RGD:150443117 Rat Genome Database

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Variant: RGD:150443117 -  Homo sapiens

RGD ID: 150443117
RS ID: rs55633261
ClinVar ID: CV1266345
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126863137  MYH9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 36,696,715
GRCh38 22 36,300,669
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.2838+182C>T
LRG_567:g.92350C>T
NG_011884.2:g.92350C>T
NC_000022.11:g.36300669G>A
More... 		07/31/2018 intron variant benign none provided

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001690781 CLINVAR
dbSNP (RS) rs55633261 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126863137 CLINVAR
  MYH9 CLINVAR
OMIM 160775 CLINVAR