rs1304799923 Rat Genome Database

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Variant: rs1304799923 -  Homo sapiens

RGD ID: 152076420
RS ID: rs1304799923
ClinVar ID: CV1542893
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AKAP9  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 91,706,159
GRCh38 7 92,076,845
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001379277.1:c.1258-10G>A
NM_147185.3:c.6589-10G>A
NM_005751.5:c.6613-10G>A
LRG_331:g.140971G>A
More... 		09/06/2021 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:AKAP9
Accession:NM_005751
Location:INTRON

Gene Symbol:AKAP9
Accession:NM_147185
Location:INTRON

Gene Symbol:AKAP9
Accession:NM_001379277
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002130279 CLINVAR
dbSNP (RS) rs1304799923 CLINVAR
MedGen C0023976 CLINVAR
NCBI Gene AKAP9 CLINVAR
OMIM 604001 CLINVAR
SNOMED CT 9651007 CLINVAR