Variant #0000622090 (NC_000008.10:g.68107747G>A, NM_024790.6:c.3585G>A (CSPP1))
| Chromosome |
8 |
| 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.68107747G>A |
| DNA change (hg38) |
g.67195512G>A |
| Published as |
CSPP1(NM_001363131.2):c.3519G>A (p.E1173=) |
| ISCN |
- |
| DB-ID |
ARFGEF1_000011 |
| 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) |
1.0E-5 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2020-06-23 20:22:48 +02:00 (CEST) |

Variant on transcripts
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