Variant #0000805178 (NC_000011.9:g.47602156G>A, NM_004551.2:c.213G>A (NDUFS3))

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.47602156G>A
DNA change (hg38) -
Published as NDUFS3(NM_004551.2):c.213G>A (p.K71=)
ISCN -
DB-ID KBTBD4_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS3 NM_004551.2 -?/. - c.213G>A r.(?) p.(Lys71=)
KBTBD4 NM_016506.5 -?/. - c.-1806C>T r.(?) p.(=)
PTPMT1 NM_175732.2 -?/. - c.*8975G>A r.(=) p.(=)


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