NM_001374828.1(ARID1B):c.5148C>T (p.Thr1716=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002263422.15
Allele description [Variation Report for NM_001374828.1(ARID1B):c.5148C>T (p.Thr1716=)]
NM_001374828.1(ARID1B):c.5148C>T (p.Thr1716=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
UI-E-DW1-ahc-i-23-0-UI.s1 UI-E-DW1 Homo sapiens cDNA clone UI-E-DW1-ahc-i-23-0-U...
UI-E-DW1-ahc-i-23-0-UI.s1 UI-E-DW1 Homo sapiens cDNA clone UI-E-DW1-ahc-i-23-0-UI 3', mRNA sequencegi|18980070|gnl|dbEST|11251106|gb|B 73.1|Nucleotide
-
BP371008 Sugano cDNA library, testis Homo sapiens cDNA clone TST07614 5', mRNA s...
BP371008 Sugano cDNA library, testis Homo sapiens cDNA clone TST07614 5', mRNA sequencegi|52301276|gnl|dbEST|25637728|dbj| 008.1|Nucleotide
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Last Updated: Oct 8, 2024