RGD:11659559 Rat Genome Database

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Variant: RGD:11659559 -  Homo sapiens

RGD ID: 11659559
RS ID: rs886049566
ClinVar ID: CV333165
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC11A2  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 51,385,374
GRCh38 12 50,991,591
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_021139.1:g.41685T>A
NC_000012.12:g.50991591A>T
NC_000012.11:g.51385374A>T
LRG_1160t4:c.1421+8T>A
More... 		06/14/2016 intron variant uncertain significance infancy <1 / 1 000 000 Anemia, hypochromic microcytic, with iron overload 1
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC11A2
Accession:NM_000617
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001379448
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001174127
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001174128
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001174129
Location:INTRON

Gene Symbol:SLC11A2
Accession:XM_047428887
Location:INTRON

Gene Symbol:SLC11A2
Accession:XM_011538404
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001414745
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001379447
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001174125
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001379446
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001414747
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001414746
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001414749
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001414744
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001414748
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001414750
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001174126
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001174130
Location:INTRON

Gene Symbol:SLC11A2
Accession:XM_011538405
Location:INTRON

Gene Symbol:SLC11A2
Accession:NM_001379455
Location:INTRON

Gene Symbol:SLC11A2
Accession:NR_183175
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_033421
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:XR_001748720
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:XR_944555
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_183176
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_166669
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_166670
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:XR_007063077
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_166668
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:XR_007063079
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:XR_007063078
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:XR_429104
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_183177
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_033422
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_183178
Location:INTRON;NON-CODING

Gene Symbol:SLC11A2
Accession:NR_183179
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000359227 CLINVAR
dbSNP (RS) rs886049566 CLINVAR
MedGen C3806153 CLINVAR
NCBI Gene SLC11A2 CLINVAR
OMIM 206100 CLINVAR
  600523 CLINVAR