Variant #0000980984 (NC_000014.8:g.70795927_70795928del, NM_016468.6:c.167_168del (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.70795927_70795928del
DNA change (hg38) -
Published as COX16(NM_016468.7):c.167_168del (p.(Leu56Glnfs*4))
ISCN -
DB-ID COX16_000002
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) 5.0E-5 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 2024-04-19 20:27:30 +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.422_423del r.(?) p.(Leu141Glnfs*4)
COX16 NM_016468.6 ?/. - c.167_168del r.(?) p.(Leu56Glnfs*4)
SYNJ2BP NM_018373.2 ?/. - c.*43780_*43781del r.(=) p.(=)


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