rs143403732 Rat Genome Database

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Variant: rs143403732 -  Homo sapiens

RGD ID: 150336071
RS ID: rs143403732
ClinVar ID: CV1171776
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AKAP9  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 91,643,758
GRCh38 7 92,014,444
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.92014444G>A
NC_000007.13:g.91643758G>A
NM_005751.5:c.3612+116G>A
NM_147185.3:c.3612+116G>A
More... 		07/11/2018 intron variant likely benign none provided

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:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001540827 CLINVAR
dbSNP (RS) rs143403732 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene AKAP9 CLINVAR
OMIM 604001 CLINVAR