RGD:408376509 Rat Genome Database

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Variant: RGD:408376509 -  Homo sapiens

RGD ID: 408376509
ClinVar ID: CV3514423
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRP2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 206,608,068
GRCh38 2 205,743,344
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_003872.3:c.1433T>C
NM_018534.4:c.1433T>C
NM_201264.2:c.1433T>C
NM_201266.2:c.1433T>C
More... 		01/17/2024 missense variant uncertain significance NRP2-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004749224 CLINVAR
NCBI Gene NRP2 CLINVAR
OMIM 602070 CLINVAR