RGD:408376320 Rat Genome Database

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Variant: RGD:408376320 -  Homo sapiens

RGD ID: 408376320
ClinVar ID: CV3513106
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRP2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 206,630,217
GRCh38 2 205,765,493
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_003872.3:c.2327T>C
NM_018534.4:c.2327T>C
NM_201266.2:c.2327T>C
NM_201267.2:c.2327T>C
More... 		12/14/2023 missense variant uncertain significance NRP2-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004749033 CLINVAR
NCBI Gene NRP2 CLINVAR
OMIM 602070 CLINVAR