RGD:11631326 Rat Genome Database

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Variant: RGD:11631326 -  Homo sapiens

RGD ID: 11631326
ClinVar ID: CV348877
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF81  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 47,780,335
GRCh38 X 47,920,936
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_007137.3:c.*4304A>G
NG_021266.1:g.89035A>G
NC_000023.11:g.47920936A>G
NC_000023.10:g.47780335A>G
 06/14/2016 3 prime utr variant likely benign Mental retardation, nonsyndromic, X-linked; X-linked non-specific intellectual disability

Variant Details
Variant Transcripts
Gene Symbol:ZNF81
Accession:NM_001378153
Location:3UTRS;EXON

Gene Symbol:ZNF81
Accession:NM_001378152
Location:3UTRS;EXON

Gene Symbol:ZNF81
Accession:NM_007137
Location:3UTRS;EXON

Gene Symbol:ZNF81
Accession:NM_001378154
Location:INTRON

Gene Symbol:ZNF81
Accession:NM_001378155
Location:INTRON

Gene Symbol:ZNF81
Accession:NR_165431
Location:INTRON;NON-CODING

Variant Samples