Variant #0000659056 (NC_000023.10:g.118222167_118222168del, NM_020721.1:c.3030_3031del (KIAA1210))
| Chromosome |
X |
| 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.118222167_118222168del |
| DNA change (hg38) |
g.119088204_119088205del |
| Published as |
KIAA1210(NM_020721.1):c.3030_3031delAG (p.R1010Sfs*31) |
| ISCN |
- |
| DB-ID |
KIAA1210_000035 |
| 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 |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-07-21 09:21:03 +02:00 (CEST) |

Variant on transcripts
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