rs142802838 Rat Genome Database

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Variant: rs142802838 -  Homo sapiens

RGD ID: 150425871
RS ID: rs142802838
ClinVar ID: CV1184025
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AKAP9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 91,661,125
GRCh38 7 92,031,811
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005751.5:c.4338+207C>T
NM_147185.3:c.4338+207C>T
LRG_331:g.95937C>T
NG_011623.1:g.95937C>T
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 Information

Database Acc Id Source(s)
ClinVar RCV001558583 CLINVAR
dbSNP (RS) rs142802838 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene AKAP9 CLINVAR
OMIM 604001 CLINVAR