Variant #0000477902 (NC_012920.1:m.8584G>A, NC_012920.1(ATP6_v001):c.58G>A (MT-ATP6))
| 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.8584G>A |
| DNA change (hg38) |
m.8584G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MT-ATP6_000003 |
| Variant remarks |
Variant Error [EBUILDMISMATCH]: This variant seems to mismatch; the genomic variants on hg19 and hg38 seem to not belong together. Please fix this entry and then remove this message. |
| Reference |
PubMed: International HapMap 3 Consortium2010 |
| ClinVar ID |
- |
| dbSNP ID |
rs3135028 |
| Origin |
Somatic |
| Segregation |
- |
| Frequency |
12/90 (0.120) |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Raúl Cuauhtémoc Baptista Rosas |
| Database submission license |
No license selected |
| Created by |
Raúl Cuauhtémoc Baptista Rosas |
| Date created |
2019-05-05 18:32:57 +02:00 (CEST) |
| Date last edited |
2019-05-22 19:49:56 +02:00 (CEST) |

Variant on transcripts
Screenings
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