Variant #0000053091 (NC_000023.10:g.29959810_29959816del, NM_014271.3:c.1100_1106del (IL1RAPL1))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.29959810_29959816del |
| DNA change (hg38) |
g.29941693_29941699del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
IL1RAPL1_000015 See all 2 reported entries |
| Variant remarks |
cDNA expression cloning HEK293 shows mislocalized protein (cytoplasm in cell surface), no rescue increased number/length neurite outgrowths |
| Reference |
PubMed: Piton 2008, Journal: Piton 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| 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 |
2015-01-25 16:26:23 +01:00 (CET) |
| Date last edited |
2020-07-17 21:27:50 +02:00 (CEST) |

Variant on transcripts
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