RGD:12889925 Rat Genome Database

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Variant: RGD:12889925 -  Homo sapiens

RGD ID: 12889925
RS ID: rs72657314
ClinVar ID: CV395559
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAH11  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 21,658,711
GRCh38 7 21,619,093
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012886.2:g.80879C>G
NC_000007.14:g.21619093C>G
NC_000007.13:g.21658711C>G
NM_001277115.2:c.4255-7C>G
More... 		11/21/2018 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 RCV000473651 CLINVAR
dbSNP (RS) rs72657314 CLINVAR
MedGen C0008780 CLINVAR
NCBI Gene DNAH11 CLINVAR
OMIM 603339 CLINVAR