NM_005097.4(LGI1):c.1062T>G (p.Ala354=) AND Autosomal dominant epilepsy with auditory features
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002072140.5
Allele description [Variation Report for NM_005097.4(LGI1):c.1062T>G (p.Ala354=)]
NM_005097.4(LGI1):c.1062T>G (p.Ala354=)
Condition(s)
- Name:
- Autosomal dominant epilepsy with auditory features
- Identifiers:
- MONDO: MONDO:0010898; MedGen: C1838062
-
4UJP_4UJRQ (0)
Protein
-
Aldehyde:ferredoxin oxidoreductase [Clostridium acetobutylicum EA 2018]
Aldehyde:ferredoxin oxidoreductase [Clostridium acetobutylicum EA 2018]gi|325509434|gnl|SIPPE|CEA_G2033|gb 1070.1|Protein
-
zwf [Zymomonas mobilis subsp. mobilis ZM4 = ATCC 31821]
zwf [Zymomonas mobilis subsp. mobilis ZM4 = ATCC 31821]Gene ID:58026216Gene
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See more...Assertion and evidence details
Last Updated: May 19, 2024