Variant #0000621488 (NC_000005.9:g.140027138C>G, NM_002488.4:c.31G>C (NDUFA2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140027138C>G
DNA change (hg38) g.140647553C>G
Published as NDUFA2(NM_001185012.1):c.31G>C (p.G11R)
ISCN -
DB-ID IK_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) 0.00012 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.31G>C r.(?) p.(Gly11Arg)
IK NM_006083.3 -?/. - c.-356C>G r.(?) p.(=)
TMCO6 NM_018502.3 -?/. - c.*2455C>G r.(=) p.(=)


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