Variant #0000508126 (NC_000001.10:g.63063676_63063679del, NC_000001.10(NM_033407.2):c.1683-11376_1683-11373del (DOCK7))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.63063676_63063679del |
| DNA change (hg38) |
g.62598005_62598008del |
| Published as |
ANGPTL3(NM_014495.4):c.439_442delAACT (p.N147*), DOCK7(NM_001271999.2):c.1683-11376_1683-11373delAGTT |
| ISCN |
- |
| DB-ID |
ANGPTL3_000034 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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