Variant #0000296398 (NC_000011.9:g.67800633G>A, NM_002496.3:c.255G>A (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.67800633G>A
DNA change (hg38) g.68033166G>A
Published as NDUFS8(NM_002496.3):c.255G>A (p.P85=), NDUFS8(NM_002496.4):c.255G>A (p.P85=)
ISCN -
DB-ID NDUFS8_000003 See all 2 reported entries
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) 0.00324 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH3B1 NM_000694.2 -?/. - c.*5227G>A r.(=) p.(=)
NDUFS8 NM_002496.3 -?/. - c.255G>A r.(?) p.(Pro85=)


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