RGD:407477254 Rat Genome Database

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Variant: RGD:407477254 -  Homo sapiens

RGD ID: 407477254
ClinVar ID: CV3465912
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRK  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 105,153,038
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_198465.4:c.1405C>G
NG_021425.2:g.91504C>G
NC_000023.11:g.105909046C>G
NC_000023.10:g.105153038C>G
More... 		04/15/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004638710 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene NRK CLINVAR
OMIM 300791 CLINVAR