Variant #0000296357 (NC_000012.11:g.4758305G>C, NM_005002.4:c.13G>C (NDUFA9))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4758305G>C
DNA change (hg38) g.4649139G>C
Published as NDUFA9(NM_005002.5):c.13G>C (p.A5P)
ISCN -
DB-ID NDUFA9_000001
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) 0.00216 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKAP3 NM_001278309.1 -/. - c.-639C>G r.(?) p.(=)
NDUFA9 NM_005002.4 -/. - c.13G>C r.(?) p.(Ala5Pro)


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