RGD:156144123 Rat Genome Database

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Variant: RGD:156144123 -  Homo sapiens

RGD ID: 156144123
ClinVar ID: CV2383904
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNF26  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 119,206,788
GRCh38 11 119,336,078
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032015.5:c.956C>T
NC_000011.10:g.119336078C>T
NC_000011.9:g.119206788C>T
NM_032015.3:c.956C>T
More... 		09/27/2021 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:RNF26
Accession:NM_032015
Location:EXON
Amino Acid Prediction: S to L (nonsynonymous)
Amino Acid Position: 319
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MEAVYLVVNGLGLVLDVLTLVLDLNFLLVSSLLASLAWLLAFVYNLPHTVLTSLLHLGRGVLLSLLALIEAVVRFTCGGL
QALCTLLYSCCSGLESLKLLGHLASHGALRSREILHRGVLNVVSSGHALLRQACDICAIAMSLVAYVINSLVNICLIGTQ
NLFSLVLALWDAVTGPLWRMTDVVAAFLAHISSSAVAMAILLWTPCQLALELLASAARLLASFVLVNLTGLVLLACVLAV
TVTVLHPDFTLRLATQALSQLHARPSYHRLREDVMRLSRLALGSEAWRRVWSRSLQLASWPNRGGAPGAPQGDPMRVFLV
RTRRQDTLPEAGRRSEAEEEEARTIRVTPVRGRERLNEEEPPGGQDPWKLLKEQEERKKCVICQDQSKTVLLLPCRHLCL
CQACTEILMRHPVYHRNCPLCRRGILQTLNVYL*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004231760 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RNF26 CLINVAR
OMIM 606130 CLINVAR