rs1032590657 Rat Genome Database

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Variant: rs1032590657 -  Homo sapiens

RGD ID: 28870858
RS ID: rs1032590657
ClinVar ID: CV869553
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126861465  MGP  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 15,034,353
GRCh38 12 14,881,419
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_023331.2:g.9501C>A
NC_000012.12:g.14881419G>T
NC_000012.11:g.15034353G>T
NM_000900.3:c.*720C>A
More... 		04/27/2017 3 prime utr variant uncertain significance Pulmonic stenosis brachytelephalangism and calcification of cartilages
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MGP
Accession:NM_001190839
Location:3UTRS;EXON

Gene Symbol:MGP
Accession:NM_000900
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001113773 CLINVAR
dbSNP (RS) rs1032590657 CLINVAR
MedGen C1855607 CLINVAR
NCBI Gene LOC126861465 CLINVAR
  MGP CLINVAR
OMIM 154870 CLINVAR
  245150 CLINVAR