Variant #0000817657 (NC_012920.1:g.?, MT-ND1(NC_012920.1(ND1_v001)):m.?)

Individual ID 00387644
Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
DNA change (hg38) g.?
Published as Mt deletion 4400 BP
ISCN -
DB-ID MT-ND1_000004
Variant remarks no protein change given, error in annotation, no mitochondrial gene/site indicated, mosaic
Reference PubMed: Zanolli 2020
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MT-ND1 NC_012920.1(ND1_v001) +?/. - m.? r.(?) p.(?)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000388870 DNA SEQ-NG blood targeted sequencing MT-ND1 1 LOVD