RGD:151734831 Rat Genome Database

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Variant: RGD:151734831 -  Homo sapiens

RGD ID: 151734831
RS ID: rs868081502
ClinVar ID: CV1494060
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C9  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 39,306,901
GRCh38 5 39,306,799
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001737.5:c.1241-7T>A
LRG_32:g.62755T>A
NG_009894.1:g.62755T>A
NC_000005.10:g.39306799A>T
More... 		10/05/2022 intron variant likely benign|uncertain significance none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:C9
Accession:NM_001737
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001984587 CLINVAR
  RCV003941216 CLINVAR
dbSNP (RS) rs868081502 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C9 CLINVAR
OMIM 120940 CLINVAR