RGD:152095692 Rat Genome Database

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Variant: RGD:152095692 -  Homo sapiens

RGD ID: 152095692
RS ID: rs1785740654
ClinVar ID: CV1653185
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAH11  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 21,778,491
GRCh38 7 21,738,873
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.7811+7A>T
NG_012886.2:g.200659A>T
NC_000007.14:g.21738873A>T
NC_000007.13:g.21778491A>T
 10/14/2021 intron variant likely 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 RCV002094804 CLINVAR
dbSNP (RS) rs1785740654 CLINVAR
MedGen C0008780 CLINVAR
NCBI Gene DNAH11 CLINVAR
OMIM 603339 CLINVAR