Variant #0000608488 (NC_000003.11:g.3189683_3189690del, NM_182916.2:c.1150_1157del (TRNT1))
| 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.3189683_3189690del |
| DNA change (hg38) |
g.3147999_3148006del |
| Published as |
TRNT1(NM_182916.3):c.1150_1157delCCTCCATT (p.P384Sfs*6) |
| ISCN |
- |
| DB-ID |
CRBN_000011 |
| 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 |
2019-12-04 14:54:23 +01:00 (CET) |
| Date last edited |
2020-06-12 10:59:42 +02:00 (CEST) |

Variant on transcripts
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