Variant #0000252072 (NC_000002.11:g.8877136A>G, NC_000002.11(NM_020738.2):c.3586-7T>C (KIDINS220))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.8877136A>G |
| DNA change (hg38) |
g.8737006A>G |
| Published as |
KIDINS220(NM_001348738.1):c.3529-7T>C, KIDINS220(NM_020738.2):c.3586-7T>C (p.(=)), KIDINS220(NM_020738.4):c.3586-7T>C |
| ISCN |
- |
| DB-ID |
KIDINS220_000006 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) |
0.00304 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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