NM_000293.3(PHKB):c.2977C>A (p.Pro993Thr) AND Glycogen storage disease IXb
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002862932.3
Allele description [Variation Report for NM_000293.3(PHKB):c.2977C>A (p.Pro993Thr)]
NM_000293.3(PHKB):c.2977C>A (p.Pro993Thr)
Condition(s)
-
Homo sapiens solute carrier family 2 (facilitated glucose transporter), member 1...
Homo sapiens solute carrier family 2 (facilitated glucose transporter), member 10, mRNA (cDNA clone MGC:126706 IMAGE:8069163), complete cdsgi|75516677|gb|BC101657.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024