Variant #0000569894 (NC_000020.10:g.47601338_47601345dup, NM_006420.2:c.2031_2038dup (ARFGEF2))
| Chromosome |
20 |
| 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.47601338_47601345dup |
| DNA change (hg38) |
g.48984801_48984808dup |
| Published as |
ARFGEF2(NM_006420.2):c.2031_2038dupCATAGCCC (p.Q680Pfs*2) |
| ISCN |
- |
| DB-ID |
ARFGEF2_000061 |
| 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 |
2020-07-16 18:00:56 +02:00 (CEST) |

Variant on transcripts
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