Variant #0000951668 (NC_000023.10:g.119005501C>T, NM_004541.3:c.-374C>T (NDUFA1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.119005501C>T
DNA change (hg38) -
Published as RNF113A(NM_006978.3):c.76G>A (p.G26R)
ISCN -
DB-ID NDUFA1_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFA1 NM_004541.3 ?/. - c.-374C>T r.(?) p.(=)
RNF113A NM_006978.2 ?/. - c.76G>A r.(?) p.(Gly26Arg)


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