Variant #0000577229 (NC_000023.10:g.70361160_70361171dup, NM_005120.2:c.6348_6359dup (MED12))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.70361160_70361171dup |
| DNA change (hg38) |
g.71141310_71141321dup |
| Published as |
MED12(NM_005120.2):c.6348_6359dup (p.(His2116_Gln2119dup)), MED12(NM_005120.2):c.6348_6359dupCCAGCAGCAACA (p.H2116_Q2119dup), MED12(NM_005120.3):c.... |
| ISCN |
- |
| DB-ID |
MED12_000118 See all 4 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_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 |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|