Variant #0000172144 (NC_000003.11:g.15686425G>A, NM_000060.2:c.1062G>A (BTD))
| Chromosome |
3 |
| Allele |
Paternal (confirmed) |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15686425G>A |
| DNA change (hg38) |
g.15644918G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BTD_000110 See all 2 reported entries |
| Variant remarks |
normal BTD activity in parent, probable in index |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
rare |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.0005 View details |
| Owner |
Jasper Saris |
| Database submission license |
No license selected |
| Created by |
Jasper Saris |
| Date created |
2011-01-17 13:52:00 +01:00 (CET) |
| Date last edited |
2011-01-17 22:59:00 +01:00 (CET) |

Variant on transcripts
Screenings
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