Variant #0000895230 (NC_000020.10:g.13765954_13765969dup, NC_000020.10(NM_024120.4):c.222+18_222+33dup (NDUFAF5))

Chromosome 20
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.13765954_13765969dup
DNA change (hg38) -
Published as NDUFAF5(NM_001352407.2):c.-474+10_-474+25dupCGGGGCGGCGGGGCGG
ISCN -
DB-ID NDUFAF5_000009 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESF1 NM_016649.3 -?/. - c.-536_-521dup r.(?) p.(=)
NDUFAF5 NM_024120.4 -?/. - c.222+18_222+33dup r.(=) p.(=)


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