Variant #0000984896 (NC_012920.1:m.14279G>A, NC_012920.1(ATP6_v001):c.*5072G>A (MT-ATP6))
Chromosome |
M |
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) |
m.14279G>A |
DNA change (hg38) |
- |
Published as |
MT-ND6(ENST00000361681.2):c.395C>T (p.(Ser132Leu)) |
ISCN |
- |
DB-ID |
MT-CO1_000008 |
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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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