RGD:8648704 Rat Genome Database

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Variant: RGD:8648704 -  Homo sapiens

RGD ID: 8648704
RS ID: rs199476032
ClinVar ID: CV108865
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NLRX1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 119,042,066
GRCh38 11 119,171,357
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.10:g.119171357A>G
NC_000011.9:g.119042066A>G
NM_024618.2:c.-47A>G
NG_047185.1:g.8024A>G
More... 		5 prime utr variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:NLRX1
Accession:XM_011542980
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:NM_001282358
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:XM_047427586
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:NM_001282144
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:XM_006718904
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:NM_001282143
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:XM_047427587
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:NM_170722
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:NM_024618
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:XM_005271669
Location:5UTRS;EXON

Gene Symbol:NLRX1
Accession:XM_047427589
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000089390 CLINVAR
dbSNP (RS) rs199476032 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene NLRX1 CLINVAR
OMIM 611947 CLINVAR