RGD:156002146 Rat Genome Database

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Variant: RGD:156002146 -  Homo sapiens

RGD ID: 156002146
ClinVar ID: CV2014803
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMEM199  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 26,687,535
GRCh38 17 28,360,512
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_152464.3:c.376-17C>T
NG_046803.1:g.7932C>T
NC_000017.11:g.28360512C>T
NC_000017.10:g.26687535C>T
 05/20/2023 intron variant likely benign none provided

Gene Symbol:TMEM199
Accession:NM_152464
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002690108 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TMEM199 CLINVAR
OMIM 616815 CLINVAR