RGD:8648789 Rat Genome Database

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Variant: RGD:8648789 -  Homo sapiens

RGD ID: 8648789
RS ID: rs199475741
ClinVar ID: CV108950
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NLRP4  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 56,348,091
GRCh38 19 55,836,725
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000019.10:g.55836725T>G
NC_000019.9:g.56348091T>G
NG_052802.1:g.5148T>G
NM_134444.4:c.-275T>G
More... 		5 prime utr variant|utr-5 not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:NLRP4
Accession:NM_134444
Location:5UTRS;EXON

Gene Symbol:NLRP4
Accession:XM_017026345
Location:INTRON

Gene Symbol:NLRP4
Accession:XM_017026344
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000089475 CLINVAR
dbSNP (RS) rs199475741 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene NLRP4 CLINVAR
OMIM 609645 CLINVAR