RGD:150475531 Rat Genome Database

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Variant: RGD:150475531 -  Homo sapiens

RGD ID: 150475531
RS ID: rs78026972
ClinVar ID: CV1279078
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TSPEAR  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 21 45,942,107
GRCh38 21 44,522,224
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.1133-112C>T
NM_144991.3:c.1337-112C>T
NG_033806.1:g.194355C>T
NC_000021.9:g.44522224G>A
More... 		12/17/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TSPEAR
Accession:NM_001272037
Location:INTRON

Gene Symbol:TSPEAR
Accession:NM_144991
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001713854 CLINVAR
dbSNP (RS) rs78026972 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TSPEAR CLINVAR
OMIM 612920 CLINVAR