RGD:11631896 Rat Genome Database

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Variant: RGD:11631896 -  Homo sapiens

RGD ID: 11631896
ClinVar ID: CV348845
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF81  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 47,777,060
GRCh38 X 47,917,661
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.*1029G>T
NG_021266.1:g.85760G>T
NC_000023.11:g.47917661G>T
NC_000023.10:g.47777060G>T
 06/14/2016 3 prime utr variant uncertain significance 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_007137
Location:3UTRS;EXON

Gene Symbol:ZNF81
Accession:NM_001378152
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