RGD:408376776 Rat Genome Database

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Variant: RGD:408376776 -  Homo sapiens

RGD ID: 408376776
ClinVar ID: CV3516412
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127275595  NRP2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 206,614,570
GRCh38 2 205,749,846
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_003872.3:c.1903+5G>A
NM_018534.4:c.1903+5G>A
NM_201266.2:c.1903+5G>A
NM_201267.2:c.1903+5G>A
More... 		06/29/2023 intron variant likely benign NRP2-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004749469 CLINVAR
NCBI Gene NRP2 CLINVAR
OMIM 602070 CLINVAR