RGD:150474845 Rat Genome Database

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Variant: RGD:150474845 -  Homo sapiens

RGD ID: 150474845
RS ID: rs748843981
ClinVar ID: CV1263418
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TPSAB1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 1,290,835
GRCh38 16 1,240,834
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003294.4:c.1-105C>A
NC_000016.10:g.1240834C>A
NC_000016.9:g.1290835C>A
 05/15/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TPSAB1
Accession:NM_003294
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001684941 CLINVAR
dbSNP (RS) rs748843981 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TPSAB1 CLINVAR
OMIM 191080 CLINVAR