NM_007198.4(PLPBP):c.132G>T (p.Ala44=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002604183.3
Allele description [Variation Report for NM_007198.4(PLPBP):c.132G>T (p.Ala44=)]
NM_007198.4(PLPBP):c.132G>T (p.Ala44=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
602043351F1 NCI_CGAP_Brn67 Homo sapiens cDNA clone IMAGE:4180981 5', mRNA sequen...
602043351F1 NCI_CGAP_Brn67 Homo sapiens cDNA clone IMAGE:4180981 5', mRNA sequencegi|11616251|gnl|dbEST|6965285|gb|BF 8.1|Nucleotide
-
UI-E-CI1-afp-f-12-0-UI.s1 UI-E-CI1 Homo sapiens cDNA clone UI-E-CI1-afp-f-12-0-U...
UI-E-CI1-afp-f-12-0-UI.s1 UI-E-CI1 Homo sapiens cDNA clone UI-E-CI1-afp-f-12-0-UI 3', mRNA sequencegi|23654536|gnl|dbEST|14195139|gb|B 42.1|Nucleotide
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Last Updated: Sep 29, 2024