RGD:13446088 Rat Genome Database

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Variant: RGD:13446088 -  Homo sapiens

RGD ID: 13446088
RS ID: rs374246725
ClinVar ID: CV438477
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLXNA3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 153,694,863
GRCh38 X 154,466,520
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_021298.2:g.13246G>A
NC_000023.11:g.154466520G>A
NC_000023.10:g.153694863G>A
NM_017514.5:c.2936+8G>A
More... 		12/09/2021 intron variant likely benign|uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:PLXNA3
Accession:NM_017514
Location:INTRON

Gene Symbol:PLXNA3
Accession:XM_047442247
Location:INTRON

Gene Symbol:PLXNA3
Accession:XR_430556
Location:INTRON;NON-CODING

Gene Symbol:PLXNA3
Accession:XR_007068193
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000513259 CLINVAR
  RCV003960207 CLINVAR
dbSNP (RS) rs374246725 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLXNA3 CLINVAR
OMIM 300022 CLINVAR