RGD:28895454 Rat Genome Database

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Variant: RGD:28895454 -  Homo sapiens

RGD ID: 28895454
RS ID: rs753800840
ClinVar ID: CV880741
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WDR62  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 36,593,626
GRCh38 19 36,102,724
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_028101.1:g.52844G>T
NC_000019.9:g.36593626G>T
NM_001083961.1:c.3221-13G>T
NC_000019.10:g.36102724G>T
More... 		01/13/2018 intron variant uncertain significance MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH CORTICAL MALFORMATIONS; Primary autosomal recessive microcephaly 2
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:WDR62
Accession:XM_047438658
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438662
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438663
Location:INTRON

Gene Symbol:WDR62
Accession:XM_017026665
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526844
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438664
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526840
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438659
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001411146
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438665
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526841
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438660
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001083961
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438661
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001411147
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526842
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001411145
Location:INTRON

Gene Symbol:WDR62
Accession:NM_173636
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438666
Location:INTRON

Gene Symbol:WDR62
Accession:XM_005258809
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526843
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438657
Location:INTRON

Gene Symbol:WDR62
Accession:XR_001753672
Location:INTRON;NON-CODING

Gene Symbol:WDR62
Accession:XR_001753671
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001122468 CLINVAR
dbSNP (RS) rs753800840 CLINVAR
MedGen C1858535 CLINVAR
NCBI Gene WDR62 CLINVAR
OMIM 604317 CLINVAR
  613583 CLINVAR