Variant #0000508590 (NC_000001.10:g.92948938C>T, NM_005263.3:c.107G>A (GFI1))
| Chromosome |
1 |
| 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.92948938C>T |
| DNA change (hg38) |
g.92483381C>T |
| Published as |
GFI1(NM_001127215.1):c.107G>A (p.(Ser36Asn)), GFI1(NM_005263.3):c.107G>A (p.S36N) |
| ISCN |
- |
| DB-ID |
GFI1_000026 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) |
0.03985 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2021-02-08 18:36:18 +01:00 (CET) |

Variant on transcripts
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