Variant #0001042812 (NC_000019.9:g.19627142G>A, NC_000019.9(NM_015965.6):c.94+1G>A (NDUFA13))

Chromosome 19
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.19627142G>A
DNA change (hg38) -
Published as NDUFA13(NM_015965.7):c.94+1G>A
ISCN -
DB-ID NDUFA13_000003
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFA13 NM_015965.6 +?/. - c.94+1G>A r.spl? p.?
TSSK6 NM_032037.3 +?/. - c.-906C>T r.(?) p.(=)
YJEFN3 NM_198537.3 +?/. - c.-12600G>A r.(?) p.(=)


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