Variant #0000844457 (NC_012920.1:m.16399G>A)

Individual ID 00405097
Chromosome M
Allele Maternal (inferred)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) m.16399G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID chrM_000073 See all 2 reported entries
Variant remarks -
Reference Journal: Liu 2022
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency heteroplasmy 0.052
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Liu
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-03-31 11:00:14 +02:00 (CEST)
Date last edited 2022-04-23 18:56:43 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000406339 DNA SEQ-NG blood - MT-CO1, MT-CO2, MT-ND2, MT-ND5, MT-RNR2 7 Qi Liu


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