RGD:8690362 Rat Genome Database

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Variant: RGD:8690362 -  Homo sapiens

RGD ID: 8690362
RS ID: rs202043750
ClinVar ID: CV140310
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC113788297  NDUFAF6  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 96,037,206
GRCh38 8 95,024,978
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.10:g.96037206G>T
NC_000008.11:g.95024978G>T
NM_152416.2:c.-31G>T
NG_016647.2:g.134708G>T
More... 		02/04/2014 2kb upstream variant|5 prime utr variant|intron variant benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:NDUFAF6
Accession:NM_001354515
Location:5UTRS;INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354524
Location:5UTRS;INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354534
Location:5UTRS;INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354514
Location:5UTRS;INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354522
Location:5UTRS;INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354525
Location:5UTRS;INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354518
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_152416
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354527
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354528
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354516
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354530
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354521
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354532
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354529
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354531
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354519
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354533
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001330582
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NM_001354517
Location:INTRON

Gene Symbol:NDUFAF6
Accession:NR_148909
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148903
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148911
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148904
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148906
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148913
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148912
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148915
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148908
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148905
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148910
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148907
Location:INTRON;NON-CODING

Gene Symbol:NDUFAF6
Accession:NR_148914
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000124061 CLINVAR
dbSNP (RS) rs202043750 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene 113788297 CLINVAR
  NDUFAF6 CLINVAR
OMIM 612392 CLINVAR