Variant #0000909189 (NC_000016.9:g.2011195T>C, NM_004548.2:c.172T>C (NDUFB10))

Chromosome 16
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.2011195T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID NDUFB10_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs746790349
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-12-23 14:50:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFB10 NM_004548.2 ?/. - c.172T>C r.(?) p.(Tyr58His)


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