NM_005861.4(STUB1):c.714G>A (p.Glu238=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003545184.2
Allele description [Variation Report for NM_005861.4(STUB1):c.714G>A (p.Glu238=)]
NM_005861.4(STUB1):c.714G>A (p.Glu238=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens small ubiquitin like modifier 1 (SUMO1), transcript variant 3, mRNA
Homo sapiens small ubiquitin like modifier 1 (SUMO1), transcript variant 3, mRNAgi|1701108504|ref|NM_001005782.2|Nucleotide
-
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 [Hom...
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 [Homo sapiens]gi|119571608|gb|EAW51223.1||gnl|WGS |hCP43521Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024