RGD:407510214 Rat Genome Database

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Variant: RGD:407510214 -  Homo sapiens

RGD ID: 407510214
ClinVar ID: CV3432504
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FNDC3A  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 13 49,781,316
GRCh38 13 49,207,180
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014923.5:c.3214C>G
NM_001079673.2:c.3382C>G
NM_001278438.2:c.3382C>G
NC_000013.11:g.49207180C>G
More... 		05/13/2024 missense variant likely benign AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004626024 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene FNDC3A CLINVAR
OMIM 615794 CLINVAR