Variant #0000545414 (NC_000011.9:g.67799634A>C, NM_002496.3:c.16A>C (NDUFS8))

Chromosome 11
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.67799634A>C
DNA change (hg38) g.68032167A>C
Published as NDUFS8(NM_002496.3):c.16A>C (p.(Thr6Pro))
ISCN -
DB-ID ALDH3B1_000010
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 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     
ALDH3B1 NM_000694.2 -?/. - c.*4228A>C r.(=) p.(=)
NDUFS8 NM_002496.3 -?/. - c.16A>C r.(?) p.(Thr6Pro)


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