Variant #0000654180 (NC_000002.11:g.113890443G>A, NM_173841.2:c.538G>A (IL1RN))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.113890443G>A |
| DNA change (hg38) |
g.113132866G>A |
| Published as |
IL1RN(NM_001318914.1):c.427G>A (p.E143K), IL1RN(NM_001318914.2):c.427G>A (p.E143K), IL1RN(NM_173842.2):c.529G>A (p.(Glu177Lys)) |
| ISCN |
- |
| DB-ID |
IL1RN_000017 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) |
9.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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