RGD:11629705 Rat Genome Database

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Variant: RGD:11629705 -  Homo sapiens

RGD ID: 11629705
ClinVar ID: CV352233
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF674  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 46,358,811
GRCh38 X 46,499,376
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_023376.1:g.51082A>G
NC_000023.11:g.46499376T>C
NC_000023.10:g.46358811T>C
NM_001039891.3:c.*467A>G
More... 		06/14/2016 3 prime utr variant benign Mental retardation, nonsyndromic, X-linked; X-linked non-specific intellectual disability

Variant Details
Variant Transcripts
Gene Symbol:ZNF674
Accession:NM_001039891
Location:3UTRS;EXON

Gene Symbol:ZNF674
Accession:NM_001146291
Location:3UTRS;EXON

Gene Symbol:ZNF674
Accession:XM_011543943
Location:3UTRS;EXON

Gene Symbol:ZNF674
Accession:NM_001190417
Location:3UTRS;EXON

Variant Samples