NM_001379500.1(COL18A1):c.2928C>T (p.Pro976=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002099759.5
Allele description [Variation Report for NM_001379500.1(COL18A1):c.2928C>T (p.Pro976=)]
NM_001379500.1(COL18A1):c.2928C>T (p.Pro976=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens SEC3-like 1 (S. cerevisiae) (SEC3L1), transcript variant 2, mRNA
Homo sapiens SEC3-like 1 (S. cerevisiae) (SEC3L1), transcript variant 2, mRNAgi|30410715|ref|NM_178237.1|Nucleotide
-
pro-neuregulin-1, membrane-bound isoform isoform GGF2 precursor [Homo sapiens]
pro-neuregulin-1, membrane-bound isoform isoform GGF2 precursor [Homo sapiens]gi|116006967|ref|NP_039256.2|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Feb 28, 2024