Variant #0000560314 (NC_000017.10:g.14110489C>T, NM_001303.3:c.1291C>T (COX10))

Chromosome 17
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.14110489C>T
DNA change (hg38) g.14207172C>T
Published as COX10(NM_001303.3):c.1291C>T (p.R431W, p.(Arg431Trp)), COX10(NM_001303.4):c.1291C>T (p.R431W)
ISCN -
DB-ID COX10_000018 See all 4 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) 0.00289 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX10 NM_001303.3 ?/. - c.1291C>T r.(?) p.(Arg431Trp)


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