Variant #0000441213 (NC_000017.10:g.4837220_4837258del, NM_000173.5:c.1321_1359del (GP1BA))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.4837220_4837258del |
| DNA change (hg38) |
g.4933925_4933963del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GP1BA_000005 See all 15 reported entries |
| Variant remarks |
reference C-allele (2 repeat units SEPAPSPTTPEPT) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-12-21 17:24:28 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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