NM_203447.4(DOCK8):c.313C>G (p.Pro105Ala)Rat Genome Database

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Variant : CV925557 (NM_203447.4(DOCK8):c.313C>G (p.Pro105Ala)) Homo sapiens

Symbol: CV925557
Name: NM_203447.4(DOCK8):c.313C>G (p.Pro105Ala)
RGD ID: 38481323
Condition: Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive [RCV001217956]
Clinical Significance: uncertain significance
Last Evaluated: 04/02/2019
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.313C>G
NM_001190458.2:c.109C>G
NM_001193536.1:c.109C>G
NM_203447.4:c.313C>G
LRG_196:g.76753C>G
NG_017007.1:g.76753C>G
NC_000009.12:g.286617C>G
NC_000009.11:g.286617C>G
NM_203447.3:c.313C>G
NP_982272.2:p.Pro105Ala
NP_001177387.1:p.Pro37Ala
NP_001180465.1:p.Pro37Ala
Position
Human AssemblyChrPosition (strand)Source
GRCh389286,617 - 286,617CLINVAR
GRCh379286,617 - 286,617CLINVAR
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 RCV001217956 CLINVAR
MedGen C4722305 CLINVAR
NCBI Gene DOCK8 CLINVAR
OMIM 243700 CLINVAR
  611432 CLINVAR