Variant #0000334569 (NC_000023.10:g.70360663_70360668dup, NM_005120.2:c.6223_6228dup (MED12))
| 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.70360663_70360668dup |
| DNA change (hg38) |
g.71140813_71140818dup |
| Published as |
MED12(NM_005120.2):c.6207_6208insCAGCAG (p.?), MED12(NM_005120.3):c.6223_6228dupCAGCAG (p.Q2075_Q2076dup) |
| ISCN |
- |
| DB-ID |
MED12_000116 See all 2 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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