NM_005862.3(STAG1):c.3033T>A (p.Ser1011=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003726003.2
Allele description [Variation Report for NM_005862.3(STAG1):c.3033T>A (p.Ser1011=)]
NM_005862.3(STAG1):c.3033T>A (p.Ser1011=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens chromosome 8, clone RP11-1077K19, complete sequence
Homo sapiens chromosome 8, clone RP11-1077K19, complete sequencegi|21539715|gnl|WIBR|L22043|gb|AC10 5|Nucleotide
-
JM332
JM332biosample
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024