Variant #0000001407 (NC_000004.11:g.74606024A>T, NM_000584.3:c.-352A>T (IL8))
| Individual ID |
00000161 |
| Chromosome |
4 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74606024A>T |
| DNA change (hg38) |
g.73740307A>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
IL8_000001 See all 4 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Hollegaard 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
45/197 cases |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Mads V Hollegaard |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2012-07-11 16:42:46 +02:00 (CEST) |
| Date last edited |
2019-10-27 12:56:34 +01:00 (CET) |

Variant on transcripts
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