RGD:408377260 Rat Genome Database

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Variant: RGD:408377260 -  Homo sapiens

RGD ID: 408377260
ClinVar ID: CV3507728
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRP2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 206,587,353
GRCh38 2 205,722,629
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NP_003863.2:p.Asp195=
NM_003872.3:c.585C>T
NM_018534.4:c.585C>T
NC_000002.12:g.205722629C>T
More... 		09/07/2023 synonymous variant likely benign NRP2-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004750572 CLINVAR
NCBI Gene NRP2 CLINVAR
OMIM 602070 CLINVAR