rs199476257 Rat Genome Database

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Variant: rs199476257 -  Homo sapiens

RGD ID: 8648885
RS ID: rs199476257
ClinVar ID: CV109046
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NLRP13  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 56,413,595
GRCh38 19 55,902,229
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_176810.2:c.2619-24A>G
NC_000019.10:g.55902229T>C
NC_000019.9:g.56413595T>C
NM_001321057.1:c.2619-24A>G
More... 		intron|intron variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:NLRP13
Accession:NM_001321057
Location:INTRON

Gene Symbol:NLRP13
Accession:NM_176810
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000089571 CLINVAR
dbSNP (RS) rs199476257 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene NLRP13 CLINVAR
OMIM 609660 CLINVAR