Variant #0000571521 (NC_000022.10:g.22221726_22221728dup, NM_002745.4:c.20_22dup (MAPK1))
| Chromosome |
22 |
| 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.22221726_22221728dup |
| DNA change (hg38) |
g.21867436_21867438dup |
| Published as |
MAPK1(NM_002745.4):c.20_22dupCGG (p.A7dup), MAPK1(NM_002745.5):c.20_22dup (p.(Ala7dup)), MAPK1(NM_002745.5):c.20_22dupCGG (p.A7dup) |
| ISCN |
- |
| DB-ID |
MAPK1_000003 See all 3 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 |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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