Variant #0000720469 (NC_000005.9:g.60448723G>A, NM_174889.4:c.451G>A (NDUFAF2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.60448723G>A
DNA change (hg38) -
Published as NDUFAF2(NM_174889.4):c.451G>A (p.G151S), NDUFAF2(NM_174889.5):c.451G>A (p.G151S)
ISCN -
DB-ID NDUFAF2_000003 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00461 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMIM15 NM_001048249.3 -?/. - c.*7051C>T r.(=) p.(=)
NDUFAF2 NM_174889.4 -?/. - c.451G>A r.(?) p.(Gly151Ser)


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