RGD:407485741 Rat Genome Database

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Variant: RGD:407485741 -  Homo sapiens

RGD ID: 407485741
ClinVar ID: CV3472207
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RALGAPB  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 37,202,794
GRCh38 20 38,574,151
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001282918.2:c.4135T>G
NM_001282917.2:c.4144T>G
NM_020336.4:c.4144T>G
NC_000020.11:g.38574151T>G
More... 		05/14/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004665370 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RALGAPB CLINVAR
OMIM 618833 CLINVAR