RGD:597785128 Rat Genome Database

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Variant: RGD:597785128 -  Homo sapiens

RGD ID: 597785128
ClinVar ID: CV3586008
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127814297  LOC129994940  RBM27  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 145,583,341
GRCh38 5 146,203,778
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001414499.1:c.13G>A
NM_018989.2:c.13G>A
NG_174386.1:g.218G>A
NC_000005.10:g.146203778G>A
More... 		09/02/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004854651 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LOC127814297 CLINVAR
  LOC129994940 CLINVAR
  RBM27 CLINVAR
OMIM 620082 CLINVAR