RGD:11605869 Rat Genome Database

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Variant: RGD:11605869 -  Homo sapiens

RGD ID: 11605869
RS ID: rs778566330
ClinVar ID: CV315560
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: VPS13B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 100,889,239
GRCh38 8 99,877,011
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
LRG_351t1:c.*1345C>T
LRG_351:g.868746C>T
NG_007098.2:g.868746C>T
NC_000008.11:g.99877011C>T
More... 		01/12/2018 3 prime utr variant uncertain significance infancy Cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness; Pepper syndrome
Disease Annotations     Click to see Annotation Detail View
Cohen syndrome  (IAGP)


Variant Details
Variant Transcripts
Gene Symbol:VPS13B
Accession:NM_152564
Location:3UTRS;EXON

Gene Symbol:VPS13B
Accession:NM_017890
Location:3UTRS;EXON

Gene Symbol:VPS13B
Accession:NM_181661
Location:INTRON

Gene Symbol:VPS13B
Accession:NM_015243
Location:INTRON

Gene Symbol:VPS13B
Accession:NR_047582
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000324633 CLINVAR
dbSNP (RS) rs778566330 CLINVAR
MedGen C0265223 CLINVAR
NCBI Gene VPS13B CLINVAR
OMIM 216550 CLINVAR
  607817 CLINVAR
SNOMED CT 56604005 CLINVAR