Variant #0000617267 (NC_000018.9:g.9117843_9117844del, NM_021074.4:c.62_63del (NDUFV2))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.9117843_9117844del
DNA change (hg38) g.9117845_9117846del
Published as NDUFV2(NM_021074.4):c.62_63delAT (p.H21Rfs*6)
ISCN -
DB-ID NDUFV2_000002
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) 8.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-14 16:31:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFV2 NM_021074.4 +/. - c.62_63del r.(?) p.(His21ArgfsTer6)


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