Variant #0000504508 (NC_000001.10:g.196642977_196642978dup, NC_000001.10(NM_000186.3):c.245-10_245-9dup (CFH))
| 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.196642977_196642978dup |
| DNA change (hg38) |
g.196673847_196673848dup |
| Published as |
CFH(NM_000186.3):c.245-10_245-9dupTT (p.?), CFH(NM_000186.3):c.245-11_245-10dupTT, CFH(NM_000186.4):c.245-10_245-9dupTT |
| ISCN |
- |
| DB-ID |
CFH_000052 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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