RGD:150463505 Rat Genome Database

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Variant: RGD:150463505 -  Homo sapiens

RGD ID: 150463505
RS ID: rs41277471
ClinVar ID: CV1253813
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127896415  SREBF2-AS1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 22 42,229,092
GRCh38 22 41,833,088
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_068430.1:g.37410G>C
NC_000022.11:g.41833088G>C
NC_000022.10:g.42229092G>C
NR_157279.2:n.1116C>G
 05/17/2021 non-coding transcript variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SREBF2-AS1
Accession:NR_157279
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001669855 CLINVAR
dbSNP (RS) rs41277471 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SREBF2 CLINVAR
  SREBF2-AS1 CLINVAR
OMIM 600481 CLINVAR