RGD:408377325 Rat Genome Database

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Variant: RGD:408377325 -  Homo sapiens

RGD ID: 408377325
ClinVar ID: CV3508544
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRP2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 206,659,534
GRCh38 2 205,794,810
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NP_958436.1:p.Pro828Ala
NP_003863.2:p.Pro845Ala
NP_957718.1:p.Pro850Ala
NM_201279.2:c.2482C>G
More... 		11/11/2023 missense variant uncertain significance NRP2-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004750678 CLINVAR
NCBI Gene NRP2 CLINVAR
OMIM 602070 CLINVAR