Variant #0000727607 (NC_000020.10:g.13769298G>C, NM_024120.4:c.327G>C (NDUFAF5))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.13769298G>C
DNA change (hg38) -
Published as NDUFAF5(NM_024120.4):c.327G>C (p.K109N)
ISCN -
DB-ID NDUFAF5_000007 See all 3 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) 0.00045 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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESF1 NM_016649.3 ?/. - c.-3874C>G r.(?) p.(=)
NDUFAF5 NM_024120.4 ?/. - c.327G>C r.(?) p.(Lys109Asn)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.