NM_007327.4(GRIN1):c.2511C>T (p.Tyr837=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002318145.9
Allele description [Variation Report for NM_007327.4(GRIN1):c.2511C>T (p.Tyr837=)]
NM_007327.4(GRIN1):c.2511C>T (p.Tyr837=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Halomonas sp. 146Z8-2 16S ribosomal RNA gene, partial sequence
Halomonas sp. 146Z8-2 16S ribosomal RNA gene, partial sequencegi|400296058|gb|JX310271.1|Nucleotide
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Last Updated: Oct 26, 2024