NM_001113491.2(SEPTIN9):c.320G>A (p.Arg107His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003866748.1
Allele description [Variation Report for NM_001113491.2(SEPTIN9):c.320G>A (p.Arg107His)]
NM_001113491.2(SEPTIN9):c.320G>A (p.Arg107His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens solute carrier family 16 member 3 (SLC16A3), transcript variant 2, ...
Homo sapiens solute carrier family 16 member 3 (SLC16A3), transcript variant 2, mRNAgi|1890259789|ref|NM_001042422.3|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Mar 5, 2024