RGD:150418486 Rat Genome Database

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Variant: RGD:150418486 -  Homo sapiens

RGD ID: 150418486
RS ID: rs587680357
ClinVar ID: CV1181925
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126653398  TSPEAR  TSPEAR-AS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 21 45,929,331
GRCh38 21 44,509,448
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001272037.2:c.1363-62G>A
NM_144991.3:c.1567-62G>A
NG_033806.1:g.207131G>A
NC_000021.9:g.44509448C>T
More... 		07/24/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TSPEAR
Accession:NM_144991
Location:INTRON

Gene Symbol:TSPEAR
Accession:NM_001272037
Location:INTRON

Gene Symbol:TSPEAR-AS1
Accession:NR_103707
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001550622 CLINVAR
dbSNP (RS) rs587680357 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126653398 CLINVAR
  TSPEAR CLINVAR
  TSPEAR-AS1 CLINVAR
OMIM 612920 CLINVAR