RGD:11630948 Rat Genome Database

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Variant: RGD:11630948 -  Homo sapiens

RGD ID: 11630948
ClinVar ID: CV352264
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF41  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 47,327,111
GRCh38 X 47,467,712
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001324139.1:c.-186-11314A>G
NM_007130.3:c.-231A>G
NM_153380.3:c.-231A>G
NG_008238.1:g.20235A>G
More... 		06/14/2016 2kb upstream variant|5 prime utr variant benign Mental retardation, nonsyndromic, X-linked; X-linked non-specific intellectual disability

Variant Details
Variant Transcripts
Gene Symbol:ZNF41
Accession:XM_006724550
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_001324144
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_017029812
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_047442475
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_001324151
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_047442476
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_007130
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_001324148
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_047442474
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_006724555
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_017029811
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_001324150
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_047442479
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_153380
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_017029813
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_001324147
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:NM_001324152
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_047442472
Location:5UTRS;EXON

Gene Symbol:ZNF41
Accession:XM_047442480
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_017029810
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324142
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324143
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324153
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_017029815
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442482
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442484
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442471
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324141
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324145
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324139
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442483
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_017029814
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442477
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442473
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442481
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_047442478
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_017029816
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324149
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324140
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:XM_017029817
Location:5UTRS;INTRON

Gene Symbol:ZNF41
Accession:NM_001324157
Location:INTRON

Gene Symbol:ZNF41
Accession:NM_001324154
Location:INTRON

Gene Symbol:ZNF41
Accession:NM_001324155
Location:INTRON

Gene Symbol:ZNF41
Accession:NM_001324156
Location:INTRON

Variant Samples