Variant #0000689440 (NC_000005.9:g.140025253_140025254del, NM_002488.4:c.218_219del (NDUFA2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.140025253_140025254del
DNA change (hg38) -
Published as NDUFA2(NM_002488.5):c.218_219delAA (p.Q73Rfs*12)
ISCN -
DB-ID IK_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFA2 NM_002488.4 +?/. - c.218_219del r.(?) p.(Gln73ArgfsTer12)
IK NM_006083.3 +?/. - c.-2241_-2240del r.(?) p.(=)
TMCO6 NM_018502.3 +?/. - c.*570_*571del r.(=) p.(=)


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