RGD:28886460 Rat Genome Database

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Variant: RGD:28886460 -  Homo sapiens

RGD ID: 28886460
RS ID: rs938857639
ClinVar ID: CV902896
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: G6PD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 153,760,140
GRCh38 X 154,531,925
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000402.4:c.*75C>T
NM_001042351.3:c.*75C>T
NG_009015.2:g.20648C>T
NM_001042351.1:c.*75C>T
More... 		01/13/2018 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_001360016
Location:3UTRS;EXON

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

Gene Symbol:G6PD
Accession:NM_001042351
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001169070 CLINVAR
dbSNP (RS) rs938857639 CLINVAR
MedGen C2939465 CLINVAR
NCBI Gene G6PD CLINVAR
OMIM 305900 CLINVAR