NM_000074.3(CD40LG):c.770G>A (p.Gly257Asp)Rat Genome Database

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Variant : CV951625 (NM_000074.3(CD40LG):c.770G>A (p.Gly257Asp)) Homo sapiens

Symbol: CV951625
Name: NM_000074.3(CD40LG):c.770G>A (p.Gly257Asp)
RGD ID: 38487476
Condition: Hyper-IgM syndrome type 1 [RCV001237589]
Clinical Significance: pathogenic
Last Evaluated: 10/19/2019
Review Status: criteria provided, single submitter
Related Genes: CD40LG  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): LRG_141t1:c.770G>A
NM_000074.3:c.770G>A
LRG_141:g.16223G>A
NG_007280.1:g.16223G>A
NC_000023.11:g.136659399G>A
NC_000023.10:g.135741558G>A
NM_000074.2:c.770G>A
NP_000065.1:p.Gly257Asp
Position
Human AssemblyChrPosition (strand)Source
GRCh38X136,659,399 - 136,659,399CLINVAR
GRCh37X135,741,558 - 135,741,558CLINVAR
Cytogenetic MapXXq26.3CLINVAR
Trait Synonyms: Hyper IgM immunodeficiency, X-linked; Hyper-IgM Immunodeficiency Syndrome, Type 1; IMMUNODEFICIENCY 3; Immunodeficiency with hyper IgM type 1; X-linked hyper-IgM syndrome



Disease Annotations     Click to see Annotation Detail View

Additional References at PubMed
PMID:8889581   PMID:10366125   PMID:20981468   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001237589 CLINVAR
MedGen C0398689 CLINVAR
NCBI Gene CD40LG CLINVAR
OMIM 300386 CLINVAR
  308230 CLINVAR