RGD:408387311 Rat Genome Database

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Variant: RGD:408387311 -  Homo sapiens

RGD ID: 408387311
ClinVar ID: CV3524497
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAH14  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 225,239,188
GRCh38 1 225,051,486
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001367479.1:c.2115G>A
NG_053088.1:g.128065G>A
NC_000001.11:g.225051486G>A
NC_000001.10:g.225239188G>A
More... 		12/07/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004768371 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAH14 CLINVAR
OMIM 603341 CLINVAR