RGD:15131028 Rat Genome Database

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Variant: RGD:15131028 -  Homo sapiens

RGD ID: 15131028
RS ID: rs201608832
ClinVar ID: CV745180
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLXNA3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 153,693,357
GRCh38 X 154,465,014
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_017514.5:c.2044-4G>A
NG_021298.2:g.11740G>A
NC_000023.11:g.154465014G>A
NM_017514.4:c.2044-4G>A
More... 		04/30/2018 intron variant benign 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   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000897702 CLINVAR
  RCV003950498 CLINVAR
dbSNP (RS) rs201608832 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLXNA3 CLINVAR
OMIM 300022 CLINVAR