rs1555581737 Rat Genome Database

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Variant: rs1555581737 -  Homo sapiens

RGD ID: 15203008
RS ID: rs1555581737
ClinVar ID: CV760545
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMEM199  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 26,686,435
GRCh38 17 28,359,412
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_152464.3:c.375+8C>T
NG_046803.1:g.6832C>T
NC_000017.11:g.28359412C>T
NC_000017.10:g.26686435C>T
More... 		03/29/2018 intron variant likely benign none provided

Gene Symbol:TMEM199
Accession:NM_152464
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV000913669 CLINVAR
dbSNP (RS) rs1555581737 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TMEM199 CLINVAR
OMIM 616815 CLINVAR