RGD:152044009 Rat Genome Database

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Variant: RGD:152044009 -  Homo sapiens

RGD ID: 152044009
RS ID: rs569031640
ClinVar ID: CV1584132
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAH11  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 21,757,560
GRCh38 7 21,717,942
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001277115.2:c.7134+17G>A
NG_012886.2:g.179728G>A
NC_000007.14:g.21717942G>A
NC_000007.13:g.21757560G>A
 07/08/2021 intron variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DNAH11
Accession:NM_001277115
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002071382 CLINVAR
dbSNP (RS) rs569031640 CLINVAR
MedGen C0008780 CLINVAR
NCBI Gene DNAH11 CLINVAR
OMIM 603339 CLINVAR