Variant #0000518362 (NC_000003.11:g.15676984_15676990delinsTCC, NM_000060.2:c.98_104delinsTCC (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.15676984_15676990delinsTCC |
| DNA change (hg38) |
g.15635477_15635483delinsTCC |
| Published as |
BTD(NM_000060.4):c.98_104delGCGGCTGinsTCC (p.C33Ffs*36) |
| ISCN |
- |
| DB-ID |
BTD_000109 See all 5 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) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-12 12:15:45 +02:00 (CEST) |

Variant on transcripts
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