NM_019043.4(APBB1IP):c.1657T>A (p.Phe553Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004291891.1
Allele description [Variation Report for NM_019043.4(APBB1IP):c.1657T>A (p.Phe553Ile)]
NM_019043.4(APBB1IP):c.1657T>A (p.Phe553Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens BCL2-associated X protein, mRNA (cDNA clone MGC:20956 IMAGE:4578562...
Homo sapiens BCL2-associated X protein, mRNA (cDNA clone MGC:20956 IMAGE:4578562), complete cdsgi|33991524|gb|BC014175.2|Nucleotide
-
AGENCOURT_7945613 NIH_MGC_72 Homo sapiens cDNA clone IMAGE:6149935 5', mRNA sequ...
AGENCOURT_7945613 NIH_MGC_72 Homo sapiens cDNA clone IMAGE:6149935 5', mRNA sequencegi|22701971|gnl|dbEST|13464857|gb|B 87.1|Nucleotide
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Last Updated: Oct 13, 2024