NM_000942.5(PPIB):c.459C>T (p.Phe153=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002858485.3
Allele description [Variation Report for NM_000942.5(PPIB):c.459C>T (p.Phe153=)]
NM_000942.5(PPIB):c.459C>T (p.Phe153=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
we38f07.x1 NCI_CGAP_Lu24 Homo sapiens cDNA clone IMAGE:2343397 3', mRNA sequence
we38f07.x1 NCI_CGAP_Lu24 Homo sapiens cDNA clone IMAGE:2343397 3', mRNA sequencegi|4988525|gnl|dbEST|2605163|gb|AI7 .1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024