Variant #0000443412 (NC_000016.9:g.17564778_17564779insN[238], NM_022166.3:c.-126_-125insN[238] (XYLT1))
| Chromosome |
16 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17564778_17564779insN[238] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
XYLT1_000034 |
| Variant remarks |
error in reference sequence, missing 238 nucleotides (CGCCGCGCGGGCCAGGCGCCCGCCCCTCCCTGCGCGCCCCGTCCCCGAGCGCGCGCCCGGCGCCCCCCTCCGCGGCCTCCCCGCTCCCGCCTCCCGCCTTCTCCTCCTCCTGGTGACGTCCGGGTCCCTGCCCGTCTGAAAACTCCGCGCCGCGGCGGTGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGAGGAGGAGCAGCGGCGAGCCGAGGCGGCG) |
| Reference |
PubMed: Faust 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| 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 13:26:53 +01:00 (CET) |
| Date last edited |
2021-12-15 22:04:31 +01:00 (CET) |

Variant on transcripts
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