NM_203447.3(DOCK8):c.2646G>A (p.Thr882=)Rat Genome Database

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Variant : CV767430 (NM_203447.3(DOCK8):c.2646G>A (p.Thr882=)) Homo sapiens

Symbol: CV767430
Name: NM_203447.3(DOCK8):c.2646G>A (p.Thr882=)
RGD ID: 15122795
Condition: Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive [RCV000940742]
Clinical Significance: benign
Last Evaluated: 09/19/2018
Review Status: criteria provided, single submitter
Related Genes: DOCK8  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NM_001190458.2:c.2442G>A
NM_001193536.1:c.2442G>A
NM_203447.3:c.2646G>A
NG_017007.1:g.172689G>A
NC_000009.12:g.382553G>A
NC_000009.11:g.382553G>A
NP_001177387.1:p.Thr814=
NP_001180465.1:p.Thr814=
NP_982272.2:p.Thr882=
LRG_196t1:c.2646G>A
LRG_196:g.172689G>A
LRG_196p1:p.Thr882=
Position
Human AssemblyChrPosition (strand)Source
GRCh389382,553 - 382,553CLINVAR
GRCh379382,553 - 382,553CLINVAR
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 RCV000940742 CLINVAR
dbSNP (RS) rs373515697 CLINVAR
MedGen C4722305 CLINVAR
NCBI Gene DOCK8 CLINVAR
OMIM 243700 CLINVAR
  611432 CLINVAR