RGD:13474197 Rat Genome Database

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Variant: RGD:13474197 -  Homo sapiens

RGD ID: 13474197
RS ID: rs1557236015
ClinVar ID: CV446588
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IKBKG  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 153,784,379
GRCh38 X 154,556,164
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009896.1:g.18921G>A
NC_000023.10:g.153784379G>A
NM_003639.3:c.188-1G>A
NM_003639.4:c.188-1G>A
More... 		12/18/2015 splice acceptor variant pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:IKBKG
Accession:NM_001099856
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001321396
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_003639
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001321397
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001145255
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001377314
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001377315
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001099857
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001377313
Location:INTRON

Gene Symbol:IKBKG
Accession:NM_001377312
Location:INTRON

Gene Symbol:IKBKG
Accession:NR_165197
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000519580 CLINVAR
dbSNP (RS) rs1557236015 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene IKBKG CLINVAR
OMIM 300248 CLINVAR