Variant #0000531588 (NC_000007.13:g.19156795_19156823del, NM_000474.3:c.123_151del (TWIST1))
| Chromosome |
7 |
| 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.19156795_19156823del |
| DNA change (hg38) |
g.19117172_19117200del |
| Published as |
TWIST1(NM_000474.3):c.123_151delCAGCAGGCGCAGCGCGGGCGGCGGCGCGG (p.S41Rfs*187) |
| ISCN |
- |
| DB-ID |
TWIST1_000065 |
| 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 |
2020-06-22 14:43:13 +02:00 (CEST) |

Variant on transcripts
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