1043G>A (p.Ser348Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003295396.2
Allele description [Variation Report for NM_000528.4(MAN2B1):c.1043G>A (p.Ser348Asn)]
NM_000528.4(MAN2B1):c.1043G>A (p.Ser348Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homologene neighbors for GEO Profiles (Select 132507440) (0)
GEO Profiles
-
Homologene neighbors for GEO Profiles (Select 118872820) (0)
GEO Profiles
-
Homologene neighbors for GEO Profiles (Select 72502890) (0)
GEO Profiles
-
Homologene neighbors for GEO Profiles (Select 72494923) (0)
GEO Profiles
-
Profile neighbors for GEO Profiles (Select 72502890) (200)
GEO Profiles
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024