RGD:28883855 Rat Genome Database

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Variant: RGD:28883855 -  Homo sapiens

RGD ID: 28883855
RS ID: rs921086000
ClinVar ID: CV902892
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: G6PD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 153,759,616
GRCh38 X 154,531,401
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001360016.2:c.*599C>T
NG_009015.2:g.21172C>T
NM_001042351.1:c.*599C>T
NM_000402.4:c.*599C>T
More... 		01/12/2018 3 prime utr variant uncertain significance G6PD A-; Glucose 6 phosphate dehydrogenase deficiency
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:G6PD
Accession:NM_001042351
Location:3UTRS;EXON

Gene Symbol:G6PD
Accession:NM_000402
Location:3UTRS;EXON

Gene Symbol:G6PD
Accession:NM_001360016
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001168331 CLINVAR
dbSNP (RS) rs921086000 CLINVAR
MedGen C2939465 CLINVAR
NCBI Gene G6PD CLINVAR
OMIM 305900 CLINVAR