Annotation Detail

Information
Associated Genes
G6PD
Associated Variants
G6PD p.Asp181Val (p.D181V) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 )
G6PD p.Asn126Asp (p.N126D) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 )
G6PD p.Asp181Val (p.D181V) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 )
G6PD p.Asn126Asp (p.N126D) ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 )
Source Database
ClinVar
Description
NM_001042351.1(G6PD):c.[376A>G;542A>T] AND G6PD SANTAMARIA
ClinVar Allele ID
25399
ClinVar Allele ID
25421
ClinVar RefSeq Alternation Syntax
NM_001360016.2:c.542A>T
ClinVar RefSeq Alternation Syntax
NM_000402.4:c.466A>G
ClinVar RefSeq Alternation Syntax
NM_000402.4:c.632A>T
ClinVar RefSeq Alternation Syntax
NM_001042351.3:c.542A>T
ClinVar RefSeq Alternation Syntax
NM_001042351.3:c.376A>G
ClinVar RefSeq Alternation Syntax
NM_001360016.2:c.376A>G
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/RCV000011109
Observed Origin Sample
germline
Pubmed
6433630
Pubmed
1978554
Drugs