Variant #0000680610 (NC_000016.9:g.57485080dup, NM_020312.3:c.202dup (COQ9))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57485080dup
DNA change (hg38) -
Published as COQ9(NM_020312.3):c.202dupG (p.A68Gfs*5)
ISCN -
DB-ID CIAPIN1_000011
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COQ9 NM_020312.3 +?/. - c.202dup r.(?) p.(Ala68GlyfsTer5)
CIAPIN1 NM_020313.2 +?/. - c.-3878dup r.(?) p.(=)


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