Variant #0001040067 (NC_000014.8:g.70809365T>C, NC_000014.8(NM_016468.6):c.141+10A>G (COX16))

Chromosome 14
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.70809365T>C
DNA change (hg38) -
Published as COX16(NM_016468.7):c.141+10A>G
ISCN -
DB-ID COX16_000003
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) 0.00015 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNJ2BP-COX16 NM_001202547.2 ?/. - c.397-13412A>G r.(=) p.(=)
COX16 NM_016468.6 ?/. - c.141+10A>G r.(=) p.(=)
SYNJ2BP NM_018373.2 ?/. - c.*30343A>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.