Variant #0000844505 (NC_012920.1:m.234G>A)

Individual ID 00406493
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.234G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID chrM_000088 See all 3 reported entries
Variant remarks -
Reference Journal: Liu 2022
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency heteroplasmy 0.044
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Liu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-03-31 11:14:37 +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


AscendingScreening ID     

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Genes screened     

Variants found     

Owner     
0000407736 DNA SEQ-NG-I buccal swab - - 1 Qi Liu


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