RGD:405049117 Rat Genome Database

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Variant: RGD:405049117 -  Homo sapiens

RGD ID: 405049117
ClinVar ID: CV3150823
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NDUFAF5  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 13,779,098
GRCh38 20 13,798,452
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_024120.5:c.480-9A>G
NM_001352403.2:c.9-9A>G
NG_015811.2:g.18426A>G
NG_015811.1:g.18427A>G
More...
11/13/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:NDUFAF5
Accession:NM_001352407
Location:5UTRS;INTRON

Gene Symbol:NDUFAF5
Accession:NM_001352406
Location:5UTRS;INTRON

Gene Symbol:NDUFAF5
Accession:XM_047440472
Location:5UTRS;INTRON

Gene Symbol:NDUFAF5
Accession:XM_047440473
Location:5UTRS;INTRON

Gene Symbol:NDUFAF5
Accession:NM_024120
Location:INTRON

Gene Symbol:NDUFAF5
Accession:NM_001039375
Location:INTRON

Gene Symbol:NDUFAF5
Accession:XM_006723624
Location:INTRON

Gene Symbol:NDUFAF5
Accession:XM_011529342
Location:INTRON

Gene Symbol:NDUFAF5
Accession:NM_001352403
Location:INTRON

Gene Symbol:NDUFAF5
Accession:NM_001352408
Location:INTRON

Gene Symbol:NDUFAF5
Accession:XM_047440469
Location:INTRON

Gene Symbol:NDUFAF5
Accession:XM_047440470
Location:INTRON

Gene Symbol:NDUFAF5
Accession:XM_047440471
Location:INTRON

Gene Symbol:NDUFAF5
Accession:NR_029377
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF5
Accession:XR_937140
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF5
Accession:NR_147983
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF5
Accession:NR_147982
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF5
Accession:NR_147981
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF5
Accession:NR_147979
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF5
Accession:NR_147978
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF5
Accession:NR_147980
Location:INTRON;NON-CODING

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PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003849427 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NDUFAF5 CLINVAR
OMIM 612360 CLINVAR