RGD:150464151 Rat Genome Database

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Variant: RGD:150464151 -  Homo sapiens

RGD ID: 150464151
RS ID: rs8127026
ClinVar ID: CV1273258
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124905038  TSPEAR  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 21 45,951,086
GRCh38 21 44,531,203
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.339-70T>C
NM_144991.3:c.543-70T>C
NG_033806.1:g.185376T>C
NC_000021.9:g.44531203A>G
More... 		06/21/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LOC124905038
Accession:XR_007067905
Location:EXON;NON-CODING

Gene Symbol:TSPEAR
Accession:NM_144991
Location:INTRON

Gene Symbol:TSPEAR
Accession:NM_001272037
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001694015 CLINVAR
dbSNP (RS) rs8127026 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TSPEAR CLINVAR
OMIM 612920 CLINVAR