Variant #0000443418 (NC_000016.9:g.17564818G>A, NM_022166.3:c.-165C>T (XYLT1))
| Chromosome |
16 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17564818G>A |
| DNA change (hg38) |
g.17470961G>A |
| Published as |
-403C>T |
| ISCN |
- |
| DB-ID |
XYLT1_000035 See all 3 reported entries |
| Variant remarks |
expression cloning luciferase promoter activity unchanged |
| Reference |
PubMed: Faust 2014 |
| ClinVar ID |
- |
| dbSNP ID |
rs118030014 |
| 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 |
2018-12-29 14:17:42 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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