rs141750225 Rat Genome Database

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Variant: rs141750225 -  Homo sapiens

RGD ID: 150474327
RS ID: rs141750225
ClinVar ID: CV1234432
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: NIPBL  
Reference Nucleotide: A
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 5 36,958,087
GRCh38 5 36,957,985
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_015384.5:c.231-103del
NM_133433.4:c.231-103del
NG_006987.2:g.86119del
NC_000005.10:g.36958001del
More... 		06/03/2021 intron variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001651752 CLINVAR
dbSNP (RS) rs141750225 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NIPBL CLINVAR
OMIM 608667 CLINVAR