Variant #0000675457 (NC_000001.10:g.1470999C>G, ATAD3A(NM_018188.3):c.*1547C>G)
Chromosome |
1 |
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) |
g.1470999C>G |
DNA change (hg38) |
- |
Published as |
TMEM240(NM_001114748.1):c.343G>C (p.V115L) |
ISCN |
- |
DB-ID |
ATAD3A_000056 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (large NGS studies) |
1.0E-5 View details |
Owner |
VKGL-NL_AMC |

Variant on transcripts
|
|