NM_007357.3(COG2):c.1709A>G (p.Lys570Arg) AND Congenital disorder of glycosylation, type IIq
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 4, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001202815.4
Allele description [Variation Report for NM_007357.3(COG2):c.1709A>G (p.Lys570Arg)]
NM_007357.3(COG2):c.1709A>G (p.Lys570Arg)
Condition(s)
-
copper-transporting ATPase 2 isoform c [Homo sapiens]
copper-transporting ATPase 2 isoform c [Homo sapiens]gi|342187274|ref|NP_001230111.1|Protein
-
F-box/kelch-repeat protein At1g23390-like isoform X2 [Cucurbita moschata]
F-box/kelch-repeat protein At1g23390-like isoform X2 [Cucurbita moschata]gi|1279817386|ref|XP_022962361.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024