RGD:150495570 Rat Genome Database

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Variant: RGD:150495570 -  Homo sapiens

RGD ID: 150495570
RS ID: rs79462002
ClinVar ID: CV1282987
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATL3  LOC126861231  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 63,399,175
GRCh38 11 63,631,703
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001290048.2:c.1054-232G>A
NM_015459.5:c.1108-232G>A
NG_033985.1:g.45272G>A
NC_000011.10:g.63631703C>T
More... 		04/02/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ATL3
Accession:NM_015459
Location:INTRON

Gene Symbol:ATL3
Accession:XM_006718493
Location:INTRON

Gene Symbol:ATL3
Accession:NM_001290048
Location:INTRON

Gene Symbol:ATL3
Accession:XM_047426725
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001717409 CLINVAR
dbSNP (RS) rs79462002 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ATL3 CLINVAR
  LOC126861231 CLINVAR
OMIM 609369 CLINVAR