RGD:407486682 Rat Genome Database

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Variant: RGD:407486682 -  Homo sapiens

RGD ID: 407486682
ClinVar ID: CV3462011
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRRC41  RAD54L  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 46,743,518
GRCh38 1 46,277,846
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1414t1:c.1899G>C
NM_006369.5:c.*1019C>G
NM_001370766.1:c.1359G>C
LRG_1414:g.35152G>C
More... 		05/04/2024 3 prime utr variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004669494 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LRRC41 CLINVAR
  RAD54L CLINVAR
OMIM 603615 CLINVAR
  618753 CLINVAR