RGD:405279989 Rat Genome Database

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Variant: RGD:405279989 -  Homo sapiens

RGD ID: 405279989
ClinVar ID: CV3191560
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEMF  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 50,312,992
GRCh38 14 49,846,274
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001301732.3:c.232-9T>C
NM_004713.6:c.232-9T>C
NG_051075.2:g.11514T>C
NG_051075.1:g.11930T>C
More... 		05/01/2019 intron variant benign NEMF-related condition

Gene Symbol:NEMF
Accession:XM_011537317
Location:INTRON

Gene Symbol:NEMF
Accession:NM_004713
Location:INTRON

Gene Symbol:NEMF
Accession:NM_001301732
Location:INTRON

Gene Symbol:NEMF
Accession:XM_047431912
Location:INTRON

Gene Symbol:NEMF
Accession:XM_017021761
Location:INTRON

Gene Symbol:NEMF
Accession:XM_011537318
Location:INTRON

Gene Symbol:NEMF
Accession:XM_047431911
Location:INTRON

Gene Symbol:NEMF
Accession:XR_943557
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV003919710 CLINVAR
NCBI Gene NEMF CLINVAR
OMIM 608378 CLINVAR