RGD:405113266 Rat Genome Database

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Variant: RGD:405113266 -  Homo sapiens

RGD ID: 405113266
ClinVar ID: CV3133620
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYH9  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 36,723,492
GRCh38 22 36,327,447
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002473.6:c.518+14C>T
LRG_567:g.65572C>T
NG_011884.2:g.65572C>T
NC_000022.11:g.36327447G>A
More... 		04/25/2023 intron variant likely benign none provided

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

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003836413 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYH9 CLINVAR
OMIM 160775 CLINVAR