Variant #0000508583 (NC_000001.10:g.92944348_92944351dup, NC_000001.10(NM_005263.3):c.925-8_925-5dup (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.92944348_92944351dup |
| DNA change (hg38) |
g.92478791_92478794dup |
| Published as |
GFI1(NM_001127215.1):c.925-7_925-6insCTCT (p.(=)), GFI1(NM_001127215.2):c.925-10_925-7dupCTCT, GFI1(NM_005263.3):c.925-10_925-7dupCTCT, GFI1(NM_00...) |
| ISCN |
- |
| DB-ID |
GFI1_000034 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) |
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 |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
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