RGD:156037608 Rat Genome Database

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Variant: RGD:156037608 -  Homo sapiens

RGD ID: 156037608
ClinVar ID: CV2239530
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNF26  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 119,205,929
GRCh38 11 119,335,219
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.97C>G
NC_000011.10:g.119335219C>G
NC_000011.9:g.119205929C>G
NM_032015.3:c.97C>G
More... 		10/12/2021 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:RNF26
Accession:NM_032015
Location:EXON
Amino Acid Prediction: L to V (nonsynonymous)
Amino Acid Position: 33
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MEAVYLVVNGLGLVLDVLTLVLDLNFLLVSSLVASLAWLLAFVYNLPHTVLTSLLHLGRGVLLSLLALIEAVVRFTCGGL
QALCTLLYSCCSGLESLKLLGHLASHGALRSREILHRGVLNVVSSGHALLRQACDICAIAMSLVAYVINSLVNICLIGTQ
NLFSLVLALWDAVTGPLWRMTDVVAAFLAHISSSAVAMAILLWTPCQLALELLASAARLLASFVLVNLTGLVLLACVLAV
TVTVLHPDFTLRLATQALSQLHARPSYHRLREDVMRLSRLALGSEAWRRVWSRSLQLASWPNRGGAPGAPQGDPMRVFSV
RTRRQDTLPEAGRRSEAEEEEARTIRVTPVRGRERLNEEEPPGGQDPWKLLKEQEERKKCVICQDQSKTVLLLPCRHLCL
CQACTEILMRHPVYHRNCPLCRRGILQTLNVYL*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004114530 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RNF26 CLINVAR
OMIM 606130 CLINVAR