Annotation Detail
Information
- Associated Genes
- G6PD
- Associated Variants
-
G6PD p.Arg459Leu (p.R459L)
(
ENST00000369620.6,
ENST00000393562.10,
ENST00000393564.7,
ENST00000439227.6,
ENST00000696420.1,
ENST00000696421.1,
ENST00000696429.1,
ENST00000696430.1 )
G6PD p.Arg459Leu (p.R459L) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 ) - Source Database
- ClinVar
- Description
- NM_000402.4(G6PD):c.1466G>T (p.Arg489Leu) AND G6PD CANTON
- ClinVar Allele ID
- 25419
- ClinVar RefSeq Alternation Syntax
- NM_001042351.3:c.1376G>T
- ClinVar RefSeq Alternation Syntax
- NM_001360016.2:c.1376G>T
- ClinVar RefSeq Alternation Syntax
- NM_000402.4:c.1466G>T
- Clinical Significance Description
- other
- Clinical Significance Last Update
- 2017-05-24
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000011104
- Observed Origin Sample
- germline
- Pubmed
- 2263506
- Pubmed
- 6714986
- Pubmed
- 5485383
- Pubmed
- 16832
- Pubmed
- 4283789
- Pubmed
- 1562739
Drugs