RGD:408384564 Rat Genome Database

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Variant: RGD:408384564 -  Homo sapiens

RGD ID: 408384564
ClinVar ID: CV3504327
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NCF4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 37,273,756
GRCh38 22 36,877,714
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_159t1:c.*109C>T
NM_013416.4:c.*109C>T
NM_000631.5:c.911C>T
LRG_159:g.21727C>T
More... 		07/16/2024 3 prime utr variant uncertain significance NCF4-related condition

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004731919 CLINVAR
NCBI Gene NCF4 CLINVAR
OMIM 601488 CLINVAR