Variant #0000680611 (NC_000016.9:g.57486843G>C, NM_020312.3:c.373G>C (COQ9))

Chromosome 16
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.57486843G>C
DNA change (hg38) -
Published as COQ9(NM_020312.3):c.373G>C (p.A125P), COQ9(NM_020312.4):c.373G>C (p.(Ala125Pro))
ISCN -
DB-ID CIAPIN1_000012 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) 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 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COQ9 NM_020312.3 ?/. - c.373G>C r.(?) p.(Ala125Pro)
CIAPIN1 NM_020313.2 ?/. - c.-5645C>G r.(?) p.(=)


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