Variant #0000691700 (NC_000014.8:g.70793127G>A, NM_016468.6:c.244C>T (COX16))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70793127G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID COX16_000001 See all 2 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) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNJ2BP-COX16 NM_001202547.2 +/. - c.499C>T r.(?) p.(Arg167Ter)
COX16 NM_016468.6 +/. - c.244C>T r.(?) p.(Arg82Ter)
SYNJ2BP NM_018373.2 +/. - c.*46581C>T r.(=) p.(=)


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