Variant #0000549543 (NC_000012.11:g.95397380dup, NM_018838.4:c.83dup (NDUFA12))

Chromosome 12
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.95397380dup
DNA change (hg38) g.95003604dup
Published as NDUFA12(NM_001258338.1):c.83dup (p.(Arg29GlnfsTer4)), NDUFA12(NM_018838.5):c.76delGinsGT (p.R29Qfs*4)
ISCN -
DB-ID NDUFA12_000010 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
NDUFA12 NM_018838.4 ?/. - c.83dup r.(?) p.(Arg29GlnfsTer4)


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