Variant #0000558598 (NC_000016.9:g.57485118C>G, NM_020312.3:c.240C>G (COQ9))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57485118C>G
DNA change (hg38) g.57451206C>G
Published as COQ9(NM_020312.3):c.240C>G (p.P80=)
ISCN -
DB-ID CIAPIN1_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) 0.00025 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 2020-07-09 16:47:11 +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.240C>G r.(?) p.(Pro80=)
CIAPIN1 NM_020313.2 -?/. - c.-3920G>C r.(?) p.(=)


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