Variant #0000002378 (NC_000004.11:g.84185440A>G, COQ2(NM_015697.7):c.1178T>C)

Individual ID 00002378
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.84185440A>G
Reference Chen YP1, Zhao B1, Cao B1, Song W1, Guo X1, Wei QQ1, Yang Y2, Yuan LX3, Shang HF4.(2015)
DB-ID COQ2_000014 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00411 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
COQ2 NM_015697.7 ./. 7 c.1178T>C r.(?) p.(Val393Ala) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002378 ? ? COQ2 1 Y Yang