Variant #0000657636 (NC_000015.9:g.66782113_66782116del, NC_000015.9(NM_002755.3):c.1068+12_1068+15del (MAP2K1))
| Chromosome |
15 |
| 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.66782113_66782116del |
| DNA change (hg38) |
g.66489775_66489778del |
| Published as |
MAP2K1(NM_002755.3):c.1068+12_1068+15delTATT, MAP2K1(NM_002755.4):c.1068+12_1068+15delTATT |
| ISCN |
- |
| DB-ID |
MAP2K1_000021 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_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|