NM_033109.5(PNPT1):c.2149-14A>T AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002158899.5
Allele description [Variation Report for NM_033109.5(PNPT1):c.2149-14A>T]
NM_033109.5(PNPT1):c.2149-14A>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
tu22b11.x1 NCI_CGAP_Pr28 Homo sapiens cDNA clone IMAGE:2251773 3', mRNA sequence
tu22b11.x1 NCI_CGAP_Pr28 Homo sapiens cDNA clone IMAGE:2251773 3', mRNA sequencegi|4762243|gnl|dbEST|2487319|gb|AI6 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Mar 5, 2024