RGD:13476281 Rat Genome Database

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Variant: RGD:13476281 -  Homo sapiens

RGD ID: 13476281
RS ID: rs755410266
ClinVar ID: CV460988
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANO5  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 22,296,109
GRCh38 11 22,274,563
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.10:g.22274563C>T
NC_000011.9:g.22296109C>T
LRG_868t1:c.2236-6C>T
LRG_868:g.86388C>T
More... 		06/26/2018 intron variant likely benign Autosomal recessive limb-girdle muscular dystrophy type 2L; GNATHODIAPHYSEAL SCLEROSIS; Levin syndrome 2; Limb-girdle muscular dystrophy, type 2L; MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 12; Osteogenesis imperfecta Levin type; Osteogenesis imperfecta with unusual skeletal lesions
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ANO5
Accession:XM_011519949
Location:INTRON

Gene Symbol:ANO5
Accession:NM_001142649
Location:INTRON

Gene Symbol:ANO5
Accession:NM_001410963
Location:INTRON

Gene Symbol:ANO5
Accession:NM_213599
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ANO5
Accession:XM_047426522
Location:INTRON

Gene Symbol:ANO5
Accession:XM_005252822
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ANO5
Accession:NM_001410964
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002526160 CLINVAR
dbSNP (RS) rs755410266 CLINVAR
MedGen C1833736 CLINVAR
NCBI Gene ANO5 CLINVAR
OMIM 166260 CLINVAR
  608662 CLINVAR
  611307 CLINVAR