NM_000814.6(GABRB3):c.1113G>A (p.Ser371=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 25, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000601997.1
Allele description [Variation Report for NM_000814.6(GABRB3):c.1113G>A (p.Ser371=)]
NM_000814.6(GABRB3):c.1113G>A (p.Ser371=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
300200 (1)
OMIM
-
Homo sapiens cDNA FLJ77100 complete cds
Homo sapiens cDNA FLJ77100 complete cdsgi|158255263|dbj|AK290914.1|Nucleotide
-
OMIM Links for Gene (Select 1371) (3)
OMIM
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See more...Assertion and evidence details
Last Updated: May 26, 2024