RGD:11656153 Rat Genome Database

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Variant: RGD:11656153 -  Homo sapiens

RGD ID: 11656153
RS ID: rs886060469
ClinVar ID: CV303436
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC34A1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 176,825,610
GRCh38 5 177,398,609
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016223.1:g.19179G>A
NC_000005.10:g.177398609G>A
NC_000005.9:g.176825610G>A
NM_003052.5:c.*323G>A
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


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

Gene Symbol:SLC34A1
Accession:NM_003052
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:SLC34A1
Accession:NM_001167579
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000331124 CLINVAR
dbSNP (RS) rs886060469 CLINVAR
MedGen C2676786 CLINVAR
NCBI Gene SLC34A1 CLINVAR
OMIM 182309 CLINVAR
  612286 CLINVAR