Variant #0000557663 (NC_000016.9:g.24801564_24801565del, NM_014494.2:c.1601_1602del (TNRC6A))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.24801564_24801565del |
| DNA change (hg38) |
g.24790243_24790244del |
| Published as |
TNRC6A(NM_014494.2):c.1600_1601del (p.(Cys534PhefsTer4)) |
| ISCN |
- |
| DB-ID |
TNRC6A_000003 |
| 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-09 14:23:15 +02:00 (CEST) |

Variant on transcripts
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