RGD:156144123 Rat Genome Database

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:

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

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 NP_114404.1:p.Ser319Leu More...	09/27/2021	missense variant	uncertain significance	AllHighlyPenetrant

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*

ClinVar GRCh37	ClinVar GRCh38

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