NM_000228.3(LAMB3):c.1597+17T>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 8, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003545294.2
Allele description [Variation Report for NM_000228.3(LAMB3):c.1597+17T>A]
NM_000228.3(LAMB3):c.1597+17T>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens prolylcarboxypeptidase (PRCP), transcript variant 2, mRNA
Homo sapiens prolylcarboxypeptidase (PRCP), transcript variant 2, mRNAgi|1889462748|ref|NM_199418.4|Nucleotide
-
cytochrome b (mitochondrion) [Acosmetura nigrogeniculata]
cytochrome b (mitochondrion) [Acosmetura nigrogeniculata]gi|1778128417|ref|YP_009711023.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024