RGD:11615677 Rat Genome Database

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Variant: RGD:11615677 -  Homo sapiens

RGD ID: 11615677
RS ID: rs544474028
ClinVar ID: CV340994
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127829729  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 64,455,276
GRCh38 15 64,163,077
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_10t1:c.-91A>C
LRG_10:g.5079A>C
NG_012979.1:g.5079A>C
NC_000015.10:g.64163077T>G
More... 		01/13/2018 5 prime utr variant uncertain significance OI 9; Oi type IX; Osteogenesis imperfecta sillence type II/III without abnormality of type I collagen
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000287987 CLINVAR
dbSNP (RS) rs544474028 CLINVAR
MedGen C1850169 CLINVAR
NCBI Gene PPIB CLINVAR
OMIM 123841 CLINVAR
  259440 CLINVAR