RGD:11546537 Rat Genome Database

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Variant: RGD:11546537 -  Homo sapiens

RGD ID: 11546537
RS ID: rs144857384
ClinVar ID: CV257659
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYH9  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 22 36,723,483
GRCh38 22 36,327,438
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_567:g.65581A>G
NG_011884.2:g.65581A>G
NC_000022.11:g.36327438T>C
NC_000022.10:g.36723483T>C
More... 		05/30/2020 intron variant likely benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:MYH9
Accession:NM_002473
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000246590 CLINVAR
  RCV001589257 CLINVAR
dbSNP (RS) rs144857384 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene MYH9 CLINVAR
OMIM 160775 CLINVAR