NM_203447.4(DOCK8):c.4276A>G (p.Ser1426Gly)Rat Genome Database

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Variant : CV946650 (NM_203447.4(DOCK8):c.4276A>G (p.Ser1426Gly)) Homo sapiens

Symbol: CV946650
Name: NM_203447.4(DOCK8):c.4276A>G (p.Ser1426Gly)
RGD ID: 38486659
Condition: Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive [RCV001237258]
Clinical Significance: uncertain significance
Last Evaluated: 08/26/2019
Review Status: criteria provided, single submitter
Related Genes: DOCK8  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): LRG_196t1:c.4276A>G
NM_001190458.2:c.3976A>G
NM_001193536.1:c.4072A>G
NM_203447.4:c.4276A>G
LRG_196:g.217055A>G
NG_017007.1:g.217055A>G
NC_000009.12:g.426919A>G
NC_000009.11:g.426919A>G
NM_203447.3:c.4276A>G
NP_001177387.1:p.Ser1326Gly
NP_001180465.1:p.Ser1358Gly
NP_982272.2:p.Ser1426Gly
Position
Human AssemblyChrPosition (strand)Source
GRCh389426,919 - 426,919CLINVAR
GRCh379426,919 - 426,919CLINVAR
Cytogenetic Map99p24.3CLINVAR
Trait Synonyms: AR hyperimmunoglobulin E syndrome; HIES autosomal recessive; Hyper Ig E syndrome, autosomal recessive; HYPER-IgE RECURRENT INFECTION SYNDROME 2, AUTOSOMAL RECESSIVE



Disease Annotations     Click to see Annotation Detail View

Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001237258 CLINVAR
MedGen C4722305 CLINVAR
NCBI Gene DOCK8 CLINVAR
OMIM 243700 CLINVAR
  611432 CLINVAR