RGD:155716025 Rat Genome Database

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Variant: RGD:155716025 -  Homo sapiens

RGD ID: 155716025
ClinVar ID: CV1812450
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AKAP9  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 91,708,390
GRCh38 7 92,079,076
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.1591-3T>C
NM_147185.3:c.6922-3T>C
NM_005751.5:c.6946-3T>C
LRG_331:g.143202T>C
More... 		09/03/2019 intron variant uncertain significance

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 Information

Database Acc Id Source(s)
ClinVar RCV002362443 CLINVAR
MedGen CN230736 CLINVAR
NCBI Gene AKAP9 CLINVAR
OMIM 604001 CLINVAR