Variant #0000518373 (NC_000003.11:g.15686693G>C, NM_000060.2:c.1330G>C (BTD))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15686693G>C |
| DNA change (hg38) |
g.15645186G>C |
| Published as |
BTD(NM_000060.2):c.1330G>C (p.(Asp444His)), BTD(NM_000060.4):c.1330G>C (p.D444H), BTD(NM_001281723.3):c.1270G>C (p.D424H), BTD(NM_001281723.4):c.12... |
| ISCN |
- |
| DB-ID |
BTD_000021 See all 84 reported entries |
| 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) |
0.03261 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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