RGD:408376345 Rat Genome Database

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Variant: RGD:408376345 -  Homo sapiens

RGD ID: 408376345
ClinVar ID: CV3513276
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRP2  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 206,587,321
GRCh38 2 205,722,597
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_003872.3:c.553A>T
NM_018534.4:c.553A>T
NM_201264.2:c.553A>T
NM_201266.2:c.553A>T
More... 		12/05/2023 missense variant uncertain significance NRP2-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004749061 CLINVAR
NCBI Gene NRP2 CLINVAR
OMIM 602070 CLINVAR