RGD:11662026 Rat Genome Database

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Variant: RGD:11662026 -  Homo sapiens

RGD ID: 11662026
RS ID: rs886058286
ClinVar ID: CV293743
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: THRB  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 24,162,470
GRCh38 3 24,120,979
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001354708.2:c.*1905A>G
NM_001354709.2:c.*1905A>G
NG_009159.1:g.378844A>G
NC_000003.12:g.24120979T>C
More... 		06/14/2016 3 prime utr variant uncertain significance HYPERTHYROXINEMIA, FAMILIAL EUTHYROID, SECONDARY TO PITUITARY AND PERIPHERAL RESISTANCE TO THYROID HORMONES
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:THRB
Accession:XM_047448801
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448816
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001252634
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354710
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001374827
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448796
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448811
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448791
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448807
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448792
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448815
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_011534047
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001374823
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448806
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_024453737
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448810
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448809
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354712
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001374822
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001374824
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448802
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448789
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448817
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001374825
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448798
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_011534050
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354709
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354715
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354713
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448790
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001374826
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448812
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448795
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_024453734
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448805
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448818
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448797
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448813
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001128176
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448814
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_000461
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001128177
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_017007113
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448799
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448800
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354708
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448794
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448803
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448793
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448808
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:XM_047448804
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354711
Location:3UTRS;EXON

Gene Symbol:THRB
Accession:NM_001354714
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000382083 CLINVAR
dbSNP (RS) rs886058286 CLINVAR
MedGen C2937288 CLINVAR
NCBI Gene THRB CLINVAR
OMIM 188570 CLINVAR
  190160 CLINVAR