NM_014795.4(ZEB2):c.3342G>C (p.Gln1114His) AND Mowat-Wilson syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003613340.2
Allele description [Variation Report for NM_014795.4(ZEB2):c.3342G>C (p.Gln1114His)]
NM_014795.4(ZEB2):c.3342G>C (p.Gln1114His)
Condition(s)
-
Tssr59407 AND (alive[prop]) (0)
Gene
-
LOC107984902 [Homo sapiens]
LOC107984902 [Homo sapiens]Gene ID:107984902Gene
-
IGHV3-6 immunoglobulin heavy variable 3-6 (pseudogene) [Homo sapiens]
IGHV3-6 immunoglobulin heavy variable 3-6 (pseudogene) [Homo sapiens]Gene ID:28453Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024