RGD:156037608 Rat Genome Database

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:

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

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 NP_114404.1:p.Leu33Val More...	10/12/2021	missense variant	uncertain significance	AllHighlyPenetrant

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*

ClinVar GRCh37	ClinVar GRCh38

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