NM_000834.5(GRIN2B):c.72C>T (p.Ser24=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003118074.5
Allele description [Variation Report for NM_000834.5(GRIN2B):c.72C>T (p.Ser24=)]
NM_000834.5(GRIN2B):c.72C>T (p.Ser24=)
Condition(s)
-
golgin subfamily A member 7 isoform a [Homo sapiens]
golgin subfamily A member 7 isoform a [Homo sapiens]gi|50541946|ref|NP_001002296.1|Protein
-
T-cell leukemia translocation-altered gene protein [Homo sapiens]
T-cell leukemia translocation-altered gene protein [Homo sapiens]gi|11560141|ref|NP_071503.1|Protein
-
RecName: Full=Major facilitator superfamily domain-containing protein 8
RecName: Full=Major facilitator superfamily domain-containing protein 8gi|81896075|sp|Q8BH31.1|MFSD8_MOUSEProtein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024