RGD:11590996 Rat Genome Database

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Variant: RGD:11590996 -  Homo sapiens

RGD ID: 11590996
RS ID: rs746946403
ClinVar ID: CV294172
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALB  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 74,286,029
GRCh38 4 73,420,312
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009291.1:g.21058A>C
NC_000004.12:g.73420312A>C
NC_000004.11:g.74286029A>C
NM_000477.5:c.*14A>C
More... 		06/14/2016 3 prime utr variant uncertain significance EUTHYROID HYPERTHYROXINEMIA 1
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ALB
Accession:NM_000477
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000324561 CLINVAR
dbSNP (RS) rs746946403 CLINVAR
MedGen C0342185 CLINVAR
NCBI Gene ALB CLINVAR
OMIM 103600 CLINVAR
  615999 CLINVAR